200 Protesters Block Building Entrance to Kick Off Harvard 'Heat Week' Demanding Divestment from Fossil Fuels
Harvard University will be feeling the heat this week. That's because April 12-17 was designated "Heat Week" by Divest Harvard, the student-led group which also includes alumni, faculty and friends, demanding that the university divest its $36 billion endowment—the largest of any university in the world—from funds that invest in fossil fuels.
According to the student newspaper the Harvard Crimson, the protest began 7:30 p.m. Sunday when about 200 supporters gathered in front of Massachusetts Hall, an administration building that houses the office of university president Drew Faust. That followed a packed rally at First Parish where speakers addressed the crowd and fired them up to march to Massachusetts Hall.
The paper described the scene:
"At the rally, climate activists, many of whom were accessorized in neon orange scarves, buttons and headbands, sang protest songs in support of the students blocking the Mass. Hall doors. Protest leaders including environmental activist Bill E. McKibben ’82, the leader of the environmental group 350.org and a former Crimson president, and former Colorado Sen. Tim Wirth spoke to the crowd, encouraging the members to support the blockade throughout the week."
HAPPENING NOW: @billmckibben, hundreds join the blockade at @Harvard. #HarvardHeatWeek #divest #WhoseSide pic.twitter.com/zgRM7CVd2w
— Divest Harvard (@DivestHarvard) April 13, 2015
"Climate change is moving quickly, and we need action now,” McKibben told the Crimson. “[The protest] is a chance for us to remind Harvard to do more than talk.”
Divest Harvard co-founder Chloe E. Maxmin, class of ’15, said that protestors were ready and willing to be arrested if it came to that. One member of the group was arrested last May for blocking a door at Massachusetts Hall.
Divest Harvard kicked off the week by releasing a statement that said, "Tonight Harvard students, faculty and alumni assembled in peaceful, civil disobedience around Massachusetts Hall to launch Harvard Heat Week—a week of action for fossil fuel divestment. As climate change threatens to become the worst humanitarian crisis that humans have ever faced, we ask all students to join us this week in the movement for climate justice. In this historic moment, Harvard confronts a choice that will influence its legacy for hundreds of years. Will it continue to endorse the fossil fuel industry’s destructive practices? Or will it act to ensure a livable future for young people, future generations, already-marginalized communities, and all those on the frontlines of climate chaos?"
The students from @DivestHarvard blocking Mass Hall introduce themselves to the crowd. Heroes. #harvardheatweek pic.twitter.com/6mYBfvlPZE
— Jamie Henn (@Agent350) April 13, 2015
The group announced the weeklong "Heat Week" protest in February, following a 24-hour occupation of Massachusetts Hall. It is an escalation of the tactics Divest Harvard has been deploying since it formed in 2012. Faust has dismissed their demands, saying that the university will instead address climate change through research and education. She also refused to hold an open meeting where anyone could ask questions about divestment.
"This direct action comes after two and a half years of interactions with an administration that avoids engagement with student activism at all costs," Divest Harvard reported in February. "So we began our sit-in in the hopes that we could bring our voices and urgency directly to the doorstop of President Faust. It worked: by mid-morning, she was compelled to respond–a first in our experience with the administration. Yet despite that minor victory, her words made it clear she had no sincere interest in working with us. Instead, she issued an ultimatum that was intended to cut short our direct action, and she called our presence and our passion 'coercive.'”
“Peaceful protest is absolutely a part of our campus and they have every right to peacefully protest. They don't have the right to stop university business,” Faust said in March.
“The administration has consistently ostracized Divest Harvard and used ever-changing statements about why they’re not divesting,” Maxmin told the Crimson. “We're actually not that radical. We’re not insane. We’re genuinely frightened for our futures and truly believe that Harvard is sponsoring some of that fear.”
Speakers throughout the week include:
- Reverend Lennox Yearwood (founder, Hip-Hop Caucus);
- Darren Aronofsky (‘91, film director);
- Bill McKibben (‘82, co-founder, 350.org);
- Ferrial Adam (Africa – Arab World Team Leader, 350.org)
- Koreti Tiumalu (Pacific Coordinator, 350.org)
- Former U.S. Senator Tim Wirth (‘61);
- Kelsey Wirth (‘92, founder, Mothers Out Front)
- Bob Massie (‘89, founder, Investor Network on Climate Risk);
- Todd Gitlin (‘63, Author, Professor Columbia University);
- Talia Rothstein (Divest Harvard Organizer);
- Ted Hamilton (Divest Harvard Organizer); and
- Jibreel Khazan (participant in the 1960 Greensboro Woolworth’s Civil
- Rights lunch counter sit-ins); with
- Performances by Melodeego
More than 1,100 Harvard alumni, including notable figures such as Natalie Portman, Cornel West, Al Gore, and Bevis Longstreth, have signed on to a petition urging the administration to divest its fossil fuel holdings, as well as 72 percent of undergraduate students supporting a referendum vote, more than 65,000 community members and more than 245 faculty members calling for divestment, according to Divest Harvard.
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By Ana Maldonado-Contreras
- Your gut is home to trillions of bacteria that are vital for keeping you healthy.
- Some of these microbes help to regulate the immune system.
- New research, which has not yet been peer-reviewed, shows the presence of certain bacteria in the gut may reveal which people are more vulnerable to a more severe case of COVID-19.
You may not know it, but you have an army of microbes living inside of you that are essential for fighting off threats, including the virus that causes COVID-19.
How Do Resident Bacteria Keep You Healthy?<p>Our immune defense is part of a complex biological response against harmful pathogens, such as viruses or bacteria. However, because our bodies are inhabited by trillions of mostly beneficial bacteria, virus and fungi, activation of our immune response is tightly regulated to distinguish between harmful and helpful microbes.</p><p>Our bacteria are spectacular companions diligently helping prime our immune system defenses to combat infections. A seminal study found that mice treated with antibiotics that eliminate bacteria in the gut exhibited an impaired immune response. These animals had low counts of virus-fighting white blood cells, weak antibody responses and poor production of a protein that is vital for <a href="https://doi.org/10.1073/pnas.1019378108" target="_blank">combating viral infection and modulating the immune response</a>.</p><p><a href="https://doi.org/10.1371/journal.pone.0184976" target="_blank" rel="noopener noreferrer">In another study</a>, mice were fed <em>Lactobacillus</em> bacteria, commonly used as probiotic in fermented food. These microbes reduced the severity of influenza infection. The <em>Lactobacillus</em>-treated mice did not lose weight and had only mild lung damage compared with untreated mice. Similarly, others have found that treatment of mice with <em>Lactobacillus</em> protects against different <a href="https://doi.org/10.1038/srep04638" target="_blank" rel="noopener noreferrer">subtypes of</a> <a href="https://doi.org/10.1038/s41598-017-17487-8" target="_blank" rel="noopener noreferrer">influenza</a> <a href="https://doi.org/10.1371/journal.ppat.1008072" target="_blank" rel="noopener noreferrer">virus</a> and human respiratory syncytial virus – the <a href="https://doi.org/10.1038/s41598-019-39602-7" target="_blank" rel="noopener noreferrer">major cause of viral bronchiolitis and pneumonia in children</a>.</p>
Chronic Disease and Microbes<p>Patients with chronic illnesses including Type 2 diabetes, obesity and cardiovascular disease exhibit a hyperactive immune system that fails to recognize a harmless stimulus and is linked to an altered gut microbiome.</p><p>In these chronic diseases, the gut microbiome lacks bacteria that activate <a href="https://doi.org/10.1126/science.1198469" target="_blank" rel="noopener noreferrer">immune cells</a> that block the response against harmless bacteria in our guts. Such alteration of the gut microbiome is also observed in <a href="https://doi.org/10.1073/pnas.1002601107" target="_blank" rel="noopener noreferrer">babies delivered by cesarean section</a>, individuals consuming a poor <a href="https://doi.org/10.1038/nature12820" target="_blank" rel="noopener noreferrer">diet</a> and the <a href="https://doi.org/10.1038/nature11053" target="_blank" rel="noopener noreferrer">elderly</a>.</p><p>In the U.S., 117 million individuals – about half the adult population – <a href="https://health.gov/our-work/food-nutrition/2015-2020-dietary-guidelines/guidelines/" target="_blank" rel="noopener noreferrer">suffer from Type 2 diabetes, obesity, cardiovascular disease or a combination of them</a>. That suggests that half of American adults carry a faulty microbiome army.</p><p>Research in my laboratory focuses on identifying gut bacteria that are critical for creating a balanced immune system, which fights life-threatening bacterial and viral infections, while tolerating the beneficial bacteria in and on us.</p><p>Given that diet affects the diversity of bacteria in the gut, <a href="https://www.umassmed.edu/nutrition/melody-trial-info/" target="_blank" rel="noopener noreferrer">my lab studies show how diet can be used</a> as a therapy for chronic diseases. Using different foods, people can shift their gut microbiome to one that boosts a healthy immune response.</p><p>A fraction of patients infected with SARS-CoV-2, the virus that causes COVID-19 disease, develop severe complications that require hospitalization in intensive care units. What do many of those patients have in common? <a href="https://www.cdc.gov/mmwr/volumes/69/wr/mm6912e2.htm" target="_blank" rel="noopener noreferrer">Old age</a> and chronic diet-related diseases like obesity, Type 2 diabetes and cardiovascular disease.</p><p><a href="http://doi.org/10.1016/j.jada.2008.12.019" target="_blank" rel="noopener noreferrer">Black and Latinx people are disproportionately affected by obesity, Type 2 diabetes and cardiovascular disease</a>, all of which are linked to poor nutrition. Thus, it is not a coincidence that <a href="https://www.cdc.gov/mmwr/volumes/69/wr/mm6933e1.htm" target="_blank" rel="noopener noreferrer">these groups have suffered more deaths from COVID-19</a> compared with whites. This is the case not only in the U.S. but also <a href="https://www.washingtonpost.com/world/europe/blacks-in-britain-are-four-times-as-likely-to-die-of-coronavirus-as-whites-data-show/2020/05/07/2dc76710-9067-11ea-9322-a29e75effc93_story.html" target="_blank" rel="noopener noreferrer">in Britain</a>.</p>
Discovering Microbes That Predict COVID-19 Severity<p>The COVID-19 pandemic has inspired me to shift my research and explore the role of the gut microbiome in the overly aggressive immune response against SARS-CoV-2 infection.</p><p>My colleagues and I have hypothesized that critically ill SARS-CoV-2 patients with conditions like obesity, Type 2 diabetes and cardiovascular disease exhibit an altered gut microbiome that aggravates <a href="https://theconversation.com/exercise-may-help-reduce-risk-of-deadly-covid-19-complication-ards-136922" target="_blank" rel="noopener noreferrer">acute respiratory distress syndrome</a>.</p><p>Acute respiratory distress syndrome, a life-threatening lung injury, in SARS-CoV-2 patients is thought to develop from a <a href="http://doi.org/10.1016/j.cytogfr.2020.05.003" target="_blank" rel="noopener noreferrer">fatal overreaction of the immune response</a> called a <a href="https://theconversation.com/blocking-the-deadly-cytokine-storm-is-a-vital-weapon-for-treating-covid-19-137690" target="_blank" rel="noopener noreferrer">cytokine storm</a> <a href="http://doi.org/10.1016/S2213-2600(20)30216-2" target="_blank" rel="noopener noreferrer">that causes an uncontrolled flood</a> <a href="http://doi.org/10.1016/S2213-2600(20)30216-2" target="_blank" rel="noopener noreferrer">of immune cells into the lungs</a>. In these patients, their own uncontrolled inflammatory immune response, rather than the virus itself, causes the <a href="http://doi.org/10.1007/s00134-020-05991-x" target="_blank" rel="noopener noreferrer">severe lung injury and multiorgan failures</a> that lead to death.</p><p>Several studies <a href="https://doi.org/10.1016/j.trsl.2020.08.004" target="_blank" rel="noopener noreferrer">described in one recent review</a> have identified an altered gut microbiome in patients with COVID-19. However, identification of specific bacteria within the microbiome that could predict COVID-19 severity is lacking.</p><p>To address this question, my colleagues and I recruited COVID-19 hospitalized patients with severe and moderate symptoms. We collected stool and saliva samples to determine whether bacteria within the gut and oral microbiome could predict COVID-19 severity. The identification of microbiome markers that can predict the clinical outcomes of COVID-19 disease is key to help prioritize patients needing urgent treatment.</p><p><a href="https://doi.org/10.1101/2021.01.05.20249061" target="_blank" rel="noopener noreferrer">We demonstrated</a>, in a paper which has not yet been peer reviewed, that the composition of the gut microbiome is the strongest predictor of COVID-19 severity compared to patient's clinical characteristics commonly used to do so. Specifically, we identified that the presence of a bacterium in the stool – called <em>Enterococcus faecalis</em>– was a robust predictor of COVID-19 severity. Not surprisingly, <em>Enterococcus faecalis</em> has been associated with <a href="https://doi.org/10.1053/j.gastro.2011.05.035" target="_blank" rel="noopener noreferrer">chronic</a> <a href="https://doi.org/10.1016/S0002-9440(10)61172-8" target="_blank" rel="noopener noreferrer">inflammation</a>.</p><p><em>Enterococcus faecalis</em> collected from feces can be grown outside of the body in clinical laboratories. Thus, an <em>E. faecalis</em> test might be a cost-effective, rapid and relatively easy way to identify patients who are likely to require more supportive care and therapeutic interventions to improve their chances of survival.</p><p>But it is not yet clear from our research what is the contribution of the altered microbiome in the immune response to SARS-CoV-2 infection. A recent study has shown that <a href="https://doi.org/10.1101/2020.12.11.416180" target="_blank" rel="noopener noreferrer">SARS-CoV-2 infection triggers an imbalance in immune cells</a> called <a href="https://doi.org/10.1111/imr.12170" target="_blank" rel="noopener noreferrer">T regulatory cells that are critical to immune balance</a>.</p><p>Bacteria from the gut microbiome are responsible for the <a href="https://doi.org/10.7554/eLife.30916.001" target="_blank" rel="noopener noreferrer">proper activation</a> <a href="https://doi.org/10.1126/science.1198469" target="_blank" rel="noopener noreferrer">of those T-regulatory</a> <a href="https://doi.org/10.1038/nri.2016.36" target="_blank" rel="noopener noreferrer">cells</a>. Thus, researchers like me need to take repeated patient stool, saliva and blood samples over a longer time frame to learn how the altered microbiome observed in COVID-19 patients can modulate COVID-19 disease severity, perhaps by altering the development of the T-regulatory cells.</p><p>As a Latina scientist investigating interactions between diet, microbiome and immunity, I must stress the importance of better policies to improve access to healthy foods, which lead to a healthier microbiome. It is also important to design culturally sensitive dietary interventions for Black and Latinx communities. While a good-quality diet might not prevent SARS-CoV-2 infection, it can treat the underlying conditions related to its severity.</p><p><em><a href="https://theconversation.com/profiles/ana-maldonado-contreras-1152969" target="_blank">Ana Maldonado-Contreras</a> is an assistant professor of Microbiology and Physiological Systems at the University of Massachusetts Medical School.</em></p><p><em>Disclosure statement: Ana Maldonado-Contreras receives funding from The Helmsley Charitable Trust and her work has been supported by the American Gastroenterological Association. She received The Charles A. King Trust Postdoctoral Research Fellowship. She is also member of the Diversity Committee of the American Gastroenterological Association.</em></p><p><em style="">Reposted with permission from <a href="https://theconversation.com/a-healthy-microbiome-builds-a-strong-immune-system-that-could-help-defeat-covid-19-145668" target="_blank" rel="noopener noreferrer" style="">The Conversation</a>. </em></p>
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