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result(s) for
"Blunk, Jan"
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Early warning of complex climate risk with integrated artificial intelligence
by
Frank, Dorothea
,
Rahaman, Nasim
,
Camps-Valls, Gustau
in
704/172/4081
,
704/4111
,
Artificial intelligence
2025
As climate change accelerates, human societies face growing exposure to disasters and stress, highlighting the urgent need for effective early warning systems (EWS). These systems monitor, assess, and communicate risks to support resilience and sustainable development, but challenges remain in hazard forecasting, risk communication, and decision-making. This perspective explores the transformative potential of integrated Artificial Intelligence (AI) modeling. We highlight the role of AI in developing multi-hazard EWSs that integrate Meteorological and Geospatial foundation models (FMs) for impact prediction. A user-centric approach with intuitive interfaces and community feedback is emphasized to improve crisis management. To address climate risk complexity, we advocate for causal AI models to avoid spurious predictions and stress the need for responsible AI practices. We highlight the FATES (Fairness, Accountability, Transparency, Ethics, and Sustainability) principles as essential for equitable and trustworthy AI-based Early Warning Systems for all. We further advocate for decadal EWSs, leveraging climate ensembles and generative methods to enable long-term, spatially resolved forecasts for proactive climate adaptation.
In the era of climate change, human societies face growing exposure to disasters and complex climate risks. This perspective explores the transformative potential of integrated Artificial Intelligence in developing multi-hazard Early Warning Systems for all.
Journal Article
CausalRivers -- Scaling up benchmarking of causal discovery for real-world time-series
2025
Causal discovery, or identifying causal relationships from observational data, is a notoriously challenging task, with numerous methods proposed to tackle it. Despite this, in-the-wild evaluation of these methods is still lacking, as works frequently rely on synthetic data evaluation and sparse real-world examples under critical theoretical assumptions. Real-world causal structures, however, are often complex, making it hard to decide on a proper causal discovery strategy. To bridge this gap, we introduce CausalRivers, the largest in-the-wild causal discovery benchmarking kit for time-series data to date. CausalRivers features an extensive dataset on river discharge that covers the eastern German territory (666 measurement stations) and the state of Bavaria (494 measurement stations). It spans the years 2019 to 2023 with a 15-minute temporal resolution. Further, we provide additional data from a flood around the Elbe River, as an event with a pronounced distributional shift. Leveraging multiple sources of information and time-series meta-data, we constructed two distinct causal ground truth graphs (Bavaria and eastern Germany). These graphs can be sampled to generate thousands of subgraphs to benchmark causal discovery across diverse and challenging settings. To demonstrate the utility of CausalRivers, we evaluate several causal discovery approaches through a set of experiments to identify areas for improvement. CausalRivers has the potential to facilitate robust evaluations and comparisons of causal discovery methods. Besides this primary purpose, we also expect that this dataset will be relevant for connected areas of research, such as time-series forecasting and anomaly detection. Based on this, we hope to push benchmark-driven method development that fosters advanced techniques for causal discovery, as is the case for many other areas of machine learning.
Endothelial cell heterogeneity and microglia regulons revealed by a pig cell landscape at single-cell level
2022
Pigs are valuable large animal models for biomedical and genetic research, but insights into the tissue- and cell-type-specific transcriptome and heterogeneity remain limited. By leveraging single-cell RNA sequencing, we generate a multiple-organ single-cell transcriptomic map containing over 200,000 pig cells from 20 tissues/organs. We comprehensively characterize the heterogeneity of cells in tissues and identify 234 cell clusters, representing 58 major cell types. In-depth integrative analysis of endothelial cells reveals a high degree of heterogeneity. We identify several functionally distinct endothelial cell phenotypes, including an endothelial to mesenchymal transition subtype in adipose tissues. Intercellular communication analysis predicts tissue- and cell type-specific crosstalk between endothelial cells and other cell types through the
VEGF
,
PDGF
,
TGF-β
, and
BMP
pathways. Regulon analysis of single-cell transcriptome of microglia in pig and 12 other species further identifies
MEF2C
as an evolutionally conserved regulon in the microglia. Our work describes the landscape of single-cell transcriptomes within diverse pig organs and identifies the heterogeneity of endothelial cells and evolutionally conserved regulon in microglia.
Pigs are important large animal models for biomedical research. Here, the authors construct a single-cell landscape of pig tissues, unravelling the phenotypic heterogeneity of blood endothelial cells in adipose tissues and the evolutionally conserved regulons of microglia in brains.
Journal Article
Genomic imprinting analyses identify maternal effects as a cause of phenotypic variability in type 1 diabetes and rheumatoid arthritis
2020
Imprinted genes, giving rise to parent-of-origin effects (POEs), have been hypothesised to affect type 1 diabetes (T1D) and rheumatoid arthritis (RA). However, maternal effects may also play a role. By using a mixed model that is able to simultaneously consider all kinds of POEs, the importance of POEs for the development of T1D and RA was investigated in a variance components analysis. The analysis was based on Swedish population-scale pedigree data. With
P
= 0.18 (T1D) and
P
= 0.26 (RA) imprinting variances were not significant. Explaining up to 19.00% (± 2.00%) and 15.00% (± 6.00%) of the phenotypic variance, the maternal environmental variance was significant for T1D (
P
= 1.60 × 10
−24
) and for RA (
P
= 0.02). For the first time, the existence of maternal genetic effects on RA was indicated, contributing up to 16.00% (± 3.00%) of the total variance. Environmental factors such as the social economic index, the number of offspring, birth year as well as their interactions with sex showed large effects.
Journal Article