Bleach Solution Research Articles

First report of leaf spot caused by Paramyrothecium roridum on Coffea arabica in Hawai'i, USA.

During the 2022-2023 season, the harvested coffee crop in Hawai'i (Coffea arabica) was valued at $57.1 million (USDA NASS 2023). In September 2022, coffee leaf samples with foliar leaf spots affecting the Kona Typica variety were collected from Hōnaunau, Hawai'i, incidence <10%. The symptoms were circular, necrotic leaf spots with yellow margins, which merged, resulting in complete leaf blade coverage and subsequent leaf drop. Sporodochia were present on the abaxial leaf surface. Symptomatic leaf tissue was disinfected in 10% bleach solution for 60 seconds and chlorotic leaf tissue from the spot margins were excised and placed onto water agar and potato dextrose agar (PDA; Difco, USA). After a 7-day incubation period, pure cultures with white aerial mycelium having sporodochia arranged in concentric rings with olivaceous to black conidial masses were isolated. The conidia were aseptate, hyaline, smooth, cylindrical with rounded ends, measuring 5.1 to 6.8 μm long and 1.7 to 2.3 μm wide (n=50). Based on symptomology and cultural/morphological characteristics (Huaman-Pilco et al. 2023; Lombard et al. 2016; Pelayo-Sanchez et al. 2017), the isolates were initially identified as Paramyrothecium roridum (Tode) L. Lombard & Crous, comb. nov. (syn. Myrothecium roridum Tode). Fungal identification of isolate P22-81-2 was further confirmed using BLAST analysis of bulk sequenced PCR products of the ribosomal DNA internal transcribed spacer (ITS) region (White et al. 1990), β-tubulin (βtub), RNA polymerase II (RPB2), and calmodulin genes (Lombard et al., 2016; Huaman-Pilco et al., 2023). The gene sequences (GenBank accession nos. PP211198, PQ192517-19) were >98.4% identical to the P. roridum type specimen (CBS 357.89). A multilocus maximum likelihood phylogenetic analysis incorporating sequence data from previous relevant studies (Lombard et al., 2016; Pinruan et al. 2022) confirmed species identification. To prove pathogenicity, four, 26-month-old Kona Typica variety seedlings were foliar inoculated with a 1 X 106 conidia/ml suspension using a perfume atomizer. An additional four plants were inoculated in a similar manner with sterile water which served as controls. All plants were sprayed to drip on both the upper and lower leaf surfaces and incubated in a clear plastic bag to keep the humidity levels between 90 to 100% for 48 hours at 24°C. After 48 hours, the plants were removed from the bags, placed on a greenhouse bench, and observed weekly for symptom development. Within seven days light brown sunken spots had developed on all inoculated plants. The spots continued to enlarge having a dark distinct margin, light tan center, chlorotic halo, and formed concentric rings, which were identical to the original diseased samples. Leaf spots were not present on any of the control plants. The test was conducted twice. A fungus was consistently reisolated from the leaf spot margins of inoculated plants and morphologically (PDA) and molecularly (ITS, βtub, RPB2, calmodulin) identified as P. roridum, thus fulfilling Koch's Postulates. To the best of our knowledge, this is the first report of P. roridum causing leafspots on C. arabica plants in Hawai'i. This pathogen has been reported on coffee in other parts of the world including Colombia, Costa Rica, Guatemala, Puerto Rico, and Mexico (USDA Fungus-Host Database). Under the right conditions, P. roridum has the potential to cause leafspots and defoliation resulting in economic losses for coffee growers in Hawai'i.

Dehydration in Water: A Reagentless and Straightforward Synthesis of Tetrahydroquinazolines under Microwave Irradiation or by Stirring at Room Temperature, and Their Subsequent Conversion into Quinazolines in a Micellar Medium

AbstractUsing a reagent- and catalyst-free approach, a series of 2-substituted 1,2,3,4-tetrahydroquinazolines is synthesized by cyclocondensation between aldehydes and 2-aminobenzylamines via dehydration in water. The reactions are complete in 2 minutes under microwave irradiation and proceed well under stirring at room temperature, affording tetrahydroquinazolines in high to excellent yields. The products are water-insoluble and are isolated by simple filtration, avoiding a conventional work-up step and offering an organic-solvent-free process. Furthermore, the tetrahydroquinazolines are efficiently oxidized in a micellar medium derived from cetyltrimethylammonium bromide (CTAB) using a cheap commercial bleaching solution (4% NaOCl in water) to give quinazolines in high yields. This sustainable protocol has a near zero E-factor.

Fast, Easy, and Comprehensive Techniques for Microscopic Observations of Fungal and Oomycete Organisms Inside the Roots of Herbaceous and Woody Plants.

The roots of herbaceous and woody plants growing in soil are complex structures that are affected by both natural and artificial fungal colonization to various extents. To obtain comprehensive information about the overall distribution of fungi or oomycetes inside a plant root system, rapid, effective, and reliable screening methods are required. To observe both fine roots, i.e., a common site for penetration of fungi and oomycetes, and mature roots, different techniques are required to overcome visual barriers, such as root browning or tissue thickening. In our protocol, we propose using fast, cost-effective, and non-harmful methods to localize fungal or oomycete structures inside plant roots. Root staining with a fluorescent dye provides a quick initial indication of the presence of fungal structures on the root surfaces. The protocol is followed by clearing and staining steps, resulting in a deeper insight into the root tissue positioning, abundance, and characteristic morphological/reproductive features of fungal or oomycete organisms. If required, the stained samples can be prepared by using freeze-drying for further observations, including advanced microscopic techniques. Key features • The protocol enhances tissue-clearing techniques employing KOH or NaOH and is applicable to a broad range of roots from different plant species. • Hydroxides are mixed with hydrogen peroxide to obtain an efficient bleaching solution, which effectively clears roots without causing significant tissue damage. • The protocol could also be used for staining of fungi or oomycetes localized both on the root surface or inside the root tissues. • Simple combination of non-fluorescent methyl blue and fluorescent solophenyl flavine dyes allows the observation of fungal organisms in both brightfield and fluorescence microscopy.

Synergistic effects of using sodium hypochlorite (bleach) and desiccation in surface inactivation for Toxocara spp

Toxocara cati and T. canis are parasitic nematodes found in the intestines of cats and dogs respectively, with a cosmopolitan distribution, and the potential for anthropozoonotic transmission, resulting in human toxocariasis. Spread of Toxocara spp. is primarily through the ingestion of embryonated eggs contaminating surfaces or uncooked food, or through the ingestion of a paratenic host containing a third-stage larva. The Toxocara spp. eggshell is composed of a lipid layer providing a permeability barrier, a chitinous layer providing structural strength, and thin vitelline and uterine layers, which combined create a biologically resistant structure, making the Toxocara spp. egg very hardy, and capable of surviving for years in the natural environment. The use of sodium hypochlorite, household bleach, as a disinfectant for Toxocara spp. eggs has been reported, with results varying from ineffective to limited effectiveness depending on parameters including contact time, concentration, and temperature. Desiccation or humidity levels have also been reported to have an impact on larval development and/or survival of Toxocara spp. eggs. However, to date, after a thorough search of the literature, no relevant publications have been found that evaluated the use of sodium hypochlorite and desiccation in combination. These experiments aim to assess the effects of using a combination of desiccation and 10% bleach solution (0.6% sodium hypochlorite) on fertilized or embryonated eggs of T. cati, T. canis, and T. vitulorum. Results of these experiments highlight the synergistic effects of desiccation and bleach, and demonstrate a relatively simple method for surface inactivation, resulting in a decrease in viability or destruction of T. cati, T. canis and T. vitulorum eggs. Implications for these findings may apply to larger scale elimination of ascarid eggs from both research, veterinary, and farming facilities to mitigate transmission.

Efficacy Study of Eco-Friendly Bleaching Agent for Skeleton Preservation in Animal Skeleton

The currently used bleaching materials in skeletal preservation are hydrogen and carbamide peroxide materials with specific concentrations and techniques that impact environmental sustainability. This research describes a simple and eco-friendly technique for preserving skeletons. This research used a qualitative approach. Data were collected through observation and documentation. The collected data were analyzed descriptively. The results show that natural extracts, such as lemon combined with baking soda and commercial bleaching cloth agent, can bleach the skull and bone to preserve the skeleton. The commercial bleaching cloth agent is more capable of bleaching animal skulls and bones to preserve skeletons than natural extracts combined with baking soda do; however, the result is more brittle skeletons. Although specimens in lemon extract combined with baking soda solution more slowly clean and bleach skeleton than commercial bleaching solution, skeletal animals have bond strength and environment-friendly processes. This study recommends that an eco-friendly bleaching agent for skeletal preservation should be applied because it can cope with biological practices about osteology and other science subjects.

First report of bacterial leaf spot caused by Pseudomonas cichorii on Monstera adansonii in Hawai'i, USA.

Monstera adansonii is a popular ornamental house plant prized for its small size and unique leaf fenestrations. In Hawai'i, it is also sold as cut foliage (combined value ~$21K; USDA NASS 2019). In January 2022, yellow chlorotic lesions that progressed to greyish-black and, finally, to brown necrotic lesions were observed primarily along the margins of fenestrations on M. adansonii foliage at a plant nursery in Hilo, HI. All 100 variegated specimens in 4-inch pots were infected, exhibiting symptoms along the lighter yellowish-white margins. The green, unvariegated variety planted along a fence for cut foliage exhibited an infection rate of 10%. Symptomatic leaf tissue was disinfected for 1 minute in a 10% bleach solution. Tissue from the margins of leaf spots was subsequently dissected, soaked in sterile distilled water for 1 hour, and plated on Luria-Bertani (LB) agar. Plates contained nearly pure cream-colored bacterial colonies with undulate margins. Isolates were established from single colonies. One isolate (BCB001) was transferred to King's medium B (KMB) and culture fluorescence was observed under 365 nm UV light. Isolate BCB001, which was gram-negative, was identified as Pseudomonas cichorii based on the LOPAT scheme (Schaad et al. 2001). A partial 16S rRNA gene product (495 bp) using primers Y1/Y3 (Cruz et al. 2001) was sequenced and compared in GenBank (accession no. OQ875210) and was 100% identical to multiple accessions of P. cichorii in the NCBI database. Bacterial identity was further confirmed using the P. cichorii-specific primers Hrp1a/Hrp2a (Cottyn et al. 2011) to amplify and sequence a 790 bp fragment (accession no. OQ850761), which was identical to accession no. MH396007, a P. cichorii isolate recovered from Thai basil in Hawai'i. To prove pathogenicity, strain BCB001 was grown on LB agar for 48 h at 27°C and suspended in sterile water at 107-108 CFU/ml. Four healthy, 2-month-old unvariegated M. adansonii plants produced from cuttings were syringe inoculated following the protocol of Wang et al. (2022). Leaves were injected with sterile water using the same methods and acted as negative controls. Plants were placed in clear plastic bags and held at 24°C with 12 h light for 48 hours in a growth chamber, after which time the plants were removed from the bags and incubated under the same conditions for the remainder of the experiment. Leaf spots were not present on any of the control leaves or on noninjected leaves of the plants after five days of incubation. Grey to black, water-soaked leaf spots 0.84 - 15.24 mm in diameter were present on all injected leaves (96% of the injection sites) 2 days post-inoculation (DPI), which were identical to the original diseased samples. At 5 DPI, spots became dark brown to black with a yellow halo, and the affected tissue was completely collapsed. Bacterial colonies were consistently re-isolated from the lesion margins of inoculated plants and morphologically (LB and KMB) and molecularly (Hrp) identified as P. cichorii, thus fulfilling Koch's postulates. To the best of our knowledge, this is the first report of bacterial leaf spot caused by P. cichorii on M. adansonii in Hawai'i. Since M. adansonii is an ornamental plant that is prized for its leaves, leaf spots caused by P. cichorii can reduce the marketability of inventory. To avoid further spread, increasing plant spacing to improving airflow, decreasing the amount of watering, avoiding mist irrigation, and carefully removing and discarding diseased leaves are suggested.

Surface disinfection of wheat kernels using gas phase hydroxyl-radical processes: Effect on germination characteristics, microbial load, and functional properties.

Wheat kernels harbor a diverse microflora that can negatively affect the suitability of the grains for further processing. To reduce surface microflora, a kernel disinfection method is required that does not affect grain functionality. Three different versions of gas phase hydroxyl-radical processes were compared with the common method for grain disinfection, that is, a bleach treatment. The gas phase hydroxyl-radicals are generated by the UV-C mediated degradation of hydrogen peroxide and/or ozone in a near water-free process. It was found that treating kernels with a bleach solution could reduce total aerobic count (TAC) and fungal count to below the level of enumeration. In comparison, the gas phase hydroxyl-radical treatment, that is, H2 O2 -UV-ozone treatment, could support a 1.3 log count reduction (LCR) in TAC and a 1.1 LCR in fungal count. The microbial load reduction for the wholemeal samples was less pronounced as endophytic microorganisms were less affected by all treatments, hinting at a limited penetration depth of the treatments. Despite reducing the microbial load on the kernel surface through the bleach and H2 O2 -UV-ozone treatments, none of these treatments resulted in a reduced microbial count on grains that underwent sprouting after the treatments. No negative effect on germination power or development of the seedling was observed for any of the treatments. The gluten aggregation behavior and xylanase activity of the wholemeal also remained unchanged after the gas phase hydroxyl-radical treatments. Our findings suggest that UV-H2 O2 -ozone treatment shows promise for dry-kernel disinfection, but further optimization of the processing parameters is required.

Bleach Cleaning of Commercially Available Gold Nanopillar Arrays for Surface-Enhanced Raman Spectroscopy (SERS).

Surface-enhanced Raman spectroscopy (SERS) is a highly sensitive technique that can assist in trace analysis for biomedical, diagnostic, and environmental applications. However, a major limitation of SERS is surface contamination of the substrates used, which can complicate the spectral reproducibility, limits of detection, and detection of unknown analytes. This is especially prevalent with commercially available substrates as shipping under a controlled and clean environment is difficult. Here we report a method using dilute bleach solutions to remove surface contamination from commercially available substrates consisting of gold-coated nanopillar arrays that maintains functionality. The results show that this method can be used to remove background signals associated with typical surface contamination in commercially available substrates as well as remove thiolated self-assembled monolayers (SAMs). Results indicate the bleach oxidizes the surface contaminants, which can then be easily washed away. Although the metallic surface also becomes oxidized in this process, the surface can be reduced without loss of SERS activity. The SERS intensity of SAMs improved following bleach treatment across all concentrations studied.

Evaluation of a sequential anaerobic-aerobic membrane bioreactor system for treatment of traditional and insensitive munitions constituents

New energetic formulations containing insensitive high explosives (IHE), such as 2,4-dinitroanisole (DNAN), 3-nitro-1,2,4-triazole-5-one (NTO), and nitroguanidine (NQ) are being developed to provide safer munitions. The addition of IHE to munitions formulations results in complex wastewaters from explosives manufacturing, load and pour operations and demilitarization activities. New technologies are required to treat those wastewaters. The core objective of this research effort was to develop and optimize a dual anaerobic-aerobic membrane bioreactor (MBR) system for treatment of wastewater containing variable mixtures of traditional energetics, IHE, and anions. The combined system proved highly effective for treatment of traditional explosives (TNT, RDX, HMX), IHE (DNAN, NTO, NQ) and anions commonly used as military oxidants (ClO4−, NO3−). The anaerobic MBR, which was operated for more than 500 d, was observed to completely degrade mg L−1 concentrations of TNT, DNAN, ClO4− and NO3− under all operational conditions, including at the lowest hydraulic residence time (HRT) tested (2.2 d). The combined system generally resulted in complete treatment of mg L−1 concentrations of RDX and HMX to <20 μg L−1, with most of the degradation occurring in the anaerobic MBR and polishing in the aerobic system. No common daughter products of DNAN, TNT, RDX, or HMX were detected in the effluent. NTO was completely transformed in the anaerobic MBR, but residual 3-amino-1,2,4-triazole-5-one (ATO) was detected in system effluent. The ATO rapidly decomposed when bleach solution was added to the final effluent. NQ was initially recalcitrant in the system, but microbial populations eventually developed that could degrade >90% of the ∼10 mg L−1 NQ entering the anaerobic MBR, with the remainder degraded to <50 μg L−1 in the aerobic system. The dual MBR system proved to be capable of complete degradation of a wide mixture of munitions constituents and was resilient to changing influent composition.

First Report of Neofusicoccum australe Causing Branch Dieback of English Walnut cv. Chandler in Central Chile.

The English walnut (Juglans regia L.) is the second most important fruit crop of importance in Chile, with 43,700 hectares mainly in the Central Valley (www.odepa.cl, 2022). For several seasons symptoms of a branch dieback have been observed in walnut orchards with 3 to 50% of trees incidence levels. During the 2020 winter season (July) a total of 150 symptomatic spurs of 15 trees were sampled from an 8-year-old walnut cv. Chandler orchard located in Buin (33°42' S, 70° 42' W). The collected spurs showed external and internal brown necroses, starting from the tip with well-defined margins. The symptomatic tissue was cut in to small pieces (5 x 4 x 2 mm), surface disinfected by dipping in a 10% solution made from a commercial bleach solution (4,9% NaOHCl), rinsed twice in sterile water and plated on APDA (PDA Difco laboratories acidified with lactic acid (2,5 ml of 25% (vol/vol) per liter of medium). After five days at 20 °C in darkness, fast-growing, white-grey turning to black colonies were obtained, tentatively classified as a member of the Botryosphaeraceae family and two single-spore isolates (SS1, SS2) were selected for identification. Colony mycelia were first white and turned to light grey, dark grey or black, with tufts of mouse gray aerial mycelia. The pycnidia and conidia production was induced by inoculating autoclaved pine needles placed on APDA an incubation for 25 to 30 days at 20 °C in darkness. Black pycnidia solitary and globose were obtained producing hyaline, aseptate, fusiform to obovoid conidia with truncated ends with dimensions of (22.6-) 19.1 ± 1.4 (-13.3) x (6.7-) 5.5 ± 0.5 (-3.7) µm and 3.5 length/width ratio (n=100). Both isolates were identified using dichotomous keys confirming the description of Crous et al, 2006 as Neofusicoccum australe. The identification was molecularly confirmed by amplifying the nuclear ribosomal gene 5,8S (ITS1-5.8S-ITS2) using the ITS1/ITS4 primers, a partial region of β-tubulin gene (Bt2a/Bt2b), and the translation elongation factor 1-α gene (TEF1) with TEF1-728F/TEF1-986R primers. The BLASTn search revealed 100% of identity for ITS and TEF according to sequences of N. australe reference strains MT587467.1 and MK759852.1, respectively; and over 99% for β-tubulin compared to N. australe strain KX464929.1. The DNA sequences were submitted to the GenBank (ITS, OP142414, OP142416; BT, OP209981, OP209978; and TEF OP209979, OP209980) for SS1 and SS2 isolates, respectively, and deposited in the fungal collection of CChRGM - INIA, Chillán, Chile (RGM 3409 and 3410). Pathogenicity of both isolates was tested in 8-year-old asymtomatic English walnut cv. Chandler in the field during 2020 spring season, by cutting transversally 15 twigs of different tress and inoculating with a 5 day-old PDA plug. An equal number of wounded twigs were inoculated with a sterile PDA plug and served as control. After six months, all inoculated twigs developed the same necrotic lesions observed in field of 2.0 to 10.1 cm (SS1) and 1.9 to 10.8 cm (SS2) in length while control twigs showed only a scar without any dieback tissues. The inoculated pathogens of N. australe were recovered from the diseased tissues, thus fulfilling Koch's postulates. A similar dieback of walnut was reported in Chile, which caused Diplodia mutila (Díaz et al, 2018), and N. parvum (Luna et al, 2022) while N. australe has been reported in other hosts (Auger et al, 2013, Besoain et al, 2013). To the best of our knowledge, this is the first report of N. australe associated with walnut branch dieback in Chile.

First report of Curvularia leaf spot on Zea mays caused by Curvularia lunata in North Carolina.

In late July of 2022, corn leaves with spots were observed in a field at North Carolina State University's Vernon James Research and Extension Center (35.873294º N, 76.658599º W; Plymouth NC). The affected leaves contained small (two to three millimeters in diameter) tan-colored circular to oval lesions with reddish-brown margins and chlorotic haloes. The disease severity approached 50% on affected leaves. Leaf tissue from the margins of the lesions was excised and surface sterilized by soaking in 10 % bleach solution for two minutes followed by rinsing in distilled water. Next, leaf tissue was transferred to alkaline water agar amended with streptomycin (100 mgliter-1) and the plates were incubated at 27º C in dark. After one week, conidia were observed. Conidia were curved, light brown in color and contained three transverse septa. The size of the conidia (n= 30) ranged from 21-25 µm (average 24 µm) long by 7 to 10 µm wide (average 9 µm). These characteristics were typical of Curvularia lunata (Munkvold and White 2016). DNA from pure cultures was extracted, internal transcribed space region (ITS) was amplified using the primers ITS4 and ITS5 (White et al. 1990). Sequences were obtained and deposited into GenBank (accession no. OP998306). BLAST search indicated that the sequence was 100 % identical to C. lunata from Louisiana (MG 971305.1, Garcia- Aroca et al. 2018). Pathogenicity was confirmed on field corn cultivar 'Yellow dent' by inoculating two pots of two-week-old greenhouse-grown corn plants (6 plants per pot) by spraying conidial suspension with a concentration of 6 x 104 conidia /ml. The control plants (n= 6) were sprayed with distilled water and the plants were covered with a plastic bag for 24 hours. The plastic bags were removed and plants were moved to the greenhouse at 23º C. Four days after inoculation small round tan-colored lesions were observed and no symptoms on control plants. The experiment was repeated once and the pathogen was recovered from the symptomatic tissue. The morphology of the recovered isolate was similar to the original isolate. This is the first report of C. lunata causing leaf spot on corn in North Carolina. Although this disease has not been demonstrated to cause yield loss it has been detected more frequently in corn production areas of U.S. and should continue to be monitored going forward.

A sustainable low temperature combined pretreatment process for cotton assisted by ultraviolet-C radiation

The textile sector stands out as one of the largest consumers of water. Its significant usage of natural resources, energy, and water - particularly in wet processing - has deleterious effects on the environment. To mitigate the industry's ecological footprint, this investigation delves into the viability of pretreating cotton grey fabrics utilizing Ultraviolet-C radiation. An efficient Ultraviolet-C-assisted single-step process has been developed, combining desizing, scouring, and bleaching. The grey cotton fabric is padded with a bleaching solution and exposed under Ultraviolet-C followed by a low-temperature washing. The process parameters like time of exposure under Ultraviolet-C, the concentration of hydrogen peroxide, pH of the bleaching solution, and the temperature and duration of washing are optimized. The pretreated fabric is characterized by absorbency time, whiteness, strength, FTIR, WAXD, and SEM. The analysis of fabric structure using Fourier transform infrared spectroscopy and Wide-angle X-ray diffraction indicates no significant alterations in the parent structure of the fabric. The combined process saves 71% water, 73% time, and 70% energy from the conventional technique without compromising the quality of the fabric. The dyeability test reveals that the combined pretreatment can have a 42% higher dye uptake than the control. The life cycle analysis of the innovative one-step combined pretreatment reveals that it can potentially reduce over 60% of the environmental impacts associated with conventional processes, thereby promoting sustainability. Furthermore, since minimal modifications to existing setups are necessary, implementing this process within the textile industry is highly feasible.

First report of Neofusicoccum ribis causing stem blight and dieback of blueberry (Vaccinium corymbosum) in Michigan.

In July 2020, a 3-year-old 'Envoy' northern highbush blueberry bush (Vaccinium corymbosum L.) from a commercial farm in Van Buren County, Michigan was submitted to the Plant & Pest Diagnostics laboratory at Michigan State University. Field disease assessments across the 2-acre planting were an incidence of 2-5% and a severity of 50-100%. Symptoms included red shoot flagging and dead shoots retaining dry leaves, shoots with light green leaves and necrotic margins, and brown-black cankers at the base of the symptomatic shoots. Shoot sections displaying wood discoloration were surface disinfested by dipping in 95% ethanol and flame sterilized. The internal discolored tissues (0.5 cm2) were plated onto 1% ampicillin and streptomycin, quarter-strength potato dextrose agar (PDA) and incubated at room temperature until fungal colonies were observed. A fungus with rapid growth, developing white and then dark gray mycelium, resembling species in the family Botryosphaeriaceae was isolated and subcultured. After DNA extraction and amplification, sequences of three loci were obtained: the internal transcribed spacer (ITS) region, β-tubulin (Bt), and elongation factor 1-α (EF1) using primer pairs ITS1/ITS4, Bt2a/Bt2b, and EF1-728/EF1-986R, respectively (Slippers et al. 2004). The sequences showed 100% identity with Genbank numbers KF766205 (ITS region, 562 bp - OP588109), MT592721 (Bt, 436 bp - OP585548), and MT592229 (EF1, 306 bp - OP585547) of N. ribis (Slippers et al. 2013, Zhang et al. 2021). Sequences were identified using PopSet 1995604550 (Zhang et al. 2021). Pathogenicity was tested on 2-year-old 'Blueray' blueberries. Five plants, 3 shoots per plant (n = 15) were surface-sterilized with a 3% bleach solution by rinsing, wounded with razor blades using a scratching method in 'X' patterns across the length of the wound, and then inoculated using mycelium plugs (5 mm) from 7-day old cultures grown on full-strength PDA. Plugs were crushed and spread onto the wound and the wound was wrapped with parafilm. Control plant shoots (n = 9) were mock inoculated using sterile PDA plugs. Plants were maintained in the greenhouse at 23°C under a 14-hour photoperiod and imaged at 0-, 7-, and 12-days post inoculation (dpi). Symptoms began developing within 7 dpi. At 12 dpi, 9 of 15 inoculated shoots began displaying leaf necrosis and deep red or brown stem discoloration 6 cm above and below the wound, while controls remained healthy. Fungi morphologically identical to the original isolate were reisolated from sections taken from 2.5, 6.3, and 7 cm above and below the inoculation site. Species identity was confirmed by sequencing as described above. Neofusicoccum species are widespread and commonly associated with canker and dieback symptoms of blueberries (Flor et al. 2022). To our knowledge, this is the first report of stem blight and dieback caused by N. ribis in Michigan blueberry production. The species N. parvum and N. ribis have been reported on southern highbush blueberries in California (Koike et al. 2014) and Florida (Wright and Harmon 2010), but neither has been reported on blueberry in Michigan. Accurate diagnoses of Botryosphaeria fungal species in blueberries is critical for effective disease control and yield loss reduction.

Energetic Material Synthesis: Scale-up Using a Novel Modular Microflow Reactor Setup

The advantages of microflow reactors have proven to be manifold, e.g., the excellent cooling ability, which allows performing exothermic reactions like nitrations safely. A critical point remains the transition from gram scale to industrial production. On an industrial scale, they are often designed for specific syntheses and are therefore less useful for a conventional research laboratory. A reactor setup was successfully developed mitigating these shortcomings and allowing the use of highly corrosive materials, like fuming inorganic acids (e.g., nitric, sulfuric acid), bases (e.g., bleach solutions), and chlorinated solvents. As a proof of functionality, the synthesis of nitroguanidine has been performed on a lab scale and was significantly improved over reported batch syntheses in terms of safety and production rate. A scale-up to industrial scale has hence become feasible.

The use of white pomegranate extract as a bleaching material for hardness, roughness, and calcium levels in the enamel tooth

Background: Bleaching is the procedure of re-whitening teeth that have darkened to a shade near to their natural hue. Due to the unfavorable impact of chemical bleaching materials on enamel demineralization, the quest for natural bleaching solutions that have the same whitening effect while minimizing the negative consequences is encouraged. The punica granatum fruit is one of the natural components that can be employed. Purpose: This study aims to analyze the application of white pomegranate extract as an external bleach on the physical properties of the enamel surface of the tooth. Methods: thirty post-extraction bovine teeth were divided into treatment and control groups, then enamel surface hardness was measured using a Micro Vickers Hardness Tester, enamel surface roughness using a Surface Roughness test, and calcium levels using an EDS SEM tool before application of white pomegranate extract which is performed for 2 hours a day for two weeks. After two weeks, the enamel surface hardness, enamel surface roughness, and calcium levels were measured again. Results: The results of the treatment group using white pomegranate extract showed that there was no decrease in enamel surface hardness (p&gt;0.05), a decrease in enamel roughness (p&lt;0.05), and no decrease in calcium levels (p&gt;0.05). The control group's results using 16% carbamide peroxide showed a decrease in the hardness and surface roughness of the enamel, but it did not decrease the calcium content. Conclusion: white pomegranate extract can be used as an external bleaching agent because of not reduce the surface hardness, reduce the surface roughness and not reduced the calsium of the enamel tooth

Determining The Best Conditioning Method For Mammothred Daisy(Chrysanthemum Morifolium)

Background: Conditioning is a post-harvest step necessary in the maintenance of cut flowers. It not only helps to increase the shelf life of the cut flowers but also helps in increasing the time for which the flowers can be stored. The process of conditioning also helps in providing certain key nutrients to the cut flowers which are required for their sustainability. It also protects the flowers from getting contaminated by several disease-causing microbes. Most people usually do not pay enough attention to this process which often their beautiful and precious flowers to decay earlier than usual. Proper conditioning method can provide a solution to all these problems by providing optimum conditions for the flower and protects the cut flowers against early aging. Objective: The study was carried out with the objectives (1) to determine the best conditioning method for cut Mammoth Red Daisy flowers through scientific experiments and (2) to get views on the flowering behaviour under different conditions based on visual parameters. Methodology: This study's methodology combined experimental and observational research methods. The experiment was performed in the on-premises housekeeping lab at IHM Pusa, under the supervision of the research guide and lab attendant. Through the use of a Google Form-created questionnaire, the observational study was conducted. This questionnaire was filled out by subject experts in the domain based on the visual parameters from the experiment conducted. Results: Alittle contradictory from the expected, SET'A' was voted the best in visual parameters however the best conditioning method for the Mammoth Red Daisy was provided by SET 'C' from the experiment conducted which contained a solution of bleach, citric acid and sucrose, prepared in distilled water. Conclusion: According to the findings of the experiment and the observations made, it was found that the solution made in distilled water with bleach, citric acid, and sucrose proved to be the most effective in conditioning the Mammoth Daisy. Thus, it can be inferred that applying the aforementioned solution can significantly delay the early aging of cut flowers, lengthen their life, and aid in achieving sustainability.

The in vitro effect of solutions with or without sugar in dental bleaching

The interaction of bleaching technique (in-office or at-home) and solutions (deionized distilled water with and without sugar, red wine with and without sugar, coffee with and without sugar) on the effectiveness of in vitro dental bleaching was evaluated. Hydrogen peroxide (HP) 37.5% gel was used for in-office bleaching, 3 applications of 8 min each, 3 sessions with an interval of 7 days. At-home bleaching was performed with 10% Carbamide peroxide (CP), 2 h/day, for 30 days. The enamel vestibular surfaces (n = 72) were subjected daily to test solutions for 45 min, washed with distilled water for 5 min and stored in artificial saliva. The enamel color analysis was performed with a spectrophotometer through color variation (ΔE) and luminosity variation (ΔL). Roughness analysis was performed by atomic force microscopy (AFM) and scanning electron microscopy (SEM). Enamel composition was determined by energy dispersive X-ray spectrometry (EDS). The results were submitted to one-way analysis of variance (ANOVA) for ΔE, ΔL and EDS and two-way for AFM. For ΔE and ΔL there was no statistically significant difference. An increase in roughness was observed on the surface when exposed to a sugar-water solution for at-home bleaching and a lower concentration of Ca and P in the deionized water solution with sugar. Solutions containing or not sugar did not influence the bleaching potential, however the presence of sugar in the water solution increased the surface roughness with CP.

An Overview on the Worlds Dead Liest Poison (Palytoxin and its Analogs)

Abstract: Palytoxin is a marine toxin found originally in soft corals Palythoa species of the Pacific Ocean. It is a thermostable, non-protein, coronary vasoconstrictor that leads to death by diminishing the supply of O2 to the Myocardium. Several analogs of PTX or PTLX such as Ostreocin-D, Ovatoxin are found in several dinoflagellates and other marine species such as Crabs (Demania reynaudii) and Smoked Fishes (Decapterus macrosoma) found in same ecological regions. Toxicological studies of PTX showed low lethal dose values in different mammals revealing the acute toxicity due to different routes of exposure. On exposure to PTX, symptoms such as Rhabdomyolysis (high dose), Na+- K+ pump and heart failure &amp; other symptoms including abdominal cramps, vomiting, bradycardia, etc. are seen in Pescatarians. There is no particular antidote for the PTX compounds, but these compounds can be neutralized by the household bleach solution. Activated Carbon absorbed 99.7% of palytoxin in aquarium waters. In this paper, we review the current knowledge on Palytoxin &amp; its analogs. In recent years, many methodologies have been described for the development of new techniques for the detection of palytoxin based on LC-MS/MS and a bio-technique Immunoassay.

Fabrication of semi-transparent Cu(In,Ga)Se2 solar cells aided by Bromine etching

This study introduces a straightforward and reproducible fabrication method to achieve micro-structured semi-transparent Cu(In,Ga)Se2 (CIGSe) solar cells by lithography and wet etch techniques. We fabricated a segmented micro-structured solar cell by selective etching of an opaque CIGSe solar cell with bromine and bleach solutions and obtained an array of micro lines from 200 µm to 1000 µm in width separated by transparent spaces, resulting in an overall semi-transparent structure. The CIGSe solar cell lines exhibit a maximum power conversion efficiency of 12.4 % for 1000 µm width, which reduces to 6.8 % for 200 µm wide lines. The obtained values are among the highest reported in the literature for similarly architected devices. Our results are a promising step towards the implementation of building integrated CIGSe photovoltaics as windows.

Staphylococcus Infection: Relapsing Atopic Dermatitis and Microbial Restoration.

Atopic Dermatitis (AD) skin is susceptible to Staphylococcus aureus (SA) infection, potentially exposing it to a plethora of toxins and virulent determinants, including Panton-Valentine leukocidin (PVL) (α-hemolysin (Hla) and phenol-soluble modulins (PSMs)), and superantigens. Depending on the degree of infection (superficial or invasive), clinical treatments may encompass permanganate (aq) and bleach solutions coupled with intravenous/oral antibiotics such as amoxicillin, vancomycin, doxycycline, clindamycin, daptomycin, telavancin, linezolid, or tigecycline. However, when the skin is significantly traumatized (sheathing of epidermal sections), an SA infection can rapidly ensue, impairing the immune system, and inducing local and systemic AD presentations in susceptible areas. Furthermore, when AD presents systemically, desensitization can be long (years) and intertwined with periods of relapse. In such circumstances, the identification of triggers (stress or infection) and severity of the flare need careful monitoring (preferably in real-time) so that tailored treatments targeting the underlying pathological mechanisms (SA toxins, elevated immunoglobulins, impaired healing) can be modified, permitting rapid resolution of symptoms.