Saturday, October 27, 2012

Rockin' Teacher Materials: Don't Fall for Drugs!

This week has been Red Ribbon Week and there was a door decorating contest. I thought we would use our 'cut off the corners' trick to decorate the leaves for our?
'Don't Fall for Drugs' door. I have to say that the kids had a blast and came up with some very creative ways to remind us to stay away from drugs!

I made a variety of leaves on the Ellison die cutting machine and put out some scraps for the cut 'n paste fun! Check out these leaves!


Can you believe what drugs will do to your teeth?!?

hehehe Cracks me up!

Now, these are some groovy rockin' dudes!

If you haven't signed up for the {huge giveaway}, make sure you do! You can win 33 awesome teaching resources that are worth about $170! Wow!?

Happy Friday!

Source: http://rockinteachermaterials.blogspot.com/2012/10/dont-fall-for-drugs.html

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Friday, October 26, 2012

Moderate drinking decreases number of new brain cells

ScienceDaily (Oct. 24, 2012) ? Drinking a couple of glasses of wine each day has generally been considered a good way to promote cardiovascular and brain health. But a new Rutgers University study indicates that there is a fine line between moderate and binge drinking -- a risky behavior that can decrease the making of adult brain cells by as much as 40 percent.

In a study posted online and scheduled to be published in the journal Neuroscience on November 8, lead author Megan Anderson, a graduate student working with Tracey J. Shors, Professor II in Behavioral and Systems Neuroscience in the Department of Psychology, reported that moderate to binge drinking -- drinking less during the week and more on the weekends -- significantly reduces the structural integrity of the adult brain.

"Moderate drinking can become binge drinking without the person realizing it," said Anderson."In the short term there may not be any noticeable motor skills or overall functioning problems, but in the long term this type of behavior could have an adverse effect on learning and memory."

Shors and Anderson worked with postdoctoral fellow Miriam Nokia from the University of Jyvaskyla in Finland to model moderate to heavy drinking in humans using rodents that reached a blood alcohol level of 0.08 percent -- the legal driving limit in the United States and many other countries -- and found that brain cell production was affected negatively.

The researchers discovered that at this level of intoxication in rats -- comparable to about 3-4 drinks for women and five drinks for men -- the number of nerve cells in the hippocampus of the brain were reduced by nearly 40 percent compared to those in the abstinent group of rodents. The hippocampus is a part of the brain where the new neurons are made and is also known to be necessary for some types of new learning.

This level of alcohol intake was not enough to impair the motor skills of either male or female rats or prevent them from associative learning in the short-term. Still, Anderson said, th

is substantial decrease in brain cell numbers over time could have profound effects on the structural plasticity of the adult brain because these new cells communicate with other neurons to regulate brain health.

"If this area of your brain was affected every day over many months and years, eventually you might not be able to learn how to get somewhere new or to learn something new about your life," said Anderson, a graduate fellow in the Department of Neuroscience and Cell Biology. "It's something that you might not even be aware is occurring."

According to the National Institute of Alcohol Abuse and Alcoholism, men who drink 14 drinks a week and women who drink seven are considered at-risk drinkers. Although college students commonly binge drink, according to the institute, 70 percent of binge drinking episodes involved adults age 26 and older.

"This research indicates that social or daily drinking may be more harmful to brain health than what is now believed by the general public," she said.

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Story Source:

The above story is reprinted from materials provided by Rutgers University. The original article was written by Robin Lally.

Note: Materials may be edited for content and length. For further information, please contact the source cited above.


Journal Reference:

  1. M.L. Anderson, M.S. Nokia, K.P. Govindaraju, T.J. Shors. Moderate drinking? Alcohol consumption significantly decreases neurogenesis in the adult hippocampus. Neuroscience, 2012; 224: 202 DOI: 10.1016/j.neuroscience.2012.08.018

Note: If no author is given, the source is cited instead.

Disclaimer: This article is not intended to provide medical advice, diagnosis or treatment. Views expressed here do not necessarily reflect those of ScienceDaily or its staff.

Source: http://feeds.sciencedaily.com/~r/sciencedaily/most_popular/~3/0fIxn3FWv74/121024164759.htm

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Protecting the Child Tax Credit as fiscal cliff looms near

A crucial safety net for low- and moderate-income families is jeopardized as the nation hurtles towards the fiscal cliff, Maag writes.

By Elaine Maag,?Guest blogger / October 25, 2012

Tax payers search through tax forms at the Illinois Department of Revenue in Springfield, Ill., in this April 2010 file photo. As the nation approaches a fiscal cliff, the future of the Child Tax Credit is in question, Maag writes.

Seth Perlman/AP/File

Enlarge

The Child Tax Credit (CTC), a key piece of the safety net for low- and moderate-income families, is in jeopardy as the nation hurtles towards the fiscal cliff. Not only could the 2001 expansion of the credit die, but so could provisions in the 2009 stimulus that made the credit much more available to low-income families.

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My biggest fear is that Congress will cut a year-end deal that extends the 2001 expansion but lets the important 2009 changes die.

To explain what?s happening, here is a bit of history: Prior to 2001, the credit was $500 per child. Families whose credit exceeded the income tax they owed could get the balance as a refundable credit only if they had at least three children and paid enough payroll tax. The credit phased out for single parents with income over $75,000 and married couples with income over $110,000.

The 2001 act doubled the credit to $1,000 per child and broadened its refundability. Families could receive 15 cents of their credit for each dollar of earnings over $10,000. (The threshold was indexed for inflation and would be about $13,000 in 2013.) Stimulus legislation in 2008 and 2009 reduced the threshold to $8,500 and then to $3,000. The more generous refundability level enacted in 2009 is critically important for low-income families.

Of the $38.3 billion in total child credits that TPC estimates families will claim this year, $29.5 billion comes from the 2001 tax law and another $8.8 billion from the 2009 stimulus. Most of the 2001 increase will go to families in the middle income quintile and higher (see chart). Families with the lowest incomes will get less than 3 percent of the 2001 increase. In contrast, fully 60 percent of the benefits from the 2009 changes will go to families in the lowest income quintile.

As we near the fiscal cliff, Congress should keep in mind the entire package of CTC changes, noting that the 2009 ARRA changes matter most for very low-income families.

The Christian Science Monitor has assembled a diverse group of the best economy-related bloggers out there. Our guest bloggers are not employed or directed by the Monitor and the views expressed are the bloggers' own, as is responsibility for the content of their blogs. To contact us about a blogger, click here. To add or view a comment on a guest blog, please go to the blogger's own site by clicking on taxvox.taxpolicycenter.org.

Source: http://rss.csmonitor.com/~r/feeds/csm/~3/bC-zVJ_txdI/Protecting-the-Child-Tax-Credit-as-fiscal-cliff-looms-near

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Did bacteria spark evolution of multicellular life?

ScienceDaily (Oct. 23, 2012) ? Bacteria have a bad rap as agents of disease, but scientists are increasingly discovering their many benefits, such as maintaining a healthy gut.

A new study now suggests that bacteria may also have helped kick off one of the key events in evolution: the leap from one-celled organisms to many-celled organisms, a development that eventually led to all animals, including humans.

Published this month in the inaugural edition of the new online journal eLife, the study by University of California, Berkeley, and Harvard Medical School scientists involves choanoflagellates (aka "choanos"), the closest living relatives of animals. These microscopic, one-celled organisms sport a long tail or flagellum, tentacles for grabbing food and are members of the ocean's plankton community. As our closest living relative, choanos offer critical insights into the biology of their last common ancestor with animals, a unicellular or colonial organism that lived and died over 650 million years ago.

"Choanoflagellates evolved not long before the origin of animals and may help reveal how animals first evolved," said senior author Nicole King, UC Berkeley associate professor of molecular and cell biology.

Since first starting to study choanoflagellates as a post-doc, King has been trying to figure out why some choanoflagellates live their lives as single cells, while others form colonies. After years of dead ends, King and undergraduate researcher Richard Zuzow discovered accidentally that a previously unknown species of bacteria stimulates one choanoflagellate, Salpingoeca rosetta, to form colonies. Because bacteria were abundant in the oceans when animals first evolved, the finding that bacteria influence choano colony formation means it is plausible that bacteria also helped to stimulate multicellularity in the ancestors of animals.

"I would be surprised if bacteria did not influence animal origins, since most animals rely on signals from bacteria for some part of their biology," King said. "The interaction between bacteria and choanos that we discovered is interesting for evolutionary reasons, for understanding how bacteria interact with other organisms in the oceans, and potentially for discovering mechanisms by which our commensal bacteria are signaling to us."

No one is sure why choanoflagellates form colonies, said one of the study's lead authors, UC Berkeley post-doctoral fellow Rosanna Alegado. It may be an effective way of exploiting an abundant food source: instead of individual choanoflagellates rocketing around in search of bacteria to eat, they can form an efficient bacteria-eating "Death Star" that sits in the middle of its food source and chows down.

Whatever the reasons, colonies of unicellular organisms may have led the way to more permanent multicellular conglomerations, and eventually organisms composed of different cell types specialized for specific functions.

Sequencing the choanoflagellate genome

King's 12-year search for the trigger of choanoflagellate colony development was reignited in 2005 when she started to prime cultures of the choanoflagellate S. rosetta for a genome sequencing project. The sequencing of another choanoflagellate, the one-celled Monosiga brevicollis, gave some clues into animal origins, but she needed to compare its genome to that of a colony-forming choanoflagellate.

Surprisingly, when Zuzow tried to isolate the colony-forming choanoflagellate by adding antibiotics to the culture dish to kill off residual bacteria, strange things happened, said King.

"When he treated the culture with one cocktail of antibiotics, he saw a bloom of rosette colony formation," she said, referring to the rose petal-shaped colonies that were floating in the culture media. "When he treated with a different cocktail of antibiotics, that got rid of colony formation altogether."

That "rather mundane but serendipitous observation" led Zuzow and Alegado to investigate further and discover that only one specific bacterial species in the culture was stimulating colony formation. When other bacteria outnumbered it, or when antibiotics wiped it out, colony formation stopped. Alegado identified the colony-inducing bacteria as the new species, Algoriphagus machipongonensis. While she found that other bacteria in the Algoriphagus genus can also stimulate colony formation, other bacteria like E. coli, common in the human gut, cannot.

Working with Jon Clardy of Harvard Medical School, a natural products chemist, the two labs identified a molecule -- a fatty acid combined with a lipid that they called RIF-1 -- that sits on the surface of bacteria and is the colony development cue produced by the bacteria.

"This molecule may be betraying the presence of bacteria," Alegado said. "Bacteria just sit around blebbing off little membrane bubbles, and if one of them has this molecule, the choanoflagellates all of a sudden say, 'Aha, there are some bacteria around here.'"

The signal sets off a predetermined program in the choanoflagellate that leads to cell division and the development of rosettes, she said. The molecule RIF-1 is remarkably potent; choanos detect and respond to it at densities that are about one billionth that of the lowest concentration of sugar that humans can taste in water.

"We are investigating this molecule from many sides. How and why do bacteria make it? How do choanoflagellates respond to it, and why?" King said. She and her team also are analyzing the genome of the colony-forming choanoflagellate and the colony-inducing bacteria for clues to their interaction.

King hopes that this unexpected signaling between choanoflagellates and bacteria can yield insights into other ways in which bacteria influence biology, particularly the biology of the gut.

Coauthors with King, Alegado and Clardy are Zuzow, now a graduate student at Stanford University; Laura Brown, now a faculty member at Indiana University; Shugeng Cao and Renee Dermenjian of Harvard Medical School; and Stephen Fairclough of UC Berkeley. Dermenjian is now at Merck.

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Story Source:

The above story is reprinted from materials provided by University of California - Berkeley. The original article was written by Robert Sanders.

Note: Materials may be edited for content and length. For further information, please contact the source cited above.


Journal Reference:

  1. Rosanna A Alegado, Laura W Brown, Shugeng Cao, Renee K Dermenjian, Richard Zuzow, Stephen R Fairclough, Jon Clardy, Nicole King. A bacterial sulfonolipid triggers multicellular development in the closest living relatives of animals. eLife, 2012; 1 DOI: 10.7554/eLife.00013

Note: If no author is given, the source is cited instead.

Disclaimer: Views expressed in this article do not necessarily reflect those of ScienceDaily or its staff.

Source: http://feeds.sciencedaily.com/~r/sciencedaily/top_news/top_environment/~3/jc083uSCCwo/121024101758.htm

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Thursday, October 25, 2012

Platypus airboats have a Nexus S for a brain, we go eyes-on (video)

Platypus Android handsetpowered airboats eyeson video

Here's another extremely cool offshoot of the Carnegie Mellon Robotics Institute. Platypus LLC build autonomous robotic airboats that can be deployed for a wide range of usages including environmental data and monitoring hard-to-reach spots after natural disasters like flooding. The hull of the boat looks a good deal like a boogie board, built from polyurethane. On top, you'll find a propulsion fan assembly, just behind a hard plastic electronics compartment that houses internals like the Arduino board. That microcontroller communicates via Bluetooth with a smartphone that sits in the front of of the boat, safely cocooned inside an Otterbox case.

The models we saw this week were carrying Nexus S handsets -- relatively cheap solutions bought second-hand off of eBay. Just about any Android phone should do the trick, but in the case of this project, where phones can get wrenched loose or just outright pilfered, cheaper is certainly better. Platypus' proprietary app helps control the boat autonomously, using the handset's camera to provide situational awareness. Sensors mounted on the boat, meanwhile, offer up information on oxygen and PH levels, temperature and more.

Continue reading Platypus airboats have a Nexus S for a brain, we go eyes-on (video)

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Platypus airboats have a Nexus S for a brain, we go eyes-on (video) originally appeared on Engadget on Wed, 24 Oct 2012 15:11:00 EDT. Please see our terms for use of feeds.

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Source: http://www.engadget.com/2012/10/24/platypus-airboats-have-a-nexus-s-for-a-brain-we-go-eyes-on-vid/

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Wednesday, October 24, 2012

Auburn wants to play keep-away from Texas A&M, says Scot Loeffler (video)

AUBURN, Alabama ? Auburn needs to keep the ball away from Texas A&M quarterback Johnny Manziel, and Tigers' offensive coordinator Scot Loeffler hopes he has a plan to do it.

Texas A&M, which ran 104 plays against LSU last Saturday, visits Jordan-Hare Stadium this Saturday with the SEC's No. 1 offense.

?"To help our defense, we've got to keep our defense off the field," Loeffler said.

That means Auburn's offense will have to be a lot better to play keep-away from the Aggies. While Texas A&M is first in the SEC in offense, Auburn is last.

Auburn defensive coordinator Brian VanGorder says he figures his players will be busy either way.

"The biggest concern is tempo. They're so fast. It takes a player so much out of his routine," VanGorder says in this Tuesday video. He says more about the Aggies, his Tigers and linebacker Cassanova McKinzy after the linebacker made his first start last week (he's got more to learn, VanGorder says).?

In the meantime, Auburn is trying to turn around a 1-6 season.?

"I feel bad for our players, I feel bad for the Auburn people, however, we're going to continue to fight," Loeffler said. "It's a struggle, there's no question about it.

"You either pound the rock or run and hide. Our players haven't done that and our coaches haven't done that.

"I think this group will develop into a really good team. As this group matures, they're not going to forget this, and neither are we."

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Source: http://www.al.com/auburnfootball/index.ssf/2012/10/auburn_wants_to_play_keep-away.html

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Friday, October 19, 2012

Ubisoft announces Far Cry 3 mod for MineCraft - Video Games - Digit

If you?re a Minecraft nut who just loves his (or her) mods, then Ubisoft has something pretty damn exciting to offer. Ubisoft has announced that they will be putting out a Far Cry 3 mod out for Minecraft that will also include a texture pack. What you can expect from the free pack is a brilliant fusion of Minecraft with the Far Cry 3 universe, giving you the ability to explore terrain and such in the upcoming shooter.

Every aspect of the game will get modified, including the environment, weapons and tools to reflect those from Far Cry 3.

Ubisoft has said that you will also run into Pixelated versions of characters from Far Cry 3. Ubisoft has been revealing character details as their game gets closer to launch and now that we?ve seen some of the savages and tribe members, we can?t help but wonder whether it will be these characters who are included in the mod or some totally new characters.

The mod will be available on October 26 for free on the PC and the actual Far Cry 3 game should be hitting store shelves on December 4, 2012.

Source: http://www.thinkdigit.com/Gaming/Ubisoft-announces-Far-Cry-3-mod-for_11088.html

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