53 research outputs found
Modelling the water balance of Lake Victoria (East Africa) – Part 1: Observational analysis
Lake Victoria is the largest lake in Africa and one of the two major sources
of the Nile river. The water level of Lake Victoria is determined by its
water balance, consisting of precipitation on the lake, evaporation from the
lake, inflow from tributary rivers and lake outflow, controlled by two
hydropower dams. Due to a scarcity of in situ observations, previous estimates
of individual water balance terms are characterized by substantial
uncertainties, which means that the water balance is often not closed
independently. In this first part of a two-paper series, we present a water
balance model for Lake Victoria, using state-of-the-art remote sensing
observations, high-resolution reanalysis downscaling and outflow values
recorded at the dam. The uncalibrated computation of the individual water
balance terms yields lake level fluctuations that closely match the levels
retrieved from satellite altimetry. Precipitation is the main cause of
seasonal and interannual lake level fluctuations, and on average causes the
lake level to rise from May to July and to fall from August to December.
Finally, our results indicate that the 2004–2005 drop in lake level can be
about half attributed to a drought in the Lake Victoria Basin and about half
to an enhanced outflow, highlighting the sensitivity of the lake level to
human operations at the outflow dam.</p
Modelling the water balance of Lake Victoria (East Africa) – Part 2: Future projections
Lake Victoria, the second largest freshwater lake in the world, is one of the
major sources of the Nile river. The outlet to the Nile is controlled by two
hydropower dams of which the allowed discharge is dictated by the Agreed
Curve, an equation relating outflow to lake level. Some regional climate
models project a decrease in precipitation and an increase in evaporation
over Lake Victoria, with potential important implications for its water
balance and resulting level. Yet, little is known about the potential
consequences of climate change for the water balance of Lake Victoria. In
this second part of a two-paper series, we feed a new water balance model for
Lake Victoria presented in the first part with climate simulations available
through the COordinated Regional Climate Downscaling
Experiment (CORDEX) Africa
framework. Our results reveal that most regional climate models are not
capable of giving a realistic representation of the water balance of Lake
Victoria and therefore require bias correction. For two emission scenarios
(RCPs 4.5 and 8.5), the decrease in precipitation over the lake and an
increase in evaporation are compensated by an increase in basin precipitation
leading to more inflow. The future lake level projections show that the dam
management scenario and not the emission scenario is the main controlling
factor of the future water level evolution. Moreover, inter-model
uncertainties are larger than emission scenario uncertainties. The comparison
of four idealized future management scenarios pursuing certain policy
objectives (electricity generation, navigation reliability and environmental
conservation) uncovers that the only sustainable management scenario is
mimicking natural lake level fluctuations by regulating outflow according to
the Agreed Curve. The associated outflow encompasses, however, ranges from
14 m3 day−1 (−85 %) to 200 m3 day−1 (+100 %)
within this ensemble, highlighting that future hydropower generation and
downstream water availability may strongly change in the next decades even if
dam management adheres to he Agreed Curve. Our results overall underline that
managing the dam according to the Agreed Curve is a key prerequisite for
sustainable future lake levels, but that under this management scenario,
climate change might potentially induce profound changes in lake level and
outflow volume.</p
Pseudomonas aeruginosa displays an epidemic population structure.
peer reviewedBacteria can have population structures ranging from the fully sexual to the highly clonal. Despite numerous studies, the population structure of Pseudomonas aeruginosa is still somewhat contentious. We used a polyphasic approach in order to shed new light on this issue. A data set consisting of three outer membrane (lipo)protein gene sequences (oprI, oprL and oprD), a DNA-based fingerprint (amplified fragment length polymorphism), serotype and pyoverdine type of 73 P. aeruginosa clinical and environmental isolates, collected across the world, was analysed using biological data analysis software. We observed a clear mosaicism in the results, non-congruence between results of different typing methods and a microscale mosaic structure in the oprD gene. Hence, in this network, we also observed some clonal complexes characterized by an almost identical data set. The most recent clones exhibited serotypes O1, 6, 11 and 12. No obvious correlation was observed between these dominant clones and habitat or, with the exception of some recent clones, geographical origin. Our results are consistent with, and even clarify, some seemingly contradictory results in earlier epidemiological studies. Therefore, we suggest an epidemic population structure for P. aeruginosa, comparable with that of Neisseria meningitidis, a superficially clonal structure with frequent recombinations, in which occasionally highly successful epidemic clones arise
Evaluation of a microbiological screening and acceptance procedure for cryopreserved skin allografts based on 14 day cultures
Viable donor skin is still considered the gold standard for the temporary covering of burns. Since 1985, the Brussels military skin bank supplies cryopreserved viable cadaveric skin for therapeutic use. Unfortunately, viable skin can not be sterilised, which increases the risk of disease transmission. On the other hand, every effort should be made to ensure that the largest possible part of the donated skin is processed into high-performance grafts. Cryopreserved skin allografts that fail bacterial or fungal screening are reworked into ‘sterile’ non-viable glycerolised skin allografts. The transposition of the European Human Cell and Tissue Directives into Belgian Law has prompted us to install a pragmatic microbiological screening and acceptance procedure, which is based on 14 day enrichment broth cultures of finished product samples and treats the complex issues of ‘acceptable bioburden’ and ‘absence of objectionable organisms’. In this paper we evaluate this procedure applied on 148 skin donations. An incubation time of 14 days allowed for the detection of an additional 16.9% (25/148) of contaminated skin compared to our classic 3 day incubation protocol and consequently increased the share of non-viable glycerolised skin with 8.4%. Importantly, 24% of these slow-growing microorganisms were considered to be potentially pathogenic. In addition, we raise the issue of ‘representative sampling’ of heterogeneously contaminated skin. In summary, we feel that our present microbiological testing and acceptance procedure assures adequate patient safety and skin availability. The question remains, however, whether the supposed increased safety of our skin grafts outweighs the reduced overall clinical performance and the increase in work load and costs
Zilucoplan in immune-mediated necrotising myopathy: a phase 2, randomised, double-blind, placebo-controlled, multicentre trial
BACKGROUND:
Immune-mediated necrotising myopathy is an autoimmune myopathy characterised by proximal muscle weakness, high creatine kinase concentrations, and autoantibodies recognising 3-hydroxy-3-methylglutaryl-coenzyme A reductase (HMGCR) or the signal recognition particle (SRP). No approved therapies exist for people with immune-mediated necrotising myopathy. Previous studies have suggested that complement activation might be pathogenic in immune-mediated necrotising myopathy; therefore, zilucoplan, a complement C5 (C5) inhibitor, could be a potential therapy. We aimed to evaluate the efficacy, safety, and tolerability of zilucoplan in adult participants with anti-HMGCR or anti-SRP autoantibody-positive immune-mediated necrotising myopathy.
METHODS:
IMNM-01 was a phase 2, multicentre, randomised, double-blind, placebo-controlled study done at 15 hospital sites across the USA, the UK, France, and the Netherlands. Participants aged 18–74 years were eligible for inclusion if they had a clinically confirmed diagnosis of immune-mediated necrotising myopathy, positive serology for anti-HMGCR or anti-SRP autoantibodies, clinical evidence of weakness, serum total creatine kinase concentration of more than 1000 U/L at screening, and no change in glucocorticoids or other immunosuppressive therapies for 30 days before baseline or expected during the first 8 weeks of the study. Participants were randomly assigned (1:1) to receive daily subcutaneous zilucoplan (0·3 mg/kg) or placebo for 8 weeks by use of a computerised randomisation algorithm; with optional enrolment in the study open-label extension. Randomisation was stratified by autoantibody status. Participants and study staff were masked to treatment group assignment. Primary efficacy endpoint (in the intent-to-treat population, defined as all participants who were randomly assigned to a treatment group) was percent change from baseline to week 8 in creatine kinase concentrations. Safety analyses were performed on the safety population (participants who received at least one dose of study drug during the main study, irrespective of whether they continued to the extension period—study participants were analysed on the basis of the treatment received). This study is registered with ClinicalTrials.gov, NCT04025632.
FINDINGS:
Between Nov 7, 2019, and Jan 7, 2021, we randomly assigned 27 participants (13 female and 14 male) to receive zilucoplan (n=12) or placebo (n=15). All 27 participants completed the 8-week main study. At week 8 there were no significant differences between treatment groups in median percent change of creatine kinase concentrations versus baseline (–15·1% [IQR –31·1 to 3·2] in the zilucoplan group vs –16·3% [–43·8 to 5·9] in the placebo group; p=0·46) and no clinically relevant improvement over time within the treatment group despite target engagement based on mode of action. There were no unexpected adverse safety or tolerability findings. Treatment-emergent adverse events were reported in nine (75%) of 12 participants in the zilucoplan group, and in 13 (87%) of 15 participants in the placebo group, and serious treatment-emergent adverse events were reported in zero participants in the zilucoplan group and three (20%) participants in the placebo group. The most frequent treatment-emergent adverse events were headache (four [33%] participants in the zilucoplan group and four [27%] participants in the placebo group) and nausea (three [25%] participants in the zilucoplan group and three [20%] participants in the placebo group).
INTERPRETATION:
C5 inhibition does not appear to be an efficacious treatment modality for people with immune-mediated necrotising myopathy. Rather than being the primary driver for disease activity, complement activation might be secondary to muscle injury.
FUNDING:
Ra Pharmaceuticals (now part of UCB Pharma)
Feeder layer- and animal product-free culture of neonatal foreskin keratinocytes: improved performance, usability, quality and safety
Since 1987, keratinocytes have been cultured at the Queen Astrid Military Hospital. These keratinocytes have been used routinely as auto and allografts on more than 1,000 patients, primarily to accelerate the healing of burns and chronic wounds. Initially the method of Rheinwald and Green was used to prepare cultured epithelial autografts, starting from skin samples from burn patients and using animal-derived feeder layers and media containing animal-derived products. More recently we systematically optimised our production system to accommodate scientific advances and legal changes. An important step was the removal of the mouse fibroblast feeder layer from the cell culture system. Thereafter we introduced neonatal foreskin keratinocytes (NFK) as source of cultured epithelial allografts, which significantly increased the consistency and the reliability of our cell production. NFK master and working cell banks were established, which were extensively screened and characterised. An ISO 9001 certified Quality Management System (QMS) governs all aspects of testing, validation and traceability. Finally, as far as possible, animal components were systematically removed from the cell culture environment. Today, quality controlled allograft production batches are routine and, due to efficient cryopreservation, stocks are created for off-the-shelf use. These optimisations have significantly increased the performance, usability, quality and safety of our allografts. This paper describes, in detail, our current cryopreserved allograft production process
Heat stored in the Earth system 1960–2020: where does the energy go?
The Earth climate system is out of energy balance, and heat has
accumulated continuously over the past decades, warming the ocean, the land,
the cryosphere, and the atmosphere. According to the Sixth Assessment Report
by Working Group I of the Intergovernmental Panel on Climate Change,
this planetary warming over multiple decades is human-driven and results in
unprecedented and committed changes to the Earth system, with adverse
impacts for ecosystems and human systems. The Earth heat inventory provides
a measure of the Earth energy imbalance (EEI) and allows for quantifying
how much heat has accumulated in the Earth system, as well as where the heat is
stored. Here we show that the Earth system has continued to accumulate
heat, with 381±61 ZJ accumulated from 1971 to 2020. This is equivalent to a
heating rate (i.e., the EEI) of 0.48±0.1 W m−2. The majority,
about 89 %, of this heat is stored in the ocean, followed by about 6 %
on land, 1 % in the atmosphere, and about 4 % available for melting
the cryosphere. Over the most recent period (2006–2020), the EEI amounts to
0.76±0.2 W m−2. The Earth energy imbalance is the most
fundamental global climate indicator that the scientific community and the
public can use as the measure of how well the world is doing in the task of
bringing anthropogenic climate change under control. Moreover, this
indicator is highly complementary to other established ones like global mean
surface temperature as it represents a robust measure of the rate of climate
change and its future commitment. We call for an implementation of the
Earth energy imbalance into the Paris Agreement's Global Stocktake based on
best available science. The Earth heat inventory in this study, updated from
von Schuckmann et al. (2020), is underpinned by worldwide multidisciplinary
collaboration and demonstrates the critical importance of concerted
international efforts for climate change monitoring and community-based
recommendations and we also call for urgently needed actions for enabling
continuity, archiving, rescuing, and calibrating efforts to assure improved
and long-term monitoring capacity of the global climate observing system. The data for the Earth heat inventory are publicly available, and more details are provided in Table 4.</p
Scenario setup and forcing data for impact model evaluation and impact attribution within the third round of the Inter-Sectoral Model Intercomparison Project (ISIMIP3a)
This paper describes the rationale and the protocol of the first component of the third simulation round of the Inter-Sectoral Impact Model Intercomparison Project (ISIMIP3a, http://www.isimip.org, last access: 2 November 2023) and the associated set of climate-related and direct human forcing data (CRF and DHF, respectively). The observation-based climate-related forcings for the first time include high-resolution observational climate forcings derived by orographic downscaling, monthly to hourly coastal water levels, and wind fields associated with historical tropical cyclones. The DHFs include land use patterns, population densities, information about water and agricultural management, and fishing intensities. The ISIMIP3a impact model simulations driven by these observation-based climate-related and direct human forcings are designed to test to what degree the impact models can explain observed changes in natural and human systems. In a second set of ISIMIP3a experiments the participating impact models are forced by the same DHFs but a counterfactual set of atmospheric forcings and coastal water levels where observed trends have been removed. These experiments are designed to allow for the attribution of observed changes in natural, human, and managed systems to climate change, rising CH4 and CO2 concentrations, and sea level rise according to the definition of the Working Group II contribution to the IPCC AR6.</p
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Global heat uptake by inland waters
Heat uptake is a key variable for understanding the Earth system response to greenhouse gas forcing. Despite the importance of this heat budget, heat uptake by inland waters has so far not been quantified. Here we use a unique combination of global-scale lake models, global hydrological models and Earth system models to quantify global heat uptake by natural lakes, reservoirs, and rivers. The total net heat uptake by inland waters amounts to 2.6 ± 3.2 ×1020 J over the period 1900–2020, corresponding to 3.6% of the energy stored on land. The overall uptake is dominated by natural lakes (111.7%), followed by reservoir warming (2.3%). Rivers contribute negatively (-14%) due to a decreasing water volume. The thermal energy of water stored in artificial reservoirs exceeds inland water heat uptake by a factor ∼10.4. This first quantification underlines that the heat uptake by inland waters is relatively small, but non-negligible
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