The objective of this blog is to post images and news, that are published at other websites, that are concerned about the conditions of our the world oceans. It is also an english version SOS OCEANOS.We also write and publish relevant information and photographs of our region whenever is necessary people to know.
sexta-feira, 31 de dezembro de 2010
What triggers mass extinctions? Study shows how invasive species stop new life
ScienceDaily (2010-12-31) -- An influx of invasive species can stop the dominant natural process of new species formation and trigger mass extinction events, according to new research. The study of the collapse of Earth's marine life 378 to 375 million years ago suggests that the planet's current ecosystems, which are struggling with biodiversity loss, could meet a similar fate.
http://www.sciencedaily.com/releases/2010/12/101230100050.htm
sábado, 25 de dezembro de 2010
Growing hypoxic zones reduce habitat for billfish and tuna
Samples of surface skin slime are taken from the Atlantic sailfish to determine gender. (Credit: NOAA) |
ScienceDaily (2010-12-23) -- Billfish and tuna, important commercial and recreational fish species, may be more vulnerable to fishing pressure because of shrinking habitat, according to a new study. An expanding zone of low oxygen, known as a hypoxic zone, in the Atlantic Ocean is encroaching upon these species' preferred oxygen-abundant habitat, forcing them into shallower waters where they are more likely to be caught.
http://www.sciencedaily.com/releases/2010/12/101222162402.htm
terça-feira, 21 de dezembro de 2010
Ocean acidification changes nitrogen cycling in world seas
full article: http://www.sciencedaily.com/releases/2010/12/101220163258.htm
sexta-feira, 10 de dezembro de 2010
Cloud 'feedback' affects global climate and warming
sexta-feira, 3 de dezembro de 2010
'No fish left behind' approach leaves Earth with nowhere left to fish, study finds
http://www.sciencedaily.com/releases/2010/12/101202181122.htm
sexta-feira, 26 de novembro de 2010
UK sets up Chagos Islands marine reserve
Science reporter, BBC News
Conservationists say the area is a biodiversity hotspot |
sexta-feira, 19 de novembro de 2010
Busy microbial world discovered in deepest ocean crust ever explored
ScienceDaily (Nov. 19, 2010) — The first study to ever explore biological activity in the deepest layer of ocean crust has found bacteria with a remarkable range of capabilities, including eating hydrocarbons and natural gas, and "fixing" or storing carbon.
quarta-feira, 17 de novembro de 2010
Heat stress to Caribbean corals in 2005 worst on record; Caribbean reef ecosystems may not survive repeated stress
NOAA diver with a one square meter quadrat examining a bleached reef (Montastraea) colony in St. Croix, USVI in Oct., 2005. (Credit: NOAA) |
The study appears in PLoS ONE, an international, peer-reviewed, open-access, online publication.
sábado, 13 de novembro de 2010
New ocean acidification study shows added danger to already struggling coral reefs
Ocean acidification could compromise the successful fertilization, larval settlement and survivorship of Elkhorn corals, new research reveals. (Credit: Evan D'Alessandro, University of Miami) |
ScienceDaily (Nov. 13, 2010) — Over the next century, recruitment of new corals could drop by 73 percent, as rising carbon dioxide levels turn the oceans more acidic, suggests a new study led by scientists at the University of Miami Rosenstiel School of Marine and Atmospheric Science. The research findings reveal a new danger to the already threatened Caribbean and Florida reef Elkhorn corals.
Oceanography researchers discover toxic algae in open water
Microscopic image of Pseudo-nitzschia. (Credit: Image courtesy of Ross Del Rio) |
The findings were published in the Nov. 8 edition of the Proceedings of the National Academy of Sciences(PNAS).
sexta-feira, 12 de novembro de 2010
Extreme global warming in the ancient past
The image shows the the scientific drilling ship JOIDES Resolution docked in Hobart, Tasmania. (Credit: John Beck, IODP) |
full article at: http://www.sciencedaily.com/releases/2010/11/101110101313.htm
terça-feira, 26 de outubro de 2010
segunda-feira, 18 de outubro de 2010
quinta-feira, 14 de outubro de 2010
: New Report: Reducing Carbon Dioxide to 350 ppm Is Necessary to Avoid Climate Catastrophe
TIANJIN, China— Reducing carbon dioxide levels to 350 parts per million (ppm) in the Earth’s atmosphere is a necessary, viable step toward preventing catastrophic effects from global climate change, according to a new report. “Not Just a Number: Achieving a CO2 Concentration of 350 ppm or Less to Avoid Catastrophic Climate Impacts” was prepared by the Center for Biological Diversity and350.org to coincide with the international climate talks that opened this week in Tianjin, China.
“Climate change is happening much more quickly than predicted. Even seen in the most optimistic light, pledges made last year in Copenhagen would still lead to unacceptably dangerous levels of CO2 and set off a disastrous chain of events. We have to do better,” said Matt Vespa, a Center attorney and one of the report’s lead authors. “To preserve a planet resembling the one we rely on today, we must reduce atmospheric CO2 to less than 350 ppm. It’s an ambitious goal, but also crucial and achievable.”
Current CO2 levels are about 392 parts per million. Scientists predict that if changes aren’t made soon, it will be impossible to avoid some of the worst effects of global warming, including rising ocean levels, more extreme weather events, water shortages, accelerated species loss and disrupted economies and food supplies.
quarta-feira, 13 de outubro de 2010
Regional sea temperature rise and coral bleaching event in Western Caribbean
ScienceDaily (Oct. 13, 2010) — The Smithsonian Tropical Research Institute's Bocas del Toro Research Station and Galeta Point Marine Laboratory are reporting an anomalous sea temperature rise and a major coral bleaching event in the western Caribbean.
Dying Sponges: Abnormal sea temperatures not only affect corals, but also affect other reef organisms like these sponges. (Credit: Arcadio Castillo) |
terça-feira, 12 de outubro de 2010
Whale Poop Pumps Up Ocean Health
http://www.sciencedaily.com/releases/2010/10/101012101255.htm
A conceptual model of the whale pump. In the common concept of the biological pump, zooplankton feed in the euphotic zone and export nutrients via sinking fecal pellets, and vertical migration. Fish typically release nutrients at the same depth at which they feed. Excretion for marine mammals, tethered to the surface for respiration, is expected to be shallower in the water column than where they feed. (Credit: Peter Roopnarine, Joe Roman, James J. McCarthy. The Whale Pump: Marine Mammals Enhance Primary Productivity in a Coastal Basin. PLoS ONE, 2010; 5 (10): e13255 DOI: 10.1371/journal.pone.0013255)
quarta-feira, 6 de outubro de 2010
Climate change affects horseshoe crab numbers
ScienceDaily (2010-10-04) -- Having survived for more than 400 million years, the horseshoe crab is now under threat -- primarily due to overharvest and habitat destruction. However, climatic changes may also play a role, according to a new study.
Horseshoe crab. (Credit: Photo: University of Gothenburg) |
Full article at
http://www.sciencedaily.com/releases/2010/10/101004101330.htm
domingo, 3 de outubro de 2010
World's rivers in 'crisis state', report finds
Keep in mind that the water from rivers goes to the world´s oceans.
ScienceDaily (2010-10-01) -- The world's rivers, the single largest renewable water resource for humans and a crucible of aquatic biodiversity, are in a crisis of ominous proportions, according to a new global analysis.
sexta-feira, 1 de outubro de 2010
How Does Toxic Mercury Get into Fish?
The article below from WHOI has been sent to you by trajano@sosoceanos.org
http://www.whoi.edu/oceanus/viewArticle.do?id=79706
How Does Toxic Mercury Get into Fish?
Most everyone has heard by now that we should limit our consumption of certain fish because they accumulate high levels of toxic mercury. But nobody—not even scientists—knows how that toxic mercury gets into the ocean in the first place.
Here’s the mystery: Most of the mercury that enters the ocean from sources on land or air is just the element mercury, a form that poses little danger because living things can get rid of it quickly. The kind of mercury that accumulates to toxic levels in fish is called monomethylmercury, or simply methylmercury, because it has a methyl group, CH3, attached to the mercury atom.
The problem is that we don’t know where methylmercury comes from. Not nearly enough of it enters the ocean to account for the amounts we find in fish. Somewhere, somehow, something in the ocean itself is converting relatively harmless mercury into the much more dangerous methylated form. (See interactive of the mercury cycle.)
That’s the puzzle Carl Lamborg, a biogeochemist at Woods Hole Oceanographic Institution (WHOI), is trying to solve. Lamborg got hooked on mercury as a master’s degree student at the University of Michigan and then pursued his Ph.D. at the University of Connecticut with Bill Fitzgerald, one of the foremost experts on mercury in the ocean. Fitzgerald, who was the third student to graduate from the MIT/WHOI Joint Program and the first in chemical oceanography, devoted his career to mercury after seeing photographs in the 1970s of people poisoned by methylmercury dumped from a chemical plant into Minamata Bay, Japan. In one famous picture, originally published in Life magazine, a woman cradles her teenage daughter, who had been deformed by prenatal exposure to methylmercury. (The photographer, W. Eugene Smith, later withdrew this and other searing photos from public display at the request of the subjects and their families.)
Minamata Bay was one of the worst cases ever of methylmercury poisoning, but sadly, it was not unique.
“There was a lot of mercury dumped back in the day when folks were not sensitive to what was going on,” said Lamborg. “The buzzword that people use for that is ‘legacy mercury.’ Coastal sediments tend to be really elevated in mercury that was dumped there 30, 40, 50, 100 years ago as a result of some industry. And that might still be in play, because there’s worms and shellfish and things living in the mud, and they’re always sort of stirring it up.”
The big question
At Minamata Bay, the source of the methylmercury was clear. We also know the source of most of the elemental mercury in the ocean. Some comes from natural sources such as volcanic eruptions. About two-thirds comes from human activities. The biggest single source is the burning of fossil fuels, especially coal, which releases 40 tons of mercury a year into the air in the United States alone. From there, rainfall washes the mercury into the ocean.
We also discharge mercury-laden industrial effluents directly into rivers or the ocean. This is not just a scourge of modern life; Lamborg said a mercury mine in Slovenia has been dumping its wastewater into the Gulf of Trieste since Roman times.
But even large discharges such as that wouldn’t pose a major threat to human health if the mercury were not converted to methylmercury, which diffuses into phytoplankton and then passes up the food chain in ever-accumulating quantities. Large predator fish such as tuna, for example, contain about 100 million times as much methylmercury as the water surrounding them.
“Something like a shellfish, which is a filter feeder, that’s very close to the bottom of the food chain, is generally not as high in methylmercury as something like a tuna or a mackerel or swordfish or striped bass—all the fish, actually, that we really like to eat,” Lamborg said.
So where and how does the conversion of mercury to methylmercury take place? Lamborg said the process is probably biotic—done by living things. Beyond that, our knowledge is sketchy. We know that fish don’t methylate mercury, and phytoplankton and zooplankton probably don’t either.
However, some species of bacteria do produce methylmercury, as a byproduct of their respiration. This has been observed in bacteria living in seafloor sediments along coasts and on continental shelves. It might also occur in deep-ocean sediments, but no one has looked there yet.
In lieu of oxygen
A few centimeters down into the sediment, there’s so little oxygen that microbes living there must use anaerobic respiration. One common means is a chemical reaction called sulfate reduction, in which they use sulfate (SO42-) in surrounding seawater for respiration and excrete sulfide (S2-) into the water as a waste product. If seawater in porous spaces within the sediment also contains a lot of mercury, the stage is set for the production of methylmercury.
That’s because sulfide helps mercury get into cells. Most forms of mercury can’t pass through a cell membrane because they are bound to large molecules or because they carry a charge. But when positively charged mercury ions (Hg+2), the most common form of mercury in the ocean, meets negatively charged sulfide, the two bond. The resulting compound, HgS, is small and uncharged—just right to be able to pass into microbial cells.
Once inside, the mercury gets methylated. Scientists haven’t yet discovered the chemical reactions involved in this conversion, but soon after HgS enters bacterial cells, the cells release methylmercury. Some of the methylmercury diffuses out of the sediments into the open water. There, it is taken up by phytoplankton to begin its journey up the food chain.
But how much of the methylmercury made by bacteria in sediments finds its way into the water above? Is that the only source of the methylmercury that turns fish toxic?
Lamborg is skeptical of that idea. He thinks there has to be another source of methylmercury adding to the oceanic total.
“What I’ve been chewing on is the possibility that a lot of methylmercury is actually coming from within the water itself,” he said.
A mercury-rich layer of the ocean
Lamborg has found that there’s a layer of water in the ocean, between 100 and 400 meters thick, that contains high levels of methylmercury. It occurs at midwater depths—from 100 to 1,000 meters below the surface, depending on different locations in the ocean. He’s seen the high methylmercury layer in the relatively isolated Black Sea, the open ocean near the western coast of Africa, and the waters near Bermuda. What’s especially intriguing is that peak levels of methylmercury occur at depths where the amount of oxygen in the water drops sharply.
“This drop in oxygen is caused by all the plankton that are growing closer to the surface,” he said. “When they die, or when they’re eaten by other plankton, those dead cells or the poops of the other plankton sink down and rot. That rotting consumes oxygen.”
It’s possible that, like bacteria in sediments, any bacteria living in low-oxygen areas of the ocean also rely on sulfate for respiration and could be generating methylmercury in the midwater low-oxygen zone.
Lamborg is pursuing that hypothesis, but first he tested another possibility: whether methylmercury in the low-oxygen zone came from higher up in the water. Scientists studying phytoplankton have found that 20 to 40 percent of the mercury inside them is methylated. Lamborg wondered: As the phytoplankton or zooplankton that eat them die, sink, and get degraded, does any of that methylmercury get released back into the water and accumulate in midwater depths?
Catch a falling particle
To find out, Lamborg collected tiny particles that were sinking through the water and tested them for the presence of mercury and methylmercury. He caught the particles in sediment traps—polycarbonate tubes about 3 inches across and 2 feet long, that were suspended from a cable at 60 meters, 150 meters, and 500 meters below the surface.
Before deploying the traps, Lamborg filled each one with particle-free seawater. Then he added extra-salty brine that was so dense that it formed a distinct layer at the bottom of the tube, which traps the particles.
He left the traps in place for four days, then hauled them up and ran the brine through flat, round filters a bit bigger across than a quarter. There’s no doubt when a trap is successful at gathering material, said Lamborg; the fine brown residue left on the filters has an air of rotting fish. “They smell pretty bad,” he said. “It’s not like poop, but it’s definitely ‘eww!’ ”
Lamborg collected sinking particles at several locations during a research cruise across the Atlantic from Brazil to the coast of Namibia in 2007, and brought them back to his lab at WHOI for analysis.
Panning for mercury
To find out how much methylmercury fell into a trap, Lamborg converted all the mercury on the filter to elemental mercury. He then passed the sample over grains of sand that had been coated with gold. Only the mercury sticks to the gold; other chemicals don’t. Then Lamborg heated the gold-mercury amalgam to vaporize the mercury.
“This is the same process that people doing gold mining used to use,” Lamborg said. “You know panning for gold? You would squeeze some mercury in your pan and sluice it around, dump off the sediment, and then you would heat it up and burn off the mercury and leave the gold behind.”
In Lamborg’s version of the process, the gaseous mercury is the valuable product. It gets drawn into wiry Teflon tubes that take it to an atomic fluorescence spectrometer that determines how much mercury was in the sample. On a nearby table, mercury from a parallel sample is run through a gas chromatograph to determine what proportion of it was methylated.
“These are some of the most challenging samples to analyze that I’ve come across, because the samples are very small,” Lamborg said. “There’s very little material. The techniques we’re using can detect methylmercury in the femtomolar range.” One femtomole of methylmercury would be 0.000000000000215 grams per liter of seawater.
The samples contained elemental mercury, but so far, none of the samples from any of the three depths have shown substantial levels of methylmercury. It was present, but at lower levels than are found in phytoplankton—far too little to explain the levels of methylmercury seen in the midwater zone.
Next steps
If organisms in surface waters are not the source of methylmercury in the midwater layer, where does that methylmercury come from? Lamborg said it could be made by bacteria in sediments on the continental shelf and released into the water. Currents could sweep these methylmercury-rich waters off the shelves and into the open ocean at depths about the same as the midwater layer. Other researchers are exploring that possibility.
Lamborg, though, favors the notion that methylmercury found in midwaters is being made there, just as it is in sediments, by microbes that are reducing sulfate. He recently started working with microbiologist Tracy Mincer, a colleague in the WHOI Department of Marine Chemistry and Geochemistry, to identify the genes that bacteria use to methylate mercury. Their research could identify similar genes to look for in microbes in the low-oxygen midwater zone.
And he’s still interested in those sinking particles and what role they might play. Methylating microbes can’t do their thing unless they have mercury to work with, and Lamborg thinks the particles offer an efficient shuttle service for mercury that enters surface layers of the ocean from the atmosphere, ground water, or rivers.
“Mercury entering the ocean today is reaching that low-oxygen zone somehow,” he said. “These particles are still playing an important role in moving mercury from a part of the ocean where methylation doesn’t occur to a part of the ocean where it does.”
This research was supported by the National Science Foundation and the Andrew W. Mellon Foundation Awards for Innovative Research at WHOI.
segunda-feira, 27 de setembro de 2010
Planet Earth online: Mosses provide early warning of air pollution
Message:
Important issue from Planet Earth Online on how mosses can help monitoring air pollution.
Mosses provide early warning of air pollution
First detailed analysis of factors affecting nitrogen in mosses.
http://planetearth.nerc.ac.uk/news/story.aspx?id=819
domingo, 19 de setembro de 2010
sexta-feira, 17 de setembro de 2010
To Fertilize, or Not to Fertilize
The article below from WHOI has been sent to you by trajano@sosoceanos.org
http://www.whoi.edu/oceanus/viewArticle.do?id=37026
To Fertilize, or Not to Fertilize
Global warming is “unequivocal,” the Intergovernmental Panel on Climate Change (IPCC) reported in November 2007. Human actions—particularly the burning of fossil fuels—have dramatically raised carbon dioxide and other greenhouse gases in the atmosphere, leading our planet toward “abrupt or irreversible climate changes and impacts,’’ the IPCC said. New, stronger scientific evidence indicates that these impacts may be larger than projected and come sooner than previously expected.
The IPCC, representing scientists from all over the world, shared with Al Gore the 2007 Nobel Peace Prize, which helped ramp up public and political attention to the urgency of taking action on climate change. Meanwhile, some action has been spurred by a combination of international treaties such as the Kyoto Protocol, national policies, and economic forces. From 2005 to 2006, carbon-emissions trading markets tripled, from $10 billion to $30 billion worldwide.
All this has renewed interest in finding ways not only to reduce carbon dioxide emissions but also to remove excess carbon from the atmosphere and sequester it in land-based “sinks” (such as forests), or in the ocean. That has rekindled a spotlight on the oceans’ role in regulating carbon dioxide and climate on our planet.
In the constant exchange between air and sea, carbon dioxide gas enters the oceans and can turn into other inorganic carbon forms. Atmospheric carbon dioxide, an essential ingredient for photosynthesis, is also used by marine phytoplankton, the microscopic plants that account for about half of all the photosynthesis that occurs on Earth. When these phytoplankton die or are eaten, their organic carbon can sink and be sequestered in the deep sea.
In the 1990s, a scientist named John Martin promulgated the “iron hypothesis,” suggesting that if we add small amounts of iron, an essential nutrient, to certain ocean areas, we might turn up the knob on the oceans’ productivity, producing more phytoplankton and maybe decreasing the level of heat-trapping carbon dioxide gas in the atmosphere. Scientists have tested the iron hypothesis in laboratories and in the field for more than a decade. They have verified that iron can stimulate productivity, but it may not necessarily increase long-term ocean carbon storage. Now several companies are embarking on commercial ventures to fertilize the ocean and sell carbon credits for removing carbon dioxide from the atmosphere.
But surely a solution couldn’t be as simple as adding iron “fertilizer” on a large scale to the oceans? Even the most optimistic estimates suggest that ocean iron fertilization could compensate for only a small fraction of total human carbon emissions, and only if we fertilize vast tracts of the ocean. What would be the consequences to ocean ecology and chemistry? Who should regulate and verify an ocean iron fertilization project? Should commercial iron fertilization be allowed to proceed cautiously in a framework of scientific monitoring? Or should it be prohibited given the potential environmental harm and the inherent uncertainties involved in manipulating complex biological systems?
To explore these questions, we set out with a modest goal of bringing together a diverse group of natural and social scientists, policymakers, economists, legal experts, environmental groups, and journalists to spend two days in September 2007 discussing iron, carbon, and plankton in the oceans. We shared what we know about iron’s role in stimulating plankton blooms and increasing ocean carbon storage; about the impacts on the oceans’ ecosystems, chemistry, and circulation; about evidence revealing how the ocean and climate worked in the past; and about computer models that tell us something about how they may operate in the future. We also discussed who might be involved in regulating the high seas, and what economic markets were interested in ocean iron fertilization as a possible method to offset carbon emissions.
We also heard that we don’t understand all of the possible impacts, and we can’t yet predict the full range of consequences of larger-scale ocean iron manipulations. To varying degrees, this is true of all strategies for dealing with climate change: We will have to move forward with uncertainties, whether we simply do nothing or actively pursue some set of strategies.
To make intelligent choices among alternative strategies, we need to assess their likely costs, benefits, and uncertainties. Toward that end, we came together with many different perspectives on what we know and what we would like to know about ocean iron fertilization. We did not come together to approve or disapprove of any particular commercial or research plans. The articles in this volume of Oceanus assemble much of the research and many of the different perspectives on ocean iron fertilization that were presented at our conference.
We hope our conference and this collection of articles shed some light on ocean iron fertilization, an often misunderstood, oversold, and oversensationalized process that has been occurring naturally for millions of years. With new international regulations and public/private partnerships emerging to fund and possibly profit from ocean iron fertilization, the time may be right to pursue a middle ground of longer and larger scientific experiments to improve understanding of ocean iron fertilization and the oceans’ potential for storing carbon.
—Ken Buesseler and Scott Doney,
Marine Chemistry & Geochemistry Department,
and Hauke Kite-Powell, Marine Policy Center,
Woods Hole Oceanographic Institution
quarta-feira, 15 de setembro de 2010
Fw: [New post] Ocean acidification in high latitude seas
Ocean acidification in high latitude seasAnne-Marin Nisumaa | 15 September 2010 at 09:57 | Tags: review | Categories: Science | URL: http://wp.me/p2Y1l-1dc |
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[Shared Post] EPOCA: investigating the impacts of carbon dioxide on our oceans
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EPOCA: investigating the impacts of carbon dioxide on our oceansAnne-Marin Nisumaa | 15 September 2010 at 09:48 | Categories: Projects | URL: http://wp.me/p2Y1l-1da |
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Fw: [New post] Rob Dunbar: The threat of ocean acidification (video)
Rob Dunbar: The threat of ocean acidification (video)Anne-Marin Nisumaa | 14 September 2010 at 12:08 | Categories: Media coverage | URL: http://wp.me/p2Y1l-1d8 |
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segunda-feira, 13 de setembro de 2010
[Shared Post] Our changing world: The acid test: a feature on ocean acidification (audio)
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Our changing world: The acid test: a feature on ocean acidification (audio)Anne-Marin Nisumaa | 13 September 2010 at 11:20 | Categories: Media coverage | URL: http://wp.me/p2Y1l-1d2 |
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sexta-feira, 10 de setembro de 2010
The Oceans and The Phytoplankton, as Base of the Food chain
The dead sea: Global warming blamed for 40 per cent decline in the ocean's phytoplankton
By Steve Connor
Science Editor
Thursday, 29 July 2010
large bloom of phytoplankton - which has been described as 'the basis of life in the oceans' - floating in the north-eastern Atlantic, as seen from space - NASA http://www.independent.co.uk/environment/climate-change/the-dead-sea-global-warming-blamed-for-40-per-cent-decline-in-the-oceans-phytoplankton-2038074.html |