Abstract. Coban Rondo waterfall is threated to have been polluted due to the tourism activity. Analysis of the water quality is essential to provide the basis for judging the suitability of water for its designated uses and improving its conditions. This study aims to analyze the water physical and chemical parameters of Coban Rondo waterfall in Pujon, Malang Indonesia. Three locations including upstream, waterfall, and downstream were the sources of the water samples taken during the rainy season. The study analyzes 12 water quality parameters consisting of 5 physical parameters and 7 chemical parameters. Using ANOVA, cluster analyses, and Biplot to analyze the water quality, the research results indicated that water and air temperatures were high in the upstream. The value of pH from 6.9 to 7.4, DO from 8 to 11 mg/L, conductivity from 0.106-0.112dS/m, turbidity 3.3 NTU to 7.6 NTU, water debit4 x 105 L/s and total phosphate from 0.5to 0.07 mg/L were higher in the downstream area, while the concentration of nitrate from 5 to 30 mg/L, orthophosphate 1.0 to 1.4 mg/L, COD from 14 to 22 mg/Land BOD 10.8 to 15.6mg/L was highest in the upstream. It indicates that the human activity in Coban Rondo has affected the water quality. Based on Indonesia government regulation No. 82/2001, the water in Coban Rondo was still suitable for irrigation and tourism (Class II), except BOD level.

Keyword: Coban Rondo waterfall, physical chemical parameters, water quality.

Abstract

Purpose In this literature review, functional outcomes such as Disability of Arm, Shoulder and Hand (DASH) score and the visual analog scale (VAS) of pain along with clinical outcomes such as range of movement and grip strength of treated distal radius fractures (DRF) accompanied with ulnar styloid fractures (USF) will be compared with those with isolated DRF. Materials and Methods We analyzed articles from MEDLINE, Embase, and CINAHL that met our predetermined inclusion and exclusion criteria as per the Preferred Reporting Items for Systematic Reviews and Meta-analysis statements. This resulted in the identification of 464 articles with 18 potentially eligible studies of which 6 were included at the full-text screening stage. The primary outcomes were wrist pain, range of motion, functional outcome and satisfaction, such as VAS, and the DASH questionnaire along with radiological assessment and incidence of complications. Results These studies involved 796 participants with DRF and 806 wrists with DRF; 444 (55%) of DRF had an associated USF. Three studies did not report any statistically significant difference in DASH scores between the DRF patients with or without USF. Two studies reported worse DASH scores in the group with associated USF. Wrist pain was reported to be statistically significantly worse in patients with associated USF in two studies. Grip strength did not exhibit a statistically significant difference in any groups in four studies. On assessing the range of motion of the wrist and forearm, only one study reported a statistically significant difference in flexion at 2 years follow-up, with less flexion in patients with USF. Conclusion This review suggests that there is no significant correlation between a USF and the functional and clinical outcomes of DRF treatment, albeit wrist pain and less flexion were reported in some studies to be associated with USF. There is a need for more robust evidence from large randomized controlled trials to specifically look at the effects of fixation versus nonfixation of USF on DRF, or large prospective cohort studies assessing DRF with and without USF, with a minimum of 12 months follow-up. Level of Evidence Level II-therapeutic.

The in vitro cell culture environment can impact on cell biochemistry and cell cycle. The manifestation of such substrate-induced changes in cell cycle in the Raman microspectroscopic profiles of cell cultures is investigated at the level of nucleolus, nucleus and cytoplasm. HeLa immortalised human cervical cells and HaCaT dermal cells were cultured on three different substrates, conventional polystyrene cell culture dishes, CaF2 slides as a commonly used Raman substrate, and glass slides coated with Collagen Rat Tail, as a mimic of the extra cellular matrix (ECM) environment. A cell cycle study, based on percentage DNA content, as determined using Propidium Iodide staining and monitored by flow cytometry, was performed on cells of both types, grown on the different substrates, confirming that the in vitro cell culture environment impacts significantly on the cell cycle. Live cell in vitro Raman spectroscopic analysis of cells on the 2D CaF2 and 3D Collagen substrates was performed and data was analysed using principal components analysis (PCA). The spectroscopic analysis revealed differences in profiles which reflect the differences in cell cycle for both in vitro culture environments. In particular, the Raman spectra of cells 2 grown on CaF2 show indicators of cell stress, which are also associated with cell cycle arrest at the G0/G1 phase. This work contributes to the field of Raman spectroscopic analysis by providing a fresh look at the significance of the effect of in vitro culture environment to cell cycle and the sensitivity of Raman spectroscopy to such differences in cell metabolism. 

Abstract. The growth of lampenflora detracts the natural beauty of cave walls, and threatens their archaeological value.

This is a real problem in Malaysian caves, therefore, an attempt should be made to eliminate these unwanted microorganisms. Ultraviolet light destroys harmful microbes such as bacteria, yeast. molds, viruses and algae, and ultraviolet radiation is less toxic to cave dwellers such as birds, reptiles and visitors. So ultraviolet radiation can be a way to control microorganisms or reduce their numbers. In this study. we studied the effect of ultraviolet radiation on microorganisms isolated from selected Malaysian caves to control and eliminate them AlterS minutes exposure, 254mm UV-C effectively eliminated colonies of Pseudomonas aerginosa and Stenotrophomonas sp. But P. guilliermondi and

R. dairenensis were eliminated to the zero after 30 mivutes of treatment, but C. Liquefaciens needed 60 minutes to be treated. Synechochococcus sp and Micractinium sp. fell to zero after exposure to 240 of UV-C