Friday 7 February 2014

Wierd animals may you don't know

1.Superb Bird of Paradise



2.Blob Fish

Image credits: coloribus.com | monsterfishworld.com

3.Red-lipped Batfish

(Image credits: imgur)

4.Umbonia Spinosa


These thorn bugs are related to cicadas, and use their beaks to pierce plant stems to feed upon their sap. Their strange appearance still poses many questions to scientists. (Image credits: Colin Hutton)

5.Glaucus Atlanticus




Also known as the blue dragon, this creature is a is a species of blue sea slug. You could find it in warm waters of the oceans, as it floats on the surface because of a gas-filled sac in its stomach. (Image credits: unknown | unknown |paulhypnos)



6.Venezuelan Poodle Moth



Discovered in Venezuela in 2009, this new species of alien-looking moth is still poorly explored. Waiting for more info about them! (Image credits: Arthur Anker | imgur)

7.The Bush Viper

Being a carnivore predator, the Bush Viper lives up in the trees of the tropical forests of Africa, and does most of its hunting at night. (Image credits: thegeneralmonk)

8.Narwhal

This toothed whale, found in the arctic, has been valued for over 1000 years by the Inuit people for its meat and ivory. The narwhal, however, is especially sensitive to the climate change. (Image credits: gowild.wwf.org.uk | Richard Thomas)

9.Thorny Dragon

Coloured in camouflaging shades of desert browns, this lizard has a “false” head, which he presents to his predators by dipping the real one. (Image credits: imgur | Christopher Watson)











10.The Maned Wolf


Image credits: imgur

Sunday 2 February 2014

Where Einstein Meets Hinduism ...


If someone asks you and me, “What time is it?” we would involuntarily check our wrist, or roll our head to the grandfather clock on our wall. But there was a man few decades back who would have snapped back, “You need time in relation to what?” That geeky German / American with innovative hairstyle and a thick moustache acknowledged as world’s most intellectual brain was none other than Albert Einstein. The old man in his”theory of relativity” went down to the pendulum of our grandfather’s clock and changed the definitions and the very foundations of the concept of time. He said that time is different for different people. “Well of course!” you might say “it is night in the USA right now while its day time here.” Please step back from that door in case your thinking is heading there. Do you think someone like Einstein would come up with a world renowned theory to prove that? What the genius meant was that what felt like 2 seconds to you might well be 2 days, 2 decades or maybe 200 years for someone else. “How can that be?” “Is he nuts to think something like that?”

I know, it is something difficult to imagine and understand, but needn’t be difficult to digest, after all even Joey the dumbest of all characters amongst the FRIENDS could assimilate the concept in one of his roles. Joey, acting as Victor on one of his stage performances in season 3 of FRIENDS gets on a spaceship to some BlogOn 7 planet in search of alternative fuels and is set to return back after 300 years. “And, when I return 300 years from now, you would have been long gone, but I wouldn’t have aged at all. So you tell your great, great granddaughter to look up to me. Because Adrian, baby, I would want to meet her.” This concept even decades after Einstein released his papers of “Time Dilation”, is found amongst comic series. People even today find it difficult to understand and easy to mock at. So guys, a standing ovation for the genius who could actually do an out of box thinking and come up with this theory. Come on, get up and applaud the man’s creativity and his efforts to prove that thinking.

But a Hindu would find a man in orange robes, with garland on his wrists and a pair of chaps in one of his hands that when stroked together add background music to his rhymes of, “Narayan, Narayan!” smiling at this discovery. Ladies and gentlemen meet Mr. Narad Muni, a divine sage in Hindu scriptures given the powers and the ability to travel between different planes and planets of the universe. If the Hindu mythology really exists then Narad Muni is the one who should know about this and the means to tackle with this kind of physics, mainly because the Hindu scriptures have professed this theory more than 5000 years back. “Now what was that?” Let me tell you a short story found in the epic of Mahabharata.

Once upon a time (isn’t this how a story should always start?) there was a kingdom beneath the oceans. It was ruled by a nice benevolent king called as Kakudmi who had an extremely beautiful daughter Revati. Kakudmi finding none amongst the earthlings as a capable life partner for his daughter, decided to consult Bramha the creator of the universe himself to find a capable groom for Revati. Since Lord Bramha was already engrossed in the music of the Gandharvas (yes, Gods rock too), Kakudmi decided to wait patiently for Gandharvas to finish their concert. After applauding their performance, Lord Bramha was amused to see King Kakudmi an earthling waiting at his door step with his daughter. Kakudmi sought consultations of the Lord Himself to find an appropriate groom for Revati. Bramha laughed at that moment and said, “O King, you have come to my door step. Here on this plane of the universe, time is different from what it is on earth. In the time that you were waiting here, 27 chaturyugs have passed by on earth. Your kingdom is long gone by and all of the grooms existing in your era on earth are now dead. All of your fore generations are already dead and an altogether different kind of human life is now growing itself on earth.”

Now let us dig deeper into this concept of Chaturyugs. 1 Chaturyug is actually 1 Mahayug made up of the 4 Yugs viz. the Satya Yug, Treta Yug, Dwapara Yug and the Kali Yug. 1 Yug equals to 432,000 human years. But the Hindu scriptures shaking hands with Einstein’s theory of relativity assert that these 432,000 human years are nothing but 0.01% of 1 day of Lord Bramha.




While 1 Maha Yug is 0.1% of Bramha’s day. So if you calculate backwards, 27 Chaturyugs (27 Maha Yugs) roughly turn out to be 78 minutes of Bramha’s day and that is the time King Kakudmi was waiting at Bramha’s doorstep with his daughter while the earth below spinning itself while revolving around the sun successfully completed 432,000*10*27 years of its life (1 Maha Yug = 10 Yugs). I am sure Einstein must have applauded this story. Now what happens later to King Kakudmi?

Lord Brahma assures him that the Lords themselves are now set to take an Avatar on the earth and thus you can marry this pure and pious Revati to one of them. King Kakudmi after setting back on earth finds a complete different picture from the time he left. Not just that the landscape and the places have changed, but the striking difference is the change in the human race itself. Instead of progressing, the human race has degraded itself. People now are that of lower intellectual and physical capabilities. But then comes Lord Balaram, the brother of Lord Krishna himself who is one capable person to marry Revati. So as per Brahma’s suggestions, Kakudmi marries Revati to Balaram.

This Yug philisophy is very much in sync with the Greek mythology where the Greeks have divided the life of human race into 4 ages viz. the Golden Age, the Silver Age, the Bronze age and the Iron Age. The Greeks profess that humans have degraded way of life from the Golden Age to the Iron Age. Each of the ages can be related to each of the Yugs in the Hindu philosophy. So when the Greeks say that we are now living in the Iron Age, Hindus christen the current time as the Kali Yug. The definitions and the descriptions of each of these Yugs do go hand in hand with the Greek Ages.

The difference that I would notice in the philosophies is that Hinduism drags the concept further to a cycle of Maha Yugs that come and go every now and then. And all of these 432,000*10 human years are nothing but few minutes of Lord Brahma. As per the calculations made in the Hindu scriptures, we are currently living in the 51st year of Lord Brahma and Lord Brahma along with this materialistic Brahmanda or today what we call as the universe, is set to live and exist for another 49 years. Ah well, excuse me, ‘Ahem!!’ 49 Brahma’s years.]

got from== (http://inimish.blogspot.in/2010/10/where-einstein-meets-hinduism.html)

सफलता की उड़ान : GSLV D5 और स्वदेशी क्रायोजेनिक इंजन



GSLV D5 प्रक्षेपण स्थल पर


भारतीय अंतरिक्ष अनुसंधान संगठन (इसरो) ने रविवार को जियोसिनक्रोनस सैटेलाइट लॉन्च व्हीकल (भू-स्थैतिक उपग्रह प्रक्षेपण वाहन) यानी जीएसएलवी डी-5 (GSLV D5)का सफल प्रक्षेपण किया जो इस लिहाज़ से अहम था कि भारत का अपना क्रायोजेनिक इंजन लगा हुआ था। जीएसएलवी डी-5 को रविवार शाम 4।18 बजे श्रीहरिकोटा अंतरिक्ष केंद्र से प्रक्षेपित किया गया था। स्वदेशी क्रायोजेनिक इंजन वाले जीएसएलवी डी-5 ने जीसैट-14 संचार उपग्रह को सफलतापूर्व उसकी कक्षा में स्थापित कर दिया।
GSLV D5 प्रक्षेपण स्थल परGSLV D5 प्रक्षेपण स्थल परये वही इंजन है जिसे भारत को विकसित करने में बीस वर्ष का समय लगा, जिसकी तकनीक को भारत अपने पड़ोसी देश रूस से हासिल करना चाहता था। लेकिन अमरीका के दबाव में रूस ने भारत को ये तकनीक नहीं दी थी। बीस वर्ष बाद ही सही भारत ने क्रायोजेनिक इंजन की तकनीक में महारथ हासिल कर ली है। इस तकनीक का महत्व इस तथ्य में निहित है कि दो हज़ार किलो वज़नी उपग्रहों को प्रक्षेपित करने के लिए क्रायोजेनिक इंजन की सख़्त ज़रूरत पड़ती है। इसकी वजह ये है कि इसी इंजन से वो ताक़त मिलती है, जिसके बूते किसी उपग्रह को 36,000 किलोमीटर दूर स्थित कक्षा में सफलतापूर्वक स्थापित किया जाता है। इस सफल प्रक्षेपण के साथ ही ये कहा जा सकता है कि भारत ने अंतरिक्ष विज्ञान की दुनिया में अब हर तरह की उपलब्धि हासिल कर ली है।
इस रॉकेट के सफल प्रक्षेपण से दूसरे देशों के संचार उपग्रह भी भारत के लॉन्च पैड से छोड़े जा सकेंगे। इसकी कामयाबी इसलिए भी अहम है क्योंकि पिछले “20 साल में कोई देश ऐसा नहीं है” जिसने क्रायोजेनिक तकनीक का विकास किया हो।
भारत का छोटा रॉकेट पीएसएलवी (पोलर सैटेलाइट लॉन्च व्हीकल PSLV) यानी ध्रुवीय प्रक्षेपण यान बहुत क़ामयाब है। भारत अपने उपग्रह ख़ुद बना रहा है। क्रायोजनिक इंजन भारत के संचार उपग्रहों को भी प्रक्षेपित करेगा। भारत जब अपना चंद्रयान-2 मिशन आरंभ करेगा, उसके लिए भी जीएसएलवी की ज़रूरत होगी।
महत्वपूर्ण तथ्य
महत्वपूर्ण तथ्य

GSLV D5 महत्वपूर्ण तथ्य

  1. ये भारत का सबसे बड़ा राकेट है और इससे भारत को काफी उम्मीदें हैं।
  2. ये राकेट 49 मीटर ऊंचा है। मतलब 17 मंजिली बिल्डिंग के बराबर इसकी ऊंचाई है।
  3. करीब 419 टन का इसका वजन है। यह वजह 80 व्यस्क हाथियों के वजन के बराबर है।
  4. भारत को इसकी काफी सख्त ज़रूरत है क्योंकि संचार संबंधी उपग्रह को छोड़ने में इसी राकेट से मदद मिलेगी। अगर भारत इसके प्रक्षेपण में कामयाब हो जाता है तो वो अपने संचार उपग्रहों को इस राकेट से छोड़ पाएगा।
  5. इससे काफी धन बचेगा क्योंकि अभी भारत इस काम के लिए फ्रांस के एक राकेट का इस्तेमाल करता है। इसके लिए भारत को कम से कम दोगुना कीमत चुकानी पड़ती है।
  6. अगर इस राकेट का प्रक्षेपण कई बार सफल हो जाता है तो आप दुनिया भर से व्यावसायिक काम पा सकते है। दूसरे देशों के संचार उपग्रह भारत के लांच पैड से छोड़े जा सकेंगे।
  7. इस राकेट के तीसरे चरण में एक क्रायोजेनिक इंजन का इस्तेमाल हो रहा है। क्रायोजेनिक इंजन में तरल हाइड्रोजन और तरल ऑक्सीजन का इस्तेमाल होता है, जो बरफ से भी बहुत कम तापमान पर काम करती है।
  8. ये तकनीकी आज 20 साल पहले भारत को देने से इनकार की गई थी। अमरीका के दबाव में रूस ने इनकार किया था।
  9. तब से भारत इस तकनीकी के विकास में लगा है। जीएसएलवी की इस उड़ान में जो क्रायोजेनिक इंजन लगा है वो भारत का अपना बनाया हुआ है।
  10. इस प्रक्षेपण की कामयाबी बहुत ज़रूरी है। उपग्रह से अधिक अहमियत क्रायोजेनिक इंजन की है।

क्रायोजेनिक इंजन क्या है?

  1. क्रायोजेनिक तकनीक को ‘निम्नतापकी’ कहा जाता है, जिसका ताप -0 डिग्री से -150 डिग्री सेल्सियस होता है।
  2. ‘क्रायो’ यूनानी शब्द ‘क्रायोस’ से बना है, जिसका अर्थ ‘बर्फ जैसा ठण्डा’ है।
  3. क्रायोजेनिक तकनीक का मुख्य प्रयोग रॉकेटों में किया जाता है, जहाँ ईधनों को क्रायोजेनिक तकनीक से तरल अवस्था में प्राप्त कर लिया जाता है।
  4. इस तकनीक में द्रव हाइड्रोजन एवं द्रव ऑक्सीजन का प्रयोग किया जाता है।
सफलता की उडान
सफलता की उडान
किसी राकेट को अंतरिक्ष में प्रक्षेपित करने के दौरान उसका ईंधन भी साथ में ले जाना पड़ता है। ऐसे में सबसे हल्का ईंधन तरल हाईड्रोजन और तरल ऑक्सीजन है और उसे जलाने पर सबसे अधिक ऊर्जा मिलती है। मुख्य बात यह है कि राकेट कितनी तेजी से जा रहा है और राकेट के साथ जितना कम वजन होगा वो उतनी अधिक दूर तक जा सकेगा।
क्रायोजेनिक इंजन शून्य से बहुत नीचे यानी क्रायोजेनिक तापमान पर काम करते हैं। ऋण 238 डिग्री फॉरेनहाइट (-238′F) को क्रायोजेनिक तापमान कहा जाता है। इस तापमान पर क्रायोजेनिक इंजन का ईंधन ऑक्सीजन और हाइड्रोजन गैसें तरल यानी द्रव बन जाती हैं। द्रव ऑक्सीजन और द्रव हाइड्रोजन को क्रायोजेनिक इंजन में जलाया जाता है। द्रव ईंधन जलने से इतनी ऊर्जा पैदा होती है जिससे क्रायोजेनिक इंजन को 4।4 किलोमीटर प्रति सेकेंड की रफ्तार मिल जाती है।
क्रायोजेनिक इंजन की तकनीक का विकास द्वितीय विश्वयुद्ध के दौरान हुआ। तब सबसे ज्यादा ऊर्जा पैदा करने वाले और आसानी से मुहैया ऑक्सीजन और हाइड्रोजन को ईंधन के तौर पर सबसे बेहतर पाया गया। मुश्किल ये थी इंजन में ये गैस के तौर पर इस्तेमाल नहीं हो सकती थीं, क्योंकि तब उन्हें रखने के लिए इंजन बड़ा बनाना पड़ता, जबकि रॉकेट उड़ाने के लिए इसका छोटा होना जरूरी शर्त है।
जीसैट-14 भारत का 23 वां भूस्थिर संचार उपग्रह है। जीसैट-14 के चार पूर्ववर्तियों का प्रक्षेपण जीएसएलवी ने 2001, 2003, 2004 और 2007 में किया था। जीसैट-14 भारत के नौ ऑपरेशनल भूस्थिर उपग्रहों के समूह में शामिल होगा। इस मिशन का प्राथमिक उद्देश्य विस्तारित सी और केयू-बैंड ट्रांसपोंडरों की अंतर्कक्षा क्षमता को बढ़ाना और नये प्रयोगों के लिए मंच प्रदान करना है। जीसैट-14 को 74 डिग्री पूर्वी देशांतर पर स्थापित किया जाएगा और इनसैट-3 सी, इनसैट-4 सीआर और कल्पना-1 उपग्रहों के साथ स्थित होगा। जीसैट-14 पर मौजूद 12 संचार ट्रांसपोंडर इनसैट, जीसैट प्रणाली की क्षमता को और बढ़ाएंगे।
जीसैट-14 भारत का 23 वां भूस्थिर संचार उपग्रह है। जीसैट-14 के चार पूर्ववर्तियों का प्रक्षेपण जीएसएलवी ने 2001, 2003, 2004 और 2007 में किया था। जीसैट-14 भारत के नौ ऑपरेशनल भूस्थिर उपग्रहों के समूह में शामिल होगा। इस मिशन का प्राथमिक उद्देश्य विस्तारित सी और केयू-बैंड ट्रांसपोंडरों की अंतर्कक्षा क्षमता को बढ़ाना और नये प्रयोगों के लिए मंच प्रदान करना है। जीसैट-14 को 74 डिग्री पूर्वी देशांतर पर स्थापित किया जाएगा और इनसैट-3 सी,  इनसैट-4 सीआर और कल्पना-1 उपग्रहों के साथ स्थित होगा। जीसैट-14 पर मौजूद 12 संचार ट्रांसपोंडर इनसैट, जीसैट प्रणाली की क्षमता को और बढ़ाएंगे।
भूस्थिर उपग्रह प्रक्षेपण यान में प्रयुक्त होने वाली द्रव्य ईंधन चालित इंजन में ईंधन बहुत कम तापमान पर भरा जाता है, इसलिए ऐसे इंजन तुषारजनिक रॉकेट इंजन (क्रायोजेनिक रॉकेट इंजिन) कहलाते हैं। इस तरह के रॉकेट इंजन में अत्यधिक ठंडी और द्रवीकृत गैसों को ईंधन और ऑक्सीकारक के रूप में प्रयोग किया जाता है। इस इंजन में हाइड्रोजन और ईंधन क्रमश: ईंधन और ऑक्सीकारक का कार्य करते हैं। ठोस ईंधन की अपेक्षा यह कई गुना शक्तिशाली सिद्ध होते हैं और रॉकेट को बूस्ट देते हैं। विशेषकर लंबी दूरी और भारी रॉकेटों के लिए यह तकनीक आवश्यक होती है।
क्रायोजेनिक इंजन के प्रणोद में तापमान बहुत ऊंचा (2000 डिग्री सेल्सियस से अधिक) होता है। अत: ऐसे में सर्वाधिक प्राथमिक कार्य अत्यंत विपरीत तापमानों पर इंजन व्यवस्था बनाए रखने की क्षमता अर्जित करना होता है। क्रायोजेनिक इंजनों में -253डिग्री सेल्सियस से लेकर 2000 डिग्री सेल्सियस तक का उतार-चढ़ाव होता है, इसलिए प्रणोद(थ्रस्ट) चैंबरों, टर्बाइनों और ईंधन के सिलेंडरों के लिए कुछ विशेष प्रकार की मिश्र-धातु की आवश्यकता होती है। भारतीय अंतरिक्ष अनुसंधान संगठन (इसरो) ने बहुत कम तापमान को आसानी से झेल सकने वाली मिश्रधातु विकसित कर ली है।
अन्य द्रव्य प्रणोदकों की तुलना में क्रायोजेनिक द्रव्य प्रणोदकों का प्रयोग कठिन होता है। इसकी मुख्य कठिनाई यह है कि ये बहुत जल्दी वाष्प बन जाते हैं। इन्हें अन्य द्रव प्रणोदकों की तरह रॉकेट खंडों में नहीं भरा जा सकता। क्रायोजेनिक इंजन के टरबाइन और पंप जो ईंधन और ऑक्सीकारक दोनों को दहन कक्ष में पहुंचाते हैं, को भी खास किस्म के मिश्रधातु से बनाया जाता है। द्रव हाइड्रोजन और द्रव ऑक्सीजन को दहन कक्ष तक पहुंचाने में जरा सी भी गलती होने पर कई करोड़ रुपए की लागत से बना जीएसएलवी रॉकेट रास्ते में जल सकता है। इसके अलावा दहन के पूर्व गैसों (हाइड्रोजन और ऑक्सीजन) को सही अनुपात में मिश्रित करना, सही समय पर दहन प्रारंभ करना, उनके दबावों को नियंत्रित करना, पूरे तंत्र को गर्म होने से रोकना आदि।
इस तकनीक का महत्व इस तथ्य में निहित है कि दो हज़ार किलो वज़नी उपग्रहों को प्रक्षेपित करने के लिए क्रायोजेनिक इंजन की सख़्त ज़रूरत पड़ती है। इसकी वजह ये है कि इसी इंजन से वो ताक़त मिलती है, जिसके बूते किसी उपग्रह को 36,000 किलोमीटर दूर स्थित कक्षा में सफलतापूर्वक स्थापित किया जाता है। इस सफल प्रक्षेपण के साथ ही ये कहा जा सकता है कि भारत ने अंतरिक्ष विज्ञान की दुनिया में अब हर तरह की उपलब्धि हासिल कर ली है।

Wednesday 15 January 2014

ACID RAIN


WHAT IS ACID RAIN?


Acid rain is the common name for acidic deposits that fall to Earth from the atmosphere. The term was coined in 1872 by the Scottish chemist Robert Angus Smith (1817–1884) to describe the acidic precipitation in Manchester, England. In the twenty-first century scientists study both wet and dry acidic deposits. Even though there are natural sources of acid in the atmosphere, acid rain is primarily caused by emissions of sulfur dioxide (SO2) and nitrous oxide (N2 O) from electric utilities burning fossil fuels, especially coal. These chemicals are converted to sulfuric acid and nitric acid in the atmosphere and can be carried by the winds for many miles from where the original emissions took place. (See Figure 5.1.) Other chemicals contributing to acid rain include volatile organic compounds (VOCs). These are carbon-containing chemicals that easily become vapors or gases. VOC sources include paint thinners, degreasers, and other solvents and burning fuels such as coal, natural gas, gasoline, and wood.

Wet deposition occurs when the acid falls in rain, snow, or ice. Dry deposition is caused by tiny particles (or particulates) in combustion emissions. They may stay dry as they fall or pollute cloud water and precipitation. Moist deposition occurs when the acid is trapped in cloud or fog droplets. This is most common at high altitudes and in coastal areas. Whatever its form, acid rain can create dangerously high levels of acidic impurities in water, soil, and plants.

Measuring Acid Rain
The acidity of any solution is measured on a potential hydrogen (pH) scale numbered from zero to fourteen, with a pH value of seven considered neutral. (See Figure 5.2.) Values higher than seven are considered more alkaline or basic (the pH of baking soda is eight); values lower than seven are considered acidic (the pH of lemon juice is two). The pH scale is a logarithmic measure. This means that every pH change of one is a tenfold change in acid content. Therefore, a decrease from pH seven to pH six is a tenfold increase in acidity; a drop from pH seven to pH five is a one hundredfold increase in acidity; and a drop from pH seven to pH
four is a one thousandfold increase.

Pure, distilled water has a neutral pH of seven. Normal rainfall has a pH value of about 5.6. It is slightly acidic because it accumulates naturally occurring sulfur oxides (SOx) and nitrogen oxides (NOx) as it passes through the atmosphere. Acid rain has a pH of less than 5.6.

Figure 5.3 shows the average rainfall pH measured during 2005 at various locations around the country by the National Atmospheric Deposition Program (NADP), a cooperative project between many state and federal government agencies and private entities. Rainfall was most acidic in the mid-Atlantic region and upper Southeast, particularly Ohio, Pennsylvania, West Virginia, Maryland, Delaware, Virginia, eastern Tennessee, and Kentucky. The areas with the lowest rainfall pH contain some of the country's most sensitive natural resources, such as the Appalachian Mountains, the Adirondack Mountains, Chesapeake Bay, and Great Smoky Mountains National Park. Overall, precipitation is much more acidic in the eastern United States than in the western United States because of a variety of natural and anthropogenic (human-caused) factors that are discussed below.

SOURCES OF SULFATE AND NITRATE IN THE ATMOSPHERE
Natural Sources
Natural sources of sulfate in the atmosphere include ocean spray, volcanic emissions, and readily oxidized hydrogen sulfide, which is released from the decomposition of organic matter found in the Earth. Natural sources of nitrogen or nitrates include NOx produced by micro-organisms in soils, by lightning during thunderstorms,

FIGURE 5.1

and by forest fires. Scientists generally speculate that one-third of the sulfur and nitrogen emissions in the United States comes from these natural sources. (This is a rough estimate as there is no way to measure natural emissions as opposed to those that are manmade.)

Sources Caused by Human Activity
According to the U.S. Environmental Protection Agency (EPA), in "What Is Acid Rain?" (June 8, 2007, http://www.epa.gov/acidrain/what/index.html), the primary anthropogenic contributors to acid rain are SO2 and NOx, resulting from the burning of fossil fuels, such as coal, oil, and natural gas.

The EPA notes in "Clearinghouse for Inventories and Emissions Factors" (http://www.epa.gov/ttn/chief/trends/trends06/nationaltier1upto2006basedon2002finalv2.1.xls) that approximately 70% of SO2 emissions produced in 2006 were because of fuel combustion by fossil-fueled electric utilities. Fuel combustion at industrial facilities contributed another 13%. Lesser sources included transportation vehicles and industrial processes. Highway vehicles were the primary source of NOx emissions, accounting for 36% of the total in 2006. Off-highway vehicles (such as bulldozers) contributed 22%. Fuel combustion in power plants was another major source,

FIGURE 5.2

accounting for 20% of the total. Lesser sources included industrial processes and waste disposal and recycling

NATURAL FACTORS THAT AFFECT ACID RAIN DEPOSITION
Major natural factors contributing to the impact of acid rain on an area include air movement, climate, and topography and geology. Transport systems—primarily the movement of air—distribute acid emissions in definite patterns around the planet. The movement of air masses transports emitted pollutants many miles, during which the pollutants are transformed into sulfuric and nitric acid by mixing with clouds of water vapor.

FIGURE 5.3

In drier climates, such as those of the western United States, windblown alkaline dust moves more freely through the air and tends to neutralize atmospheric acidity. The effects of acid rain can be greatly reduced by the presence of basic (also called alkali) substances. Sodium, potassium, and calcium are examples of basic chemicals. When a basic and an acid chemical come into contact, they react chemically and neutralize each other. By contrast, in more humid climates where there is less dust, such as along the eastern seaboard, precipitation is more acidic.

Areas most sensitive to acid rain contain hard, crystalline bedrock and thin surface soils. When no alkaline-buffering particles are in the soil, runoff from rainfall directly affects surface waters, such as mountain streams. In contrast, a thick soil covering or soil with a high buffering capacity, such as flat land, neutralizes acid rain better. Lakes tend to be most susceptible to acid rain because of low alkaline content in lake beds. A lake's depth, its watershed (the area draining into the lake), and the amount of time the water has been in the lake are also factors.

EFFECTS OF ACID RAIN ON THE ENVIRONMENT
In nature the combination of rain and oxides is part of a natural balance that nourishes plants and aquatic life. However, when the balance is upset by acid rain, the results to the environment can be harmful and destructive. (See Table 5.1.)

Aquatic Systems
Even though pH levels vary considerably from one body of water to another, a typical pH range for the lakes and rivers in the United States is six to eight. Low pH levels kill fish, their eggs, and fish food organisms. The

TABLE 5.1

Effects of acid rain on human health and selected ecosystems and anticipated recovery benefits
Human health and ecosystem Effects Recovery benefits
SOURCE: "Appendix I. Effect of Acid Rain on Human Health and Selected Ecosystems and Anticipated Recovery Benefits," in Acid Rain: Emissions Trends and Effects in the Eastern United States, U.S. General Accounting Office, March 2000, http://www.gao.gov/archive/2000/rc00047.pdf (accessed July 27, 2007)
Human health In the atmosphere, sulfur dioxide and nitrogen oxides become sulfate and nitrate aerosols, which increase morbidity and mortality from lung disorders, such as asthma and bronchitis, and impacts to the cardiovascular system. Decrease emergency room visits, hospital admissions, and deaths.
Surface waters Acidic surface waters decrease the survivability of animal life in lakes and streams and in the more severe instances eliminate some or all types of fish and other organisms. Reduce the acidic levels of surface waters and restore animal life to the more severely damaged lakes and streams.
Forests Acid deposition contributes to forest degradation by impairing trees' growth and increasing their susceptibility to winter injury, insect infestation, and drought. It also causes leaching and depletion of natural nutrients in forest soil. Reduce stress on trees, thereby reducing the effects of winter injury, insect infestation, and drought, and reduce the leaching of soil nutrients, thereby improving overall forest health.
Materials Acid deposition contributes to the corrosion and deterioration of buildings, cultural objects, and cars, which decreases their value and increases costs of correcting and repairing damage. Reduce the damage to buildings, cultural objects, and cars, and reduce the costs of correcting and repairing future
damage.
Visibility In the atmosphere, sulfur dioxide and nitrogen oxides form sulfate and nitrate particles, which impair visibility and affect the enjoyment of national parks and other scenic views. Extend the distance and increase the clarity at which scenery can be viewed, thus reducing limited and hazy scenes and increasing the enjoyment of national parks and other vistas.
degree of damage depends on several factors, one of which is the buffering capacity of the watershed soil—the higher the alkalinity, the more slowly the lakes and streams acidify. The exposure of fish to acidified freshwater lakes and streams has been intensely studied since the 1970s. Scientists distinguish between sudden shocks and chronic (long-term) exposure to low pH levels.

Sudden, short-term shifts in pH levels result from snowmelts, which release acidic materials accumulated during the winter, or sudden rainstorms that can wash residual acid into streams and lakes. The resulting acid shock can be devastating to fish and their ecosystems. At pH levels below 4.9, fish eggs are damaged. At acid levels below 4.5, some species of fish die. Below pH 3.5, most fish die within hours. (See Table 5.2.)

TABLE 5.2

Generalized short-term effects of acidity on fish
pH range Effect
SOURCE: "Generalized Short-Term Effects of Acidity on Fish," in National Water Quality Inventory: 1998 Report to Congress, U.S. Environmental Protection Agency, June 2000
6.5–9 No effect
6.0–6.4 Unlikely to be harmful except when carbon dioxide levels are very high (1,000 mg l-1)
5.0–5.9 Not especially harmful except when carbon dioxide levels are high (20 mg I1) or ferric ions are present
4.5–4.9 Harmful to the eggs of salmon and trout species (salmonids) and to adult fish when levels of Ca2, Na+and Cl-are low
4.0–4.4 Harmful to adult fish of many types which have not been progressively acclimated to low pH
3.5–3.9 Lethal to salmonids, although acclimated roach can survive for longer
3.0–3.4 Most fish are killed within hours at these levels
Because many species of fish hatch in the spring, even mild increases in acidity can harm or kill the new life. Temporary increases in acidity also affect insects and other invertebrates, such as snails and crayfish, on which the fish feed.

Gradual decreases of pH levels over time affect fish reproduction and spawning. Moderate levels of acidity in water can confuse a salmon's sense of smell, which it uses to find the stream from which it came. Atlantic salmon are unable to find their home streams and rivers because of acid rain. In addition, excessive acid levels in female fish cause low amounts of calcium, thereby preventing the production of eggs. Even if eggs are produced, their development is often abnormal.

Increased acidity can also cause the release of aluminum and manganese particles that are stored in a lake or river bottom. High concentrations of these metals are toxic to fish.

Soil and Vegetation
Acid rain is believed to harm vegetation by changing soil chemistry. Soils exposed to acid rain can gradually lose valuable nutrients, such as calcium, magnesium, and potassium and become too concentrated with dissolved inorganic aluminum, which is toxic to vegetation. Long-term changes in soil chemistry may have already affected sensitive soils, particularly in forests. Forest soils saturated in nitrogen cannot retain other nutrients required for healthy vegetation. Subsequently, these nutrients are washed away. Nutrient-poor trees are more vulnerable to climatic extremes, pest invasion, and the effects of other air pollutants, such as ozone.

FIGURE 5.4

Some researchers believe that acid rain disrupts soil regeneration, which is the recycling of chemical and mineral nutrients through plants and animals back to the Earth. They also believe acids suppress decay of organic matter, a natural process needed to enrich the soils. Valuable nutrients such as calcium and magnesium are normally bound to soil particles and are, therefore, protected from being rapidly washed into groundwater. Acid rain, however, may accelerate the process of breaking these bonds to rob the soil of these nutrients. This, in turn, decreases plant uptake of vital nutrients. (See Figure 5.4.)

Acid deposition can cause leafy plants such as lettuce to hold increased amounts of potentially toxic substances such as the mineral cadmium. Research also finds a decrease in carbohydrate production in the photosynthesis process of some plants exposed to acid conditions. Research is under way to determine whether acid rain could ultimately lead to a permanent reduction in tree growth, food crop production, and soil quality. Effects on soils, forests, and crops are difficult to measure because of the many species of plants and animals, the slow rate at which ecological changes occur, and the complex interrelationships between plants and their environment.

trees
trees. The effect of acid rain on trees is influenced by many factors. Some trees adapt to environmental stress better than others; the type of tree, its height, and its leaf structure (deciduous or evergreen) influence how well it will adapt to acid rain. Scientists believe that acid rain directly harms trees by leaching calcium from their foliage and indirectly harms them by lowering their tolerance to other stresses.

According to the EPA, acid rain has also been implicated in impairing the winter hardening process of some trees, making them more susceptible to cold-weather damage. In some trees the roots are prone to damage because the movement of acidic rain through the soil releases aluminum ions, which are toxic to plants.

One area in which acid rain has been linked to direct effects on trees is from moist deposition via acidic fogs and clouds. The concentrations of acid and SOx in fog droplets are much greater than in rainfall. In areas of frequent fog, such as London, significant damage has occurred to trees and other vegetation because the fog condenses directly on the leaves.

Birds
Increased freshwater acidity harms some species of migratory birds. Experts believe the dramatic decline of the North American black duck population since the 1950s is because of decreased food supplies in acidified wetlands. Acid rain leaches calcium out of the soil and robs snails of the calcium they need to form shells. Because titmice and other species of songbirds get most of their calcium from the shells of snails, the birds are also perishing. The eggs they lay are defective—thin and fragile. The chicks either do not hatch or have bone malformations and die.

In "Adverse Effects of Acid Rain on the Distribution of the Wood Thrush Hylocichla mustelina in North America" (Proceedings of the National Academy of Sciences, August 12, 2002), Ralph S. Hames et al. discuss the results of their large-scale study, which shows a clear link between acid rain and widespread population declines in the wood thrush, a type of songbird. Hames and his colleagues believe that calcium depletion has had a negative impact on this bird's food source, mainly snails, earthworms, and centipedes. The bird may also be ingesting high levels of metals that are more likely to leach out of overly acidic soils. Declining wood thrush populations are most pronounced in the higher elevations of the Adirondack, Great Smoky, and Appalachian mountains. Hames and his cohorts warn that acid rain may also be contributing to population declines in other songbird species.

Materials
Acid rain can also be harmful to materials, such as building stones, marble statues, metals, and paints. Elaine McGee of the U.S. Geological Service reports in Acid Rain and Our Nation's Capital (1997, http://pubs.usgs.gov/gip/acidrain/contents.html) that limestone and marble are particularly vulnerable to acid rain. Historical monuments and buildings composed of these materials in the eastern United States have been hit hard by acid rain.

Human Health
Acid rain has several direct and indirect effects on humans. Particulates are extremely small pollutant particles that can threaten human health. Particulates related to acid rain include fine particles of SOx and nitrates. These particles can travel long distances and, when inhaled, penetrate deep into the lungs. Acid rain and the pollutants that cause it can lead to the development of bronchitis and asthma in children. Acid rain is also believed to be responsible for increasing health risks for those over the age of sixty-five; those with asthma, chronic bronchitis, and emphysema; pregnant women; and those with histories of heart disease.

THE POLITICS OF ACID RAIN
Scientific research on acid rain was sporadic and largely focused on local problems until the late 1960s, when Scandinavian scientists began more systematic studies. Acid precipitation in North America was not identified until 1972, when scientists found that precipitation was acidic in eastern North America, especially in northeastern and eastern Canada. In 1975 the First International Symposium on Acid Precipitation and the Forest Ecosystem convened in Columbus, Ohio, to define the acid rain problem. Scientists used the meeting to propose a precipitation-monitoring network in the United States that would cooperate with the European and Scandinavian networks and to set up protocols for collecting and testing precipitation.

In 1977 the Council on Environmental Quality was asked to develop a national acid rain research program. Several scientists drafted a report that eventually became the basis for the National Acid Precipitation Assessment Program (NAPAP). This initiative eventually translated into legislative action with the Energy Security Act of 1980. Title VII (Acid Precipitation Act of 1980) of the act produced a formal proposal that created NAPAP and authorized federally financed support.

The first international treaty aimed at limiting air pollution was the United Nations Economic Commission for Europe (UNECE) Convention on Long-Range Trans-boundary Air Pollution, which went into effect in 1983. It was ratified by thirty-eight of the fifty-four UNECE members, which included not only European countries but also Canada and the United States. The treaty targeted sulfur emissions, requiring that countries reduce emissions 30% from 1980 levels—the so-called Thirty Percent Club.

The early acid rain debate centered almost exclusively on the eastern United States and Canada. The controversy was often defined as a problem of property rights. The highly valued production of electricity in coal-fired utilities in the Ohio River Valley caused acid rain to fall on land in the Northeast and Canada. An important part of the acid rain controversy in the 1980s was the adversarial relationship between U.S. and Canadian government officials over emission controls of SO2 and NO2. More of these pollutants crossed the border into Canada than the reverse. Canadian officials very quickly came to a consensus over the need for more stringent controls, whereas this consensus was lacking in the United States.

Throughout the 1980s the major lawsuits involving acid rain all came from eastern states, and the states that passed their own acid rain legislation were those in the eastern part of the United States.

Legislative attempts to restrict emissions of pollutants were often defeated after strong lobbying by the coal industry and utility companies. These industries advocated further research for pollution-control technology rather than placing restrictions on utility company emissions.

The NAPAP Controversy
In 1980 Congress established NAPAP to study the causes and effects of acid deposition and recommend policy approaches for controlling acid rain effects. About two thousand scientists worked on this unique inter-agency program, which ultimately cost more than $500 million. Even though its first report was due in 1985, the program was plagued by problems that resulted in numerous delays. In 1985 the first executive director, Christopher Bernabo, resigned and was replaced by Lawrence Kulp. In 1987 the study group released to Congress Interim Assessment: The Causes and Effects of Acidic Deposition, a massive four-volume preliminary report that caused a storm of controversy. The report contained detailed scientific information in its technical chapters about acid rain. The executive summary, written by Kulp, was released to the public and widely criticized for mis-representing the scientific findings of the report and downplaying the negative effects of acid rain. Philip Shabecoff notes in "Acid Rain Report Unleashes a Torrent of Controversy" (New York Times, March 20, 1990) that critics claimed Kulp had slanted the summary to match the political agenda of the administration of President Ronald Reagan (1911–2004), which advocated minimum regulation of business and industry.

Some of the scientific findings in the 1987 report included:

Acid rain had adversely affected aquatic life in about 10% of eastern lakes and streams.
Acid rain had contributed to the decline of red spruce at high elevations by reducing this species' cold tolerance.
Acid rain had contributed to erosion and corrosion of buildings and materials.
Acid rain and related pollutants had reduced visibility throughout the Northeast and in parts of the West.
The report concluded, however, that the incidence of serious acidification was more limited than originally feared. At that time the Adirondacks area of New York was the only region showing widespread, significant damage from acid. Furthermore, results indicated that electricity-generating power plants were responsible for two-thirds of SO2 emissions and one-third of NOx emissions.

Controversy over Kulp's role led to him being replaced by James Mulhoney. The new director ordered reassessments and revisions of the interim report. This was completed in 1991. However, by that time President George H. W. Bush (1924–) was in power, and he had made acid rain legislation a component of his election campaign. As a result, political forces, rather than NAPAP, largely drove the nation's emerging policy toward acid rain.

THE ACID RAIN PROGRAM—CLEAN AIR ACT AMENDMENTS, TITLE IV
Congress created the Acid Rain Program under Title IV (Acid Deposition Control) of the 1990 Clean Air Act Amendments. The goal of the program is to reduce annual emissions of SO2 and NOx from electric power plants nationwide. The program set a permanent cap on the total amount of SO2 that could be emitted by these power plants. According to the EPA, in Acid Rain Program: 2005 Progress Report (October 2006, http://www.epa.gov/airmarkets/progress/docs/2005report.pdf), this cap was set at 8.9 million tons (approximately half the number of tons of SO2 emitted by these plants during 1980). The program also established NOx emissions limitations for certain coal-fired electric utility plants. The objective of these limitations was to achieve and maintain a two-million-ton reduction in NOx emission levels by 2000 compared with the emissions that would have occurred in 2000 if the limitations had not been implemented.

In the 1999 Compliance Report: Acid Rain Program (July 2000, http://www.epa.gov/airmarkets/progress/docs/1999compreport.pdf), the EPA indicates that the reduction was implemented in two phases. Phase I began in 1995 and covered 263 units at 110 utility plants in 21 states with the highest levels of emissions. Most of these units were at coal-burning plants located in eastern and midwestern states. They were mandated to reduce their annual SO2 emissions by 3.5 million tons. An additional 182 units joined Phase I voluntarily, bringing the total of Phase I units to 445.

Phase II began in 2000. It tightened annual emission limits on the Phase I group and set new limits for more than two thousand cleaner and smaller units in all forty-eight contiguous states and the District of Columbia.

A New Flexibility in Meeting Regulations
Traditionally, environmental regulation has been achieved by the "command and control" approach, in which the regulator specifies how to reduce pollution, by what amount, and what technology to use. Title IV, however, gave utilities flexibility in choosing how to achieve these reductions. For example, utilities could reduce emissions by switching to low-sulfur coal, installing pollution-control devices called scrubbers, or shutting down plants.

Utilities took advantage of their flexibility under Title IV to choose less costly ways to reduce emissions—many switching from high- to low-sulfur coal—and as a result, they have been achieving sizable reductions in their SO2 emissions.

Allowance Trading
Title IV also allows electric utilities to trade allowances to emit SO2. Utilities that reduce their emissions below the required levels can sell their extra allowances to other utilities to help them meet their requirements.

Title IV allows companies to buy, sell, trade, and bank pollution rights. Utility units are allocated allowances based on their historic fuel consumption and a specific emissions rate. Each allowance permits a unit to emit one ton of SO2 during or after a specific year. For each ton of SO2 discharged in a given year, one allowance is retired and can no longer be used. Companies that pollute less than the set standards will have allowances left over. They can then sell the difference to companies that pollute more than they are allowed, bringing them into compliance with overall standards. Companies that clean up their pollution would recover some of their costs by selling their pollution rights to other companies.

The EPA holds an allowance auction each year. The sale offers allowances at a fixed price. This use of market-based incentives under Title IV is regarded by many as a major new method for controlling pollution.

From 1995 to 1998 there was considerable buying and selling of allowances among utilities. Because the utilities that participated in Phase I reduced their sulfur emissions more than the minimum required, they did not use as many allowances as they were allocated for the first four years of the program. Those unused allowances could be used to offset SO2 emissions in future years. In Acid Rain: Emissions Trends and Effects in the Eastern United States (March 2000, http://www.gao.gov/archive/2000/rc00047.pdf), the U.S. General Accounting Office (now the U.S. Government Accountability Office) notes that from 1995 to 1998 a total of 30.2 million allowances were allocated to utilities nationwide; almost 8.7 million,

FIGURE 5.5

or 29%, of the allowances were not used but were carried over (banked) for subsequent years.

Figure 5.5 shows the status of the allowance bank from 1995 through 2005. Banked allowances increased dramatically in 2000 due to the addition of the Phase II sources to the Acid Rain Program. Over the next five years the allowance bank steadily decreased in size. The EPA reports in Acid Rain Program: 2005 Progress Report that in 2005 a total of 9.5 million allowances were allocated. Another 6.9 million banked allowances were carried over from previous years. The EPA expects that the allowance bank will eventually be depleted as SO2 emissions are further restricted by the implementation of the Clean Air Interstate Rule.

PERFORMANCE RESULTS OF THE ACID RAIN PROGRAM
There are three quantitative measures that environmental regulators use to gauge the performance of the Acid Rain Program: emissions, atmospheric concentrations, and deposition amounts.

U.S. Progress Report
The following information comes from the EPA's Acid Rain Program: 2005 Progress Report.

sources and emissions
sources and emissions. The report notes that in 2005 there were 3,456 electric generating units subject to the SO2 provisions of the Acid Rain Program. Most emissions were associated with approximately 1,100 coal-fired units making up the total. In all, program sources emitted 10.2 million tons of SO2 into the air. (See Figure 5.6.) The EPA expects that the 8.9-million-ton annual cap on emissions will be achieved by 2010. SO2 emissions from sources covered by the program decreased by 41% between 1980 and 2005.

In 2005 the NOx portion of the Acid Rain Program applied to a subset of the 3,456 units mentioned earlier, specifically 982 operating coal-fired units generating at least 25 megawatts. Between 1990 and 2005 NOx emissions from power plants subject to the Acid Rain Program decreased from 5.5 million tons per year to 3.3 million tons per year. (See Figure 5.7.)

According to the report, in 2000 the program first achieved its goal of reducing emissions by at least 2 million tons; 8.1 million tons were originally predicted in 1990 to be emitted in 2000 without the program in place.

The report indicates that the SO2 and NOx emission reductions were achieved even though the amount of fuel used to produce electricity in the United States increased by more than 30% between 1990 and 2005. Coal was the

FIGURE 5.6

FIGURE 5.7

single-largest fuel source for U.S. electric generating plants in 2005, accounting for 50% of the total.

atmospheric concentrations and deposition amounts
atmospheric concentrations and deposition amounts. The EPA's Acid Rain Program uses two complementary monitoring networks to track trends in regional air quality and acid deposition: the Clean Air Status and Trends Network and the NADP's National Trends Network. Additional monitoring data are provided by national, state, and local ambient monitoring systems.

As shown in Figure 2.14 and Figure 2.6 in Chapter 2, atmospheric levels of SO2 and NO2 averaged nationwide since 1990 have been well below the national standards for these pollutants.

Table 5.3 shows trends in atmospheric concentrations and deposition for four key regions in the Acid Rain Program: mid-Atlantic, Midwest, Northeast, and Southeast. Overall, concentrations of ambient SO2 and wet sulfates averaged over the period 2003–05 declined in all these regions, compared with the period 1989–91. The most dramatic differences are evident in the Northeast, where ambient SO2 concentrations decreased by more than 50%. The results for nitrogen and nitrate compound concentrations are mixed, with decreases in some areas and increases in others. The same is true for wet inorganic nitrogen deposition, which decreased in the mid-Atlantic, Midwest, and Northeast, but increased slightly in the Southeast.

Canadian Progress Report
In November 2006 Environment Canada released a report on progress made by Canada and the United States on cross-border air pollution. The study, Canada–United States Air Quality Agreement: 2006 Progress Report (http://www.ec.gc.ca/cleanair-airpur/caol/canus/report/2006canus/toc_e.cfm), is the eighth biennial report related to the 1991 agreement between the two countries. The report states that Canada has been successful at reducing SO2 emissions below its national cap. Canada's total SO2 emissions were 2.3 million tonnes (metric tons) in 2004, which is 28% below the national cap of 3.2 million tonnes. However, Environment Canada notes that the reductions have not been sufficient to reduce acid deposition below the levels needed to ensure the recovery of ecosystems damaged by excess acidity in its eastern provinces.

ARE ECOSYSTEMS RECOVERING?
Monitoring data clearly indicate decreased emissions and atmospheric concentrations of SO2 and NOx and some reductions in deposition amounts. These improvements have not necessarily resulted in recovery of sensitive aquatic and terrestrial ecosystems. This is due, in part, to the long recovery times required to reverse damage done by acidification. The EPA reports that ecosystems

TABLE 5.3

Regional changes in air quality and deposition of sulfur and nitrogen, 1989–91 and 2003–05
Average
Measurement Unit Region 1989–1991 2003–2005 Percent change*
SOURCE: "Table 4. Regional Changes in Air Quality and Deposition of Sulfur and Nitrogen, 1989–1991 Versus 2003–2005," in Acid Rain Program: 2005 Progress Report, U.S. Environmental Protection Agency, October 2006, http://www.epa.gov/airmarkets/progress/docs/2005report.pdf (accessed June 19, 2007)
*Percent change is estimated from raw measurement data, not rounded; some of the measurement data used to calculate percentages may be at or below detection limits.
Notes: kg=kilogram. ha=hectare. mg=milligram. L=liter. µg=microgram. m3=cubic meter.
Wet sulfate deposition kg/ha Mid-Atlantic 27 20 -24
Wet sulfate concentration mg/L Mid-Atlantic 2.4 1.6 -33
Midwest 2.3 1.6 -30
Northeast 1.9 1.1 -40
Southeast 1.3 1.1 -21
Ambient sulfur dioxide concentration µg/m3 Mid-Atlantic 13 8.4 -34
Midwest 10 5.8 -44
Northeast 6.8 3.1 -54
Southeast 5.2 3.4 -35
Ambient sulfate concentration µg/m3 Mid-Atlantic 6.4 4.5 -30
Midwest 5.6 3.8 -33
Northeast 3.9 2.5 -36
Southeast 5.4 4.1 -24
Wet inorganic nitrogen deposition kg/ha Mid-Atlantic 5.9 5.5 -8
Midwest 6.0 5.5 -8
Northeast 5.3 4.1 -23
Southeast 4.3 4.4 +2
Wet nitrate concentration mg/L Mid-Atlantic 1.5 1.0 -29
Midwest 1.4 1.2 -14
Northeast 1.3 0.9 -33
Southeast 0.8 0.7 -9
Ambient nitrate concentration µg/m3 Mid-Atlantic 0.9 1.0 +5
Midwest 2.1 1.8 -14
Northeast 0.4 0.5 +20
Southeast 0.6 0.7 +17
Total ambient nitrate concentration (nitrate + nitric acid) µg/m3 Mid-Atlantic 3.5 3.0 -14
Midwest 4.0 3.5 -12
Northeast 2.0 1.7 -13
Southeast 2.2 2.1 -5
harmed by acid rain deposition can take a long time to fully recover even after harmful emissions cease. The most chronic aquatic problems can take years to be resolved. Forest health is even slower to improve following decreases in emissions, taking decades to recover. Finally, soil nutrient reserves (such as calcium) can take centuries to replenish.

The most recent comprehensive analysis of acidified ecosystems was presented by NAPAP in the National Acid Precipitation Assessment Program Report to Congress: An Integrated Assessment (2003, http://www.cleartheair.org/documents/NAPAP_FINAL_print.pdf). The report presents a literature review summarizing findings from various government and academic studies. Overall, NAPAP finds that some ecosystems affected by acid deposition are showing limited signs of recovery. For example, one study shows that more than 25% of affected lakes and streams studied in the Adirondacks and northern Appalachians are no longer acidic. However, little to no improvement has been seen in examined water bodies in other regions, including New England and portions of Virginia. The report notes that even though chemical recovery has begun in some waterways, complete recovery for aquatic life forms, such as fish, is expected to take "significantly longer."

In regards to terrestrial ecosystems, NAPAP reports that forests are under many stresses besides acid rain, such as global warming, land use changes, and air pollution from urban, agricultural, and industrial sources. The combined effect of these stressors has greatly limited forest recovery from acidification. According to NAPAP, "There are as yet no forests in the U.S. where research indicates recovery from acid deposition is occurring." However, it is expected that reduced emissions under the Acid Rain Program will benefit forests in the long term.

The report acknowledges the future benefits of continued implementation of the Acid Rain Program, but it concludes that "the emission reductions achieved by Title IV are not sufficient to allow recovery of acid-sensitive ecosystems." Recent studies support the idea that additional emission cuts 40% to 80% beyond those of the existing program will be needed to protect acid-sensitive ecosystems. NAPAP modeling indicates that even virtual elimination of SO2 emissions from power plants will be insufficient to provide this protection. It is believed that emission reductions from other sources (such as the industrial and transport sectors) will be necessary.

The Next Step: The Clean Air Interstate Rule
In 2005 the EPA issued the Clean Air Interstate Rule (CAIR; April 5, 2007, http://www.epa.gov/cair/) to address the transport of air pollutants across state lines in the eastern United States. CAIR puts permanent caps on emissions of SO2 and NOx in twenty-eight eastern states and the District of Columbia. It is expected to reduce SO2 emissions by more than 70% and reduce NOx emissions by more than 60% compared with 2003 levels. These measures should reduce the formation of acid rain and other pollutants, such as fine particulate matter and ground-level ozone.

The CAIR program will use a cap-and-trade system similar to that used in the SO2 portion of the acid rain program. The EPA projects that complete implementation of CAIR in 2015 will result in up to $100 billion in annual health benefits and a substantial reduction in premature deaths because of air pollution in the eastern United States. It should also improve visibility in southeastern national parks that have been plagued by smog in recent years.

PUBLIC OPINION ABOUT ACID RAIN
Every year the Gallup Organization polls Americans about their attitudes regarding environmental issues. The most recent poll to assess acid rain was conducted in March 2007. Participants were asked to express their level of personal concern about various environmental issues, including acid rain, water pollution, soil contamination, air pollution, plant and animal extinctions, loss of tropical rain forests, damage to the ozone layer, and global warming. The results showed that acid rain ranked last among these environmental problems.

Analysis of historical Gallup poll results shows a dramatic decline in concern about acid rain since the late 1980s. (See Table 5.4.) In 1989 Gallup found that 41% of respondents felt a great deal of concern about acid rain and 11% felt none at all. By 2007 only 25% of people polled were concerned a great deal about acid rain and 20% expressed no concern about the acid rain issue.

TABLE 5.4

Public concern about acid rain, 1989–2007
Great deal Fair amount Only a little Not at all No opinion
SOURCE: "I'm going to read you a list of environmental problems. As I read each one, please tell me if you personally worry about this problem a great deal, a fair amount, only a little, or not at all. First, how much do you personally worry about—Acid Rain," in Environment, The Gallup Organization, 2007, http://www.galluppoll.com/content/?ci=1615&pg=1 (accessed June 19, 2007). Copyright © 2007 by The Gallup Organization. Reproduced by permission of The Gallup Organization.

Quantum Theory

quantum theory

quantum theory, modern physical theory concerned with the emission and absorption of energy by matter and with the motion of material particles; the quantum theory and the theory of relativity together form the theoretical basis of modern physics. Just as the theory of relativity assumes importance in the special situation where very large speeds are involved, so the quantum theory is necessary for the special situation where very small quantities are involved, i.e., on the scale of molecules, atoms, and elementary particles. Aspects of the quantum theory have provoked vigorous philosophical debates concerning, for example, the uncertainty principle and the statistical nature of all the predictions of the theory.

Relationship of Energy and Matter

According to the older theories of classical physics, energy is treated solely as a continuous phenomenon, while matter is assumed to occupy a very specific region of space and to move in a continuous manner. According to the quantum theory, energy is held to be emitted and absorbed in tiny, discrete amounts. An individual bundle or packet of energy, called a quantum (pl. quanta), thus behaves in some situations much like particles of matter; particles are found to exhibit certain wavelike properties when in motion and are no longer viewed as localized in a given region but rather as spread out to some degree.


For example, the light or other radiation given off or absorbed by an atom has only certain frequencies (or wavelengths), as can be seen from the line spectrum associated with the chemical element represented by that atom. The quantum theory shows that those frequencies correspond to definite energies of the light quanta, or photons, and result from the fact that the electrons of the atom can have only certain allowed energy values, or levels; when an electron changes from one allowed level to another, a quantum of energy is emitted or absorbed whose frequency is directly proportional to the energy difference between the two levels.

Dual Nature of Waves and Particles

The restriction of the energy levels of the electrons is explained in terms of the wavelike properties of their motions: electrons occupy only those orbits for which their associated wave is a standing wave (i.e., the circumference of the orbit is exactly equal to a whole number of wavelengths) and thus can have only those energies that correspond to such orbits. Moreover, the electrons are no longer thought of as being at a particular point in the orbit but rather as being spread out over the entire orbit. Just as the results of relativity approximate those of Newtonian physics when ordinary speeds are involved, the results of the quantum theory agree with those of classical physics when very large "quantum numbers" are involved, i.e., on the ordinary large scale of events; this agreement in the classical limit is required by the correspondence principle of Niels Bohr. The quantum theory thus proposes a dual nature for both waves and particles, one aspect predominating in some situations, the other predominating in other situations.

Evolution of Quantum Theory

Early Developments

While the theory of relativity was largely the work of one man, Albert Einstein, the quantum theory was developed principally over a period of thirty years through the efforts of many scientists. The first contribution was the explanation of blackbody radiation in 1900 by Max Planck, who proposed that the energies of any harmonic oscillator (see harmonic motion), such as the atoms of a blackbody radiator, are restricted to certain values, each of which is an integral (whole number) multiple of a basic, minimum value. The energy E of this basic quantum is directly proportional to the frequency ? of the oscillator, or E=h?, where h is a constant, now called Planck's constant, having the value 6.63×10-34 joule-second. In 1905, Einstein proposed that the radiation itself is also quantized according to this same formula, and he used the new theory to explain the photoelectric effect. Following the discovery of the nuclear atom by Rutherford (1911), Bohr used the quantum theory in 1913 to explain both atomic structure and atomic spectra, showing the connection between the electrons' energy levels and the frequencies of light given off and absorbed.

Quantum Mechanics and Later Developments

Quantum mechanics, the final mathematical formulation of the quantum theory, was developed during the 1920s. In 1924, Louis de Broglie proposed that not only do light waves sometimes exhibit particlelike properties, as in the photoelectric effect and atomic spectra, but particles may also exhibit wavelike properties. This hypothesis was confirmed experimentally in 1927 by C. J. Davisson and L. H. Germer, who observed diffraction of a beam of electrons analogous to the diffraction of a beam of light. Two different formulations of quantum mechanics were presented following de Broglie's suggestion. The wave mechanics of Erwin Schrödinger (1926) involves the use of a mathematical entity, the wave function, which is related to the probability of finding a particle at a given point in space. The matrix mechanics of Werner Heisenberg (1925) makes no mention of wave functions or similar concepts but was shown to be mathematically equivalent to Schrödinger's theory.

Quantum mechanics was combined with the theory of relativity in the formulation of P. A. M. Dirac (1928), which, in addition, predicted the existence of antiparticles. A particularly important discovery of the quantum theory is the uncertainty principle, enunciated by Heisenberg in 1927, which places an absolute theoretical limit on the accuracy of certain measurements; as a result, the assumption by earlier scientists that the physical state of a system could be measured exactly and used to predict future states had to be abandoned. Other developments of the theory include quantum statistics, presented in one form by Einstein and S. N. Bose (the Bose-Einstein statistics) and in another by Dirac and Enrico Fermi (the Fermi-Dirac statistics); quantum electrodynamics, concerned with interactions between charged particles and electromagnetic fields; its generalization, quantum field theory; and quantum electronics.