30 research outputs found

    Lokal overvannshĂ„ndtering – regnbed Bolstadhagen, Drammen

    Get PDF
    Norges miljþ‐ og biovitenskapelige universitet (NMBU) har i samarbeid med Drammen kommune gjennomfĂžrt et forskningsprosjekt for Ă„ vurdere hvordan Bolstadhagen regnbed (som bestĂ„r av 4 deler i serie, bed 1‐4) fungerer i driftsfasen. I dette inngĂ„r mĂ„ling av infiltrasjonsevne, kapasitet (vannbalanse), vinterforhold, vannkvalitet og plantenes egnethet. Jordsammensetningen som er lik i alle bedene har en kornfordeling og organisk innhold som oppgitt av produsenten (Lindum). Gjennomsnittlig infiltrasjonsevne i regnbedet var i 2017 ca 9 cm/t som er litt i underkant av anbefalt grense pĂ„ 10 cm/t. Gjentak av mĂ„lingene i 2020 ga en gjennomsnittlig infiltrasjonsevne (kun mĂ„lt i de to nederste bedene, 3 og 4) pĂ„ 22 cm/t i 2020, denne Ăžkningen samsvarer med mĂ„linger i forskningsregnbedet pĂ„ NMBU. I de to Ăžverste bedene ble det observert stĂ„ende vann fra vinteren 2019 frem til hĂžsten 2020. Dette skyldes mest sannsynlig Ăžkt partikkel transport pĂ„ grunn av manglende tĂžmming av sandfang. Dette har sannsynligvis ogsĂ„ inkludert finmateriale som har sedimentert i dammene som dannes i bed 1 og 2 og tettet porerommene. Basert pĂ„ vannfĂžringsmĂ„linger i kum som fordeler vann inn pĂ„ regnbedet, i utlĂžpskum og i overlĂžpskum ettervinteren 2018, var anlegget overdimensjonert i forhold til vannmengdene som ble tilfĂžrt. Mer vann ble derfor tilkoblet i 23.04.18, dette Ăžkte vannfĂžringen inn pĂ„ anlegget og ga vann til overlĂžp (dette skjedde ved enkelte nedbĂžrhendelser >10‐20mm/dĂžgn). Vannmengdene var en stĂžrrelsesorden lavere enn det som ble mĂ„lt i innlĂžpskummen. Forutsatt at man bedrer tĂžmmerutinene i sandfang fĂžr innlĂžpet til regnbedet, og utbedrer infiltrasjonsevnen i bed 1 og 2, kan man fortsatt optimalisere mengder vann til anlegget og om mulig redusere vann til overlĂžp ettersom det fortsatt er ubrukt kapasitet pĂ„ regnbed/Q‐bic magasin. Basert pĂ„ vannanalyser fra inn‐ og utlĂžpskummene til Bolstadhagen, er vannet lite pĂ„virket av veisalt (maks 26 mg Cl/l, sammenliknet med 380 mg Cl/l i et veinĂŠrt regnbed i Drammen kommune: BjĂžrnstjerne BjĂžrnsonsgate). Generelt er det lite forurensinger i vannet som infiltrerer i regnbedet, og det er heller ikke observert utlekking av nĂŠringsstoffer fra jordfilteret som kan oppstĂ„ i konstruerte jordfilter pga innblanding med kompost. Generelt kan det ta noen Ă„r fĂžr nyplantinger etablerer seg. Fra mai 2018 ble det ekstremt varmt og tĂžrt og dette varte til begynnelsen av august, dette gav svĂŠrt dĂ„rlig plantevekstvekst utover sommeren. Det var tydelig forskjell mellom arter i lĂžpet av sesongen. Til tross for vanning gjennom sommeren 2018 var det fĂžrst etter stĂžrre nedbĂžrmengder i august at plantene kom i god vekst. Etter fĂžrste leveĂ„r (2017/18) var det ingen av plantene som hadde gĂ„tt ut, bortsett fra de som hadde fĂ„tt trĂ„kkskader. Salttoleranse kunne ikke vurderes da det var lite salt i vann som infiltrerte regnbedet denne vinteren. Etter vinteren 2019/20 hadde mange planter i bed 1 og 2 fĂ„tt varige skader pĂ„ grunn av langvarig stĂ„ende vann. BĂ„de planter og infiltrasjonsevne ble pĂ„virket av vinterforhold og frost i bakken. Vinteren 2017/18 var snĂžrik med 89‐207mm vannekvivalenter ved slutten av snĂžsesongen. Et islag ble observert i bunnen av flere av regnbedene allerede i januar, og til tross for at snĂžen hadde smeltet i begynnelsen av april var ikke islaget borte fĂžr i slutten av april i regnbedene. Dette redusert infiltrasjonsevnen bĂ„de gjennom vinteren og i snĂžsmeltingen. Dette kan gi problemer med oksygentilgjengelighet for planter, det utsetter ogsĂ„ vekstsesongen. Etter vinteren 2017/18 ble det installert jordtemperatur og fuktsensorer i regnbedet, som det er viktig Ă„ fĂžlge opp slik at man fĂ„r observasjoner som kompletterer overflate observasjonene gjennom flere vintre. Attraksjonsverdi er ikke vurdert generelt, men i forhold til hvordan plantene fremsto vĂ„r og sommer 2018, hadde bĂ„de isbrann og tĂžrke virket negativt inn pĂ„ plantene. Etter godt med nedbĂžr i august 2018 var plantene frodige og hadde hĂžy attraksjonsverdi. Regnbedet fremstod da som et positivt element i skolegĂ„rden og for turgĂ„ere i omrĂ„det. PĂ„ grunn av nevnte problemer med stĂ„ende vann i bed 1 og 2 opptrer regnbedet som noe redusert hĂžsten 2020 sammenliknet med tilstanden hĂžsten 2018.The Norwegian University of Life Sciences (NMBU) has in collaboration with Drammen municipality carried out a study of the functionality of Bolstadhagen raingarden (consisting of 4 sections in series, 1‐4) during the operational phase. This includes measuring infiltration, capacity (water balance), winter conditions, water quality and the suitability of the plants. The soil composition has a grain distribution and organic content as stated by the producer (Lindum). The average infiltration capacity in the raingarden in 2017 was 9 cm/h, which is slightly lower than the recommendation of 10 cm/h, but in 2020 the infiltration capacity had increased to 22 cm/h (could only be measured in the two lower sections, 3 and 4). In the two upper sections (1 and 2) standing water was observed from winter 2019 until autumn 2020, most likely because the sand trap upstream was not emptied as prescribed (causing input of fine sediments and sedimentation in the ponded water). Based on water flow measurements in manholes that distribute water into and out of the rain garden and via the overflow (by‐passing the rain garden), the initial capacity of the rain garden appears to be over dimensioned. Surface water pipes from a larger area was connected to the raingarden 23.04.18, this increased the discharge into the raingarden and caused water to overflow (this occurred during some precipitation events > 10‐20mm/day). The water volumes out of the raingarden during these events were an order of magnitude lower than what was measured in the inlet manhole. Assuming improved emptying routines of the sand trap before the inlet to the raingarden, and improved infiltration in sections 1 and 2, discharge rates could still be optimized further as there is unused storage capacity in the raingarden plus the storage volume below the raingarden (Q‐bic reservoirs). Based on water analyses, there is little contaminants in the incoming water to the raingarden, and no leakage of nutrients in the water drained from the raingarden filter material (soil). No or low salt concentrations were observed in snow and meltwater that infiltrated the raingarden. In general, it may take a few years before new plantings (2017) are established. From May 2018 it became extremely hot and dry and this lasted until the beginning of August, this gave poor plant growth over the summer. There was a clear difference between species. Despite irrigation during the summer, improvements in plant growth could only be observed after heavy rainfall in August. After the first year (2018) since the establishment of the raingarden, none of the plants had died, except for those that had been exposed to trampling. Salt tolerance could not be evaluated as there was little salt in the water that infiltrated the raingarden that winter. The winter of 2019/20 gave permanent damage to many of the plants in section 1 and 2 because of prolonged standing water. The winter of 2017/18 was snowy with 89‐207mm water equivalents at the end of the snow season. Both plants and infiltration were affected by winter conditions and frost in the ground. An ice layer was observed at the bottom of several of the raingarden sections already in January, and despite snow having melted by early April, the ice layer had not melted by the end of April in the raingarden. The reduced infiltration capacity both during winter and snowmelt can cause problems with oxygen availability for plants, it also postpones the growing season. After the winter of 2017/18, soil temperature and moisture sensors were installed in the raingarden (section 1). This provides useful seasonal information which complements surface observations. Attraction value was not assessed in general but considering how the plants appeared in spring and summer of 2018, both ice conditions of the preceding winter followed by summer drought caused a negative effect on the plants. After plentiful rainfall in August 2018, the plants were lush with a high attraction value. The raingarden appeared as a positive element in the schoolyard and by passers in the area. Due to the mentioned problems with standing water in sections 1 and 2, the raingarden appeared to be somewhat reduced in the autumn of 2020 compared to the condition in the autumn of 2018

    Disease-associated mutations in a bifunctional aminoacyl-tRNA synthetase gene elicit the integrated stress response

    Get PDF
    Aminoacyl-tRNA synthetases (ARSs) catalyze the charging of specific amino acids onto cognate tRNAs, an essential process for protein synthesis. Mutations in ARSs are frequently associated with a variety of human diseases. The human EPRS1 gene encodes a bifunctional glutamyl-prolyl-tRNA synthetase (EPRS) with two catalytic cores and appended domains that contribute to nontranslational functions. In this study, we report compound heterozygous mutations in EPRS1, which lead to amino acid substitutions P14R and E205G in two patients with diabetes and bone diseases. While neither mutation affects tRNA binding or association of EPRS with the multisynthetase complex, E205G in the glutamyl-tRNA synthetase (ERS) region of EPRS is defective in amino acid activation and tRNAGlu charging. The P14R mutation induces a conformational change and altered tRNA charging kinetics in vitro. We propose that the altered catalytic activity and conformational changes in the EPRS variants sensitize patient cells to stress, triggering an increased integrated stress response (ISR) that diminishes cell viability. Indeed, patient-derived cells expressing the compound heterozygous EPRS show heightened induction of the ISR, suggestive of disruptions in protein homeostasis. These results have important implications for understanding ARS-associated human disease mechanisms and development of new therapeutics

    A Multilaboratory Comparison of Calibration Accuracy and the Performance of External References in Analytical Ultracentrifugation

    Get PDF
    Analytical ultracentrifugation (AUC) is a first principles based method to determine absolute sedimentation coefficients and buoyant molar masses of macromolecules and their complexes, reporting on their size and shape in free solution. The purpose of this multi-laboratory study was to establish the precision and accuracy of basic data dimensions in AUC and validate previously proposed calibration techniques. Three kits of AUC cell assemblies containing radial and temperature calibration tools and a bovine serum albumin (BSA) reference sample were shared among 67 laboratories, generating 129 comprehensive data sets. These allowed for an assessment of many parameters of instrument performance, including accuracy of the reported scan time after the start of centrifugation, the accuracy of the temperature calibration, and the accuracy of the radial magnification. The range of sedimentation coefficients obtained for BSA monomer in different instruments and using different optical systems was from 3.655 S to 4.949 S, with a mean and standard deviation of (4.304 ± 0.188) S (4.4%). After the combined application of correction factors derived from the external calibration references for elapsed time, scan velocity, temperature, and radial magnification, the range of s-values was reduced 7-fold with a mean of 4.325 S and a 6-fold reduced standard deviation of ± 0.030 S (0.7%). In addition, the large data set provided an opportunity to determine the instrument-to-instrument variation of the absolute radial positions reported in the scan files, the precision of photometric or refractometric signal magnitudes, and the precision of the calculated apparent molar mass of BSA monomer and the fraction of BSA dimers. These results highlight the necessity and effectiveness of independent calibration of basic AUC data dimensions for reliable quantitative studies

    A Multilaboratory Comparison of Calibration Accuracy and the Performance of External References in Analytical Ultracentrifugation

    Get PDF
    Analytical ultracentrifugation (AUC) is a first principles based method to determine absolute sedimentation coefficients and buoyant molar masses of macromolecules and their complexes, reporting on their size and shape in free solution. The purpose of this multi-laboratory study was to establish the precision and accuracy of basic data dimensions in AUC and validate previously proposed calibration techniques. Three kits of AUC cell assemblies containing radial and temperature calibration tools and a bovine serum albumin (BSA) reference sample were shared among 67 laboratories, generating 129 comprehensive data sets. These allowed for an assessment of many parameters of instrument performance, including accuracy of the reported scan time after the start of centrifugation, the accuracy of the temperature calibration, and the accuracy of the radial magnification. The range of sedimentation coefficients obtained for BSA monomer in different instruments and using different optical systems was from 3.655 S to 4.949 S, with a mean and standard deviation of (4.304 ± 0.188) S (4.4%). After the combined application of correction factors derived from the external calibration references for elapsed time, scan velocity, temperature, and radial magnification, the range of s-values was reduced 7-fold with a mean of 4.325 S and a 6-fold reduced standard deviation of ± 0.030 S (0.7%). In addition, the large data set provided an opportunity to determine the instrument-to-instrument variation of the absolute radial positions reported in the scan files, the precision of photometric or refractometric signal magnitudes, and the precision of the calculated apparent molar mass of BSA monomer and the fraction of BSA dimers. These results highlight the necessity and effectiveness of independent calibration of basic AUC data dimensions for reliable quantitative studies

    A multilaboratory comparison of calibration accuracy and the performance of external references in analytical ultracentrifugation.

    Get PDF
    Analytical ultracentrifugation (AUC) is a first principles based method to determine absolute sedimentation coefficients and buoyant molar masses of macromolecules and their complexes, reporting on their size and shape in free solution. The purpose of this multi-laboratory study was to establish the precision and accuracy of basic data dimensions in AUC and validate previously proposed calibration techniques. Three kits of AUC cell assemblies containing radial and temperature calibration tools and a bovine serum albumin (BSA) reference sample were shared among 67 laboratories, generating 129 comprehensive data sets. These allowed for an assessment of many parameters of instrument performance, including accuracy of the reported scan time after the start of centrifugation, the accuracy of the temperature calibration, and the accuracy of the radial magnification. The range of sedimentation coefficients obtained for BSA monomer in different instruments and using different optical systems was from 3.655 S to 4.949 S, with a mean and standard deviation of (4.304 ± 0.188) S (4.4%). After the combined application of correction factors derived from the external calibration references for elapsed time, scan velocity, temperature, and radial magnification, the range of s-values was reduced 7-fold with a mean of 4.325 S and a 6-fold reduced standard deviation of ± 0.030 S (0.7%). In addition, the large data set provided an opportunity to determine the instrument-to-instrument variation of the absolute radial positions reported in the scan files, the precision of photometric or refractometric signal magnitudes, and the precision of the calculated apparent molar mass of BSA monomer and the fraction of BSA dimers. These results highlight the necessity and effectiveness of independent calibration of basic AUC data dimensions for reliable quantitative studies

    A Unified Kinetic Mechanism Applicable to Multiple DNA Polymerases

    No full text
    corecore