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Summary
Minerals in the soil range from those that easily weather to those that are very resistant to the weathering processes. The minerals used in this study are referred to as “resistates” because of their resistance to natural weathering processes.1 It is also known that there are some resistate minerals that have a tendency to contain uranium and thorium within their crystal structure. These resistates can contain as much as 15-20% of the total uranium and thorium present in the soil.9 Do resistates dissolve in acids, particularly in the HF/HNO3 procedures, if not what can be done to the HF/HNO3 process to dissolve more of the resistate minerals? How would these acid techniques compare to the fusion method used for mineral dissolution? Could the resistate minerals contain considerable amount of uranium and thorium? These were the questions addressed in this research. The comparative data indicate that the use of H2SO4 in the dissolution process resulted in ~25% overall increase in the minerals dissolving therefore resulting in a higher yield of extracted uranium and thorium.
Abstract
In this study, the stepwise isothermal crystallization or thermal fractionation of Ziegler—Natta and metallocene based polyethylenes (ZN-PE and m-PE) with two kinds of branch lengths (ethyl and hexyl) and branch compositions were studied using simultaneous synchrotron small-angle X-ray scattering (SAXS)/wide-angle X-ray diffraction (WAXD) and differential scanning calorimetry (DSC). The crystal long period and the invariant were determined by SAXS, and the variations of crystal unit cell parameters and the degree of crystallinity were determined by WAXD. The arithmetic mean length (Ln), the weightedmean length (Lw) and the broadness index (Lw/Ln) of the studied polyethylenes were previously determined by DSC. Results from these studies were interpreted using the model of branch exclusion, which affects the ability of the chain-reentry into the crystal phase. Multiple SAXS peaks and step-change in crystallinity change (WAXD) were seen during heating, which corresponded well with the crystal thickness distribution induced by stepwise crystallization. The effects of the heterogeneity of the 1-olefin branch length and the distribution on the crystal long period and the invariant as well as the degree of crystallinity were discussed.
Isospora michaelbakeri is one of the Isospora species most commonly found in the wild field, which can cause severe infection and mortality in young sparrows. In this study, we selected I. michaelbakeri (Chung Hsing strain) as a pathogen to orally inoculate russet sparrows ( Passer rutilans ), spotted munia ( Lonchura punctulata ), canary ( Serinus canaria ), Java sparrows ( Padda oryzivora ), chicken ( Gallus domesticus ), ducks ( Anas platyrhynchos ) and BALB/c mice. The results indicated that I. michaelbakeri infected only russet sparrows. Infected sparrows displayed lethargy, muscular weakness and fluffy feathers, followed by rapid death. Liver and spleen enlargement was seen in the infected birds. Schizonts were identified in thin smears from the venous blood, enlarged livers and spleens. Histopathological examination revealed schizonts and merozoites from the liver and spleen of infected russet sparrows, but not from other species experimentally inoculated with I. michaelbakeri in the present study.
Abstract
The value of urinary cytology in the diagnosis of different pathological conditions in renal transplantation is particularly important. Manual microscopic urinalysis is a high-volume procedure that currently requires significant labour.
Objective: To automate the sediment evaluation and to make this more accurate using the Iris Diagnostics Automated Urine Microscopy Analyzer (iQ200). Our goal was to compare the manual and automated microscopic data to apply iQ200 in renal function monitoring.
Method: The iQ200 uses digital imaging and Auto Analyte Recognition software to classify urine constituents into 12 analyte categories and quantitatively report.
Results: We determined cut-off values of urine particles in every category, which correlated well with manual microscopic results. The iQ200 was more sensitive for pathological casts than manual microscopic analysis. iQ200 helped the operator to differentiate between isomorphic and dismorphic erythrocytes and between lymphocytes and granulocytes, too. Every pathological constituent could be recognized, which is very important for early recognition of renal impairment, graft rejection and urinary tract infection.
Conclusions: The iQ200 system automatically classifies 12 particles, significantly reducing the need for additional sample preparation, manual microscopic review achieving a high degree of standardization in urinalysis.
Data on 54 new for China, India, Korea and Russia species of lichen-forming and lichenicolous fungi, including 22 new for science taxa of lichen-forming and lichenicolous fungi, i.e.: Acarospora ulleungdoensis, Amandinea trassii, Aspicilia geumodoensis, Biatora ivanpisutii, Caloplaca patwolseleyae, Catillaria ulleungdoensis, Coenogonium agonimieoides, Gyalidea austrocoreana, G. ropalosporoides, Opegrapha briancoppinsii, O. ulleungdoensis, Phyllopsora loekoesii, Psoroglaena coreana, Psorotichia gyelnikii, Rinodina oxneriana, Scoliciosporum jasonhurii, Staurothele oxneri, Stigmidium coarctatae, Thelocarpon ulleungdoense, Thelopsis loekoesii, Toninia poeltiana, Unguiculariopsis helmutii, and and 7 new species to China (Caloplaca ussuriensis, Megaspora rimisorediata, Rinodina xanthophaea, Rusavskia dasanensis, Xanthoria splendens, Zeroviella coreana, Z. esfahanensis), and 1 new species to India (Zeroviella esfahanensis), and 24 new species to Korea (Agonimia blumii, Arthonia rinodinicola, Buelliella minimula, Dactylospora australis, Endococcus propinguus, Halecania santessonii, Laeviomyces aff. fallaciosus, Lecanora albescens, L. layana, Lecidella scabra, Micarea farinosa, Minutoexcipula aff. mariana, Opegrapha anomaea, O. aff. xerica, Phoma aff. lecanorina, Polycoccum rubellianae, Porina nucula, Pyrenidium actinellum, Rhexophiale rhexoblephara, Rimularia badioatra, Rinodina confragosa, R. milvina, R. occulta, Tremella phaeophysciae), as well as 1 new species to Russia (Verseghya klarae) are provided. Furthermore new for science species of lichenicolous fungus Polycoccum clauderouxii from China is described. Four new combinations, i.e.: Biatora pseudosambuci (Basionym: Lecanora pseudosambuci S. Y. Kondr., L. Lőkös et J.-S. Hur), Buellia pseudosubnexa (Basionym: Hafellia pseudosubnexa S. Y. Kondr., L. Lőkös et J.-S. Hur), Buellia extremoorientalis (Basionym: Hafellia extremorientalis S. Y. Kondr., L. Lőkös et J.-S. Hur), and Sagedia nunatakkorum (Basionym: Lecanora nunatakkorum Poelt) are proposed. Data on conidiomata and conidia for lichenicolous fungus Opegrapha anomea Nyl are for the first time provided.
Eighteen new to science species, i.e.: 13 taxa from South Korea (Astroplaca loekoesiana S. Y. Kondr., E. Farkas, J.-J. Woo et J.-S. Hur, Buellia ulleungdoensis S. Y. Kondr., L. Lőkös et J.-S. Hur, Candelariella hakulinenii S. Y. Kondr., L. Lőkös et J.-S. Hur, Flavoplaca laszloana S. Y. Kondr. et J.-S. Hur, Lichenostigma epiporpidiae S. Y. Kondr., L. Lőkös et J.-S. Hur, Mikhtomia geumohdoensis S. Y. Kondr., Liu D. et J.-S. Hur, Orientophila dodongensis S. Y. Kondr., L. Lőkös et J.-S. Hur, Physcia orientostellaris S. Y. Kondr., L. Lőkös et J.-S. Hur, Placynthiella hurii S. Y. Kondr. et L. Lőkös, Protoparmeliopsis kopachevskae S. Y. Kondr., L. Lőkös et J.-S. Hur, Psoroglaena sunchonensis S. Y. Kondr., L. Lőkös et J.-S. Hur, Rufoplaca kaernefeltiana S. Y. Kondr., L. Lőkös et J.-S. Hur, Vezdaea poeltiana S. Y. Kondr., L. Lőkös, J. Halda et J.-S. Hur), two species from India (Rusavskia indica S. Y. Kondr. et D. K. Upreti, and R. upretii S. Y. Kondr., G. K. Mishra et S. Nayaka), and two species from Atlantic Europe, i.e.: Spain and Portugal (Xanthoria schummii S. Y. Kondr. and X. lapalmaensis F. Schumm et S. Y. Kondr.), as well as a lichenicolous fungus Leptosphaeria Oxneriae Cl. Roux et S. Y. Kondr. from Asia (Russia and India) are described, illustrated and compared with closely related taxa. Forty species of lichen forming and lichenicolous fungi (i.e.: Acarospora cf. rufescens, Agonimia allobata, A. aff. blumii, Anema decipiens, Anisomeridium aff. albisedum, Bacidia laurocerasi, Cercidospora aff. epipolytropa, C. aff. lobothallia, Dictyocatenulata alba, Fuscopannaria dissecta, Lecanora ussuriensis, Lecidella aff. carpatica, Lemmopsis arnoldiana, Leptosphaeria crozalsii, Lichenostigma cf. bolacinae, L. aff. rupicolae, Lichinella stipatula, L. cribellifera, L. iodopulchra, L. aff. myriospora, Melaspilea proximella, Micarea alabastrites, Opegrapha aff. thelotrematis, Orientophila leucerythrella, Pectenia plumbea, Placynthium tantaleum, Porpidia flavicunda, Psorula rufonigra, Pyrenocarpon aff. thelostomum, Pyrenodesmia duplicata, Pyrenopsis aff. haematina, Ramboldia haematites, Rhizoplaca subdiscrepans, Rimularia gibbosa, Rinodina oxydata, Staurothele frustulenta, Stigmidium cf. clauzadei, Strigula australiensis, Thelenella luridella, Vezdaea leprosa) are for the first time recorded for Korea. Additional locality records for South Korea (74 species) and China (3 species) are also given.
Four new combinations, i.e.: Orientophila chejuensis (for Caloplaca chejuensis S. Y. Kondr. et Hur), Orientophila diffluens (for Lecanora diffluens Hue), Orientophila leucerythrella (for Lecanora leucerythrella Nyl.), and Pyrenodesmia duplicata (for Lecanora duplicata Vain.) are also proposed.
Alectinib is a central nervous system-active small molecule anaplastic lymphoma kinase (ALK) inhibitor that is effective in the treatment of patients with ALK positive tumors, including advanced non-small cell lung cancers and lymphomas. A simple, isocratic high-performance liquid chromatography–photo diode array detection (HPLC–PDA) assay for measurement of alectinib in human plasma is described. Alectinib is extracted from the plasma matrix by addition of methanol, followed by centrifugation and acidification with 0.1% formic acid. It elutes with a run time of 4.6 min using a 250 mm × 4.6 mm RP-C18 column with 0.1% aqueous formic acid and methanol (35:65, v/v) and a flow rate of 1 mL/min. Detection was at 339 nm. Linear calibration plots were achieved in the range of 0.1–20 μg/mL for alectinib (r 2 = 0.9996). With limits of detection and quantification of 0.05 and 0.1 μg/mL, respectively, and excellent precision (%CV < 10%), accuracy (bias < ±12%), and recovery (>97%) within the 1–20 μg/mL concentration range, this assay was suitable for measuring pre-dose alectinib concentrations in an adolescent receiving 600-mg doses twice daily.
Abstract
Subsecond 224 Pa (T
1/2 = 0.85 s) was produced via the 209 Bi(18 O,3n)224 Pa reaction at the 88 inch cyclotron at the Lawrence Berkeley National Laboratory. After production it was transported via a gas-jet system to the centrifuge system SISAK 3. Following on-line extraction with trioctylamine/scintillation solutions from 1M lactic acid, 224 Pa was detected applying on-line 
-liquid scintillation counting. Unambiguous identification was achieved using time-correlated --decay chain analysis. This constitutes the first chemical on-line separation and detection of a subsecond -decaying nuclide, 0.85-s 224 Pa with the fast extraction system SISAK 3.
Abstract
On-line isothermal gas phase chromatography was used to study halides of261104 (T1/2=65 s) and262,263105 (T1/2=34 s and 27 s) produced an atom-at-a time via the reactions248Cm(18O, 5n) and249Bk(18O, 5n, 4n), respectively. Using HBr and HCl gas as halogenating agents, we were able to produce volatile bromides and chlorides of the above mentioned elements and study their behavior compared to their lighter homologs in Groups 4 or 5 of the periodic table. Element 104 formed more volatile bromide than its homolog Hf. In contrast, element 105 bromides were found to be less volatile than the bromides of the group 5 elements Nb and Ta. Both 104 and Hf chlorides were observed to be more volatile than their respective bromides.
