
World's richest 10% caused two-thirds of global warming: study
The world's wealthiest 10 percent of individuals are responsible for two-thirds of global warming since 1990, researchers said on Wednesday.
How the rich consume and invest has substantially increased the risk of deadly heatwaves and drought, they reported in the first study to quantify the impact of concentrated private wealth on extreme climate events.
"We link the carbon footprints of the wealthiest individuals directly to real-world climate impacts," lead author Sarah Schoengart, a scientist at ETH Zurich, told AFP.
"It's a shift from carbon accounting toward climate accountability."
Compared to the global average, for example, the richest one percent contributed 26 times more to once-a-century heatwaves, and 17 times more to droughts in the Amazon, according to the findings, published in Nature Climate Change.
Emissions from the wealthiest 10 percent in China and the United States - which together account for nearly half of global carbon pollution - each led to a two-to-threefold rise in heat extremes.
Burning fossil fuels and deforestation have heated Earth's average surface by 1.3 degrees Celsius, mostly during the last 30 years.
Schoengart and colleagues combined economic data and climate simulations to trace emissions from different global income groups and assess their impact on specific types of climate-enhance extreme weather.
The researchers also emphasised the role of emissions embedded in financial investment rather than just lifestyle and personal consumption.
"Climate action that doesn't address the outsized responsibilities of the wealthiest members of society risk missing one of the most powerful levers we have to reduce future harm," said senior author Carl-Friedrich Schleussner, head of the Integrated Climate Impacts Research Group at the International Institute for Applied Systems Analysis near Vienna.
Billionaires' tax
Owners of capital, he noted, could be held accountable for climate impacts through progressive taxes on wealth and carbon-intensive investments.
Earlier research has shown that taxing asset-related emissions is more equitable than broad carbon taxes, which tend to burden those on lower incomes.
Recent initiatives to increase taxes on the super-rich and multinationals have mostly stalled, especially since Donald Trump regained the White House.
Last year, Brazil - as host of the G20 - pushed for a two-percent tax on the net worth of individuals with more than $1 billion in assets.
Although G20 leaders agreed to "engage cooperatively to ensure that ultra-high-net-worth individuals are effectively taxed," there has been no follow-up to date.
In 2021, nearly 140 countries agreed on work toward a global corporate tax for multinational companies, with nearly half endorsing a minimum rate of 15 percent, but those talks have stalled as well.
Almost a third of the world's billionaires are from the United States - more than China, India and Germany combined, according to Forbes magazine.
According to anti-poverty NGO Oxfam, the richest 1 percent have accumulated $42 trillion in new wealth over the past decade.
It says the richest one percent have more wealth than the lowest 95 percent combined.
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These include flow cytometry to evaluate for large granular lymphocyte and paroxysmal nocturnal hemoglobinuria clone. Human leukocyte antigen typing offers clinical value if the patient is a hematopoietic cell transplant candidate. Because the patient in the present case is considered lower risk, she probably is not at this juncture. Recombinant fusion protein, such as luspatercept, is the most appropriate option for this patient, given its approval for the treatment of anemia in patients with lower-risk MDS-RS who have not responded to treatment with ESAs. In patients with lower-risk MDS and symptomatic anemia, treatment is usually guided by cytogenetic findings, serum EPO levels, and the presence of ring sideroblasts or SF3B1 mutations. For patients with del(5q) , lenalidomide remains the preferred treatment regardless of EPO level. For those with SF3B1 mutations or ring sideroblasts ≥ 15% (or ≥ 5% with a mutation), luspatercept is preferred, with imetelstat recommended if EPO is > 500 mU/mL and the patient is ineligible for ESAs. In patients without these features, ESAs plus granulocyte colony-stimulating factor or imetelstat may be considered on the basis of EPO levels, with follow-up based on response. Escalation to agents like ivosidenib or enasidenib is recommended only in the presence of IDH mutations. Neither hypomethylating agents or allogeneic transplant are included in this lower-risk anemia-focused treatment pathway. Further, intensive induction chemotherapy is not typically utilized in this setting.