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ABOUT THE BOOK

The current status of reactive nitrogen which consists of all biologically, chemically and radiatively active nitrogen
compounds in terrestrial, coastal and atmospheric realms and development of technologies to minimize nitrogen In Agriculture, Industry and Environment in India
impacts on the environment needs to be addressed in the right perspective. The development of policy to control
unwanted reactive N release in the environment is difficult because much of the reactive N release is related
to food and energy production and reactive N species can be transported great distances in the atmosphere
• Bijay Singh • Mithilesh K. Tiwari • Yash P. Abrol
and in aquatic systems.
This publication is an outcome of the activities of the Indian Nitrogen Group, a national network of scientists
concerned with issues related to reactive nitrogen. It presents an overview of reactive nitrogen in agriculture,
industry and environment in India. Since reliable quantitative information about several aspects of reactive
nitrogen in the country is not yet available, it should prove very valuable for the scientific community in terms
of initiating projects to fill the gaps. It should also help planners in agriculture, industry and energy production
to guide future expansion in the economy in a way that the delicate balance between inputs and outputs of
reactive nitrogen in the environment is maintained.

ABOUT THE AUTHORS


Professor Bijay Singh, ICAR Dr. Mithilesh K. Tiwari is Director of Professor Yash P Abrol, formerly Head
National Professor, has been working the South Asian Regional Centre of the of the Division of Plant Physiology at
on different aspects of nitrogen in International START Programme that is the Indian Agricultural Research Precipitation

rice-wheat cropping system for more responsible for nurturing regional Institute, New Delhi, subsequent to
than two decades. His contributions cooperation for studies on Global serving as CSIR Emeritus Scientist and Gaseous Losses

Organic Residues
on nitrogen balance in soil-plant Change with particular emphasis now INSA Senior Scientist (1996-2001; 2001- Denitrification
Plant Consumption
Organic Matter

systems have lead to better on Climate Change Adaptation. He 2005), is at present associated with the Nitrates Nitrification
Mineralization
Ammonium
through bacteria

heads the Centre on Global Change Department of Environmental Botany, Fixation

understanding for (i) enhancing Leaching Nitrites Clay Minerals

Project of CSIR and the Radio and Hamdard University, New Delhi as
nitrogen use efficiency in rice-wheat
Adjunct Professor and INSA Honorary Jammu & Seagull
cropping system (ii) fertilizer nitrogen Atmospheric Sciences Division, Kashmir Atmospheric N2

Scientist,. He has immensely contributed Himachal


related environmental pollution, and National Physical Laboratory at New Pradesh
Wetland
to nitrogen research and has published Punjab Uttaranchal Vegetation
(iii) integrated nutrient management. Delhi. He is an active Core Team DELHI
Arunachal
Pradesh Oceans
profusely in reputed journals. He is Uttar
Sikkim
Assam
containing
CO(NH2)2
He is a fellow of Indian National Member of the Indian Nitrogen Group. actively involved in organizing INDIAN
Rajasthan Pradesh
Bihar Megalaya
Nagaland
Manipur
Tripura
He has extensively contributed to the

Jh a
Science Academy, National Academy Gujarat West Mizoram

r kh
NITROGEN GROUP under the aegis of Madhya Pradesh Bengal

and
rh
ga Decaying
of Agricultural Sciences and Indian growth of several major national level the Society for Conservation of Nature. Ch
ttis
ha Orissa
Kolkata
(Calcutta) Nitrogen fixing
dead animal
Mumbai Maharashtra soil bacteria
Society of Soil Science. He is decorated research programmes in space sciences. He is a Fellow of the INSA, Indian
(Bombay) Denitrification
by denitrifying
bacteria
Andhra

with several awards notably the Rafi His research interests are atmospheric Academy of Sciences, National Academy Goa a tak
a Pradesh
Ammonification
Decomposition
(Bacteria and
K ar n fungi)

Ahmad Kidwai Memorial Prize of environmental change processes and of Sciences and NAAS. He received Lakshdeep Chennai (Madras)
(NH4+) Ammonium (NH4+)
Open Water

ICAR. He is continuing work on impacts. Currently member of INSA’s several awards notably ICAR National Tamil
Kerala Nadu
Andaman & Nicobar
Assimilation
Nitrification by
nitrifying
Nitrification by
nitrifying bacteria
Nitrogen bacteria

increasing fertilizer nitrogen use National Committee for SCAR, he also Fellowship, FAI Dhirubhai Morarji (NO2) Nitrites
(NO2)

efficiency in rice and wheat at Punjab served the National Committees for IGBP Memorial, R.D. Asana, Sukumar Basu,
Agricultural University, Ludhiana. and COSPAR. VASVIK and FICCI awards.

INDIAN NATIONAL SCIENCE ACADEMY


Bahadur Shah Zafar Marg, New Delhi-110002
i

Reactive Nitrogen in Agriculture,


Industry and Environment in India

Bijay Singh
M.K. Tiwari
and
Y.P. Abrol

INDIAN NATIONAL SCIENCE ACADEMY


Bahadur Shah Zafar Marg, New Delhi-110002
© Indian National Science Academy
Bahadur Shah Zafar Marg, New Delhi-110002

EPABX Nos.: 23221931-23221950 (20 lines)


Fax : 91-11-23231095, 23235648
E-mail : council@insa.nic.in; esoffice@insa.nic.in
Website : http://www.insaindia.org

Published by Shri SK Sahni, Executive Secretary on behalf of Indian National Science Academy, Bahadur Shah Zafar marg, New Delhi-110002
and printed at Aakriti Graphics, New Delhi.
Reactive Nitrogen in Agriculture, Industry and Environment in India iii

Foreword

The Indian National Science Academy (INSA), New Delhi, is the adhering body in India to the International
Council for Science (ICSU) and its affiliated International Unions / Committees / Commissions, etc. A
joint National Committee of IGBP-WCRP-SCOPE, formed by INSA, looks after and supports the activities
and implementation of various projects in these areas. The Committee decided that a series of status
reports be prepared on specific topics by leading Indian experts so that Indian work be highlighted at
various general awareness be created among scientists and science students.
Recent assessments of the state of the environment across India indicate that the country’s rising
economic prosperity is also putting the environment under stress. Human food and energy production
has dramatically increased the amount of atmospheric N2 that is converted into reactive forms. As a
consequence there is a wide variety of beneficial and detrimental effects. Reactive nitrogen is thus associated
with both growing economy in terms of food production and industry, and environmental degradation.
Burgeoning human population depends upon food production made possible by synthetic nitrogen
fertilizers. Combustion of fossil fuels adds more reactive nitrogen to air, water and soil. This distortion
of the nitrogen cycle, while raising agricultural yields, causes degradation of water and air quality,
biodiversity, ecosystem services and human health. Meanwhile, reactive nitrogen deficiencies on farmland
in many regions of the country continue to create economic and health hardships, and accelerate land
degradation. The development of policy to control unwanted reactive N release in the environment is
difficult because much of the reactive N release is related to food and energy production and reactive
N species can be transported great distances in the atmosphere and in aquatic systems. Although the
nitrogen cycle provides a framework for assessing broad scale or even global strategies to improve nitrogen
use efficiency, nitrogen cycling occurs at region scale and policies can be implemented and enforced at
the national or provincial/state levels. Multinational efforts to control N loss to the environment are surely
needed, but these efforts will require commitments from individual countries and the policy-makers within
those countries.
The present booklet dealing with ‘Reactive Nitrogen in Agriculture, Industry and Environment in
India’ is the third in the IGBP-WCRP-SCOPE series, and presents an overview of reactive nitrogen in
agriculture, industry and environment in India. The information compiled by the authors should help
planners in agriculture, industry and energy production to guide future expansion in the economy in a
way that the delicate balance between inputs and outputs of reactive nitrogen in the environment is
maintained.

Date: January, 2008 M Vijayan


Place: New Delhi President
Indian National Science Academy
4 Bijay Singh, MK Tiwari and YP Abrol

BLANK
Reactive Nitrogen in Agriculture, Industry and Environment in India v
5

Fax: (0542) 2368174 Phones: (Off) (0542) 2368399


E-mail: singh.js1@gmail.com (Res) (0542) 2369093
jssingh@bhu.ac.in (Mob) +91 9335178355

BANARAS HINDU UNIVERSITY


Ecosystems Analysis Laboratory

J.S. SINGH PhD FTWAS FNA FASc FNASc DEPARTMENT OF BOTANY


VARANASI-221005, INDIA

Preface
While majority of the Indian agricultural soils are deficient in usable forms of nitrogen, uneven/excessive/
improper/inappropriate use of N fertilizers, coupled with contributions from industrial effluents/exhausts,
animal wastes and geo-deposits have led to widespread pollution of groundwater and eutrophication of
surface waters posing a severe problem for public health and the ecosystem. The ozone-depleting and
greenhouse effects of NOx gases from various farm and non-farm sources may pose new concerns for
nitrogen-carbon balance. There is no escape from the use of fertilizers to sustain food production, and
the environmental consequences of accumulation of reactive N are the same, regardless of whether the
fertilizers are of chemical or biological origin. Therefore, the challenge now facing Indian agriculture is
to further enhance the productivity of our agricultural system without adversely impacting our environment
and ecology. This necessitates an integrated understanding of nitrogen in India’s agriculture, industry and
environment so as to identify the appropriate sites for intervention towards a more sustainable N
management regime.

At the request of the IGBP-WCRP-SCOPE National Committee, Professor Y.P. Abrol a pioneer researcher
in the area of reactive nitrogen and Fellow of the Indian National Science Academy, agreed to distill the
current thinking in India with regard to various aspects of the nitrogen cycle with special reference to
reactive N in the lndian context, and to summarise the current knowledge as well as identify the gaps
in it for informed decisions on further research and policy. Professor Abrol chose two coauthors on the
basis of their expertise, strong and long presence in the field, and commitment to interdisciplinary
understanding on various aspects of nitrogen.

The article provides state-of-the-art review integrating global literature and India-specific information as
appropriate. I am sure the material provided here will be of use to scientists and science students interested
in SCOPE and IGBP.

J S Singh
Chairman,
IGBP-WCRP-SCOPE National Committee
6 Bijay Singh, MK Tiwari and YP Abrol

Contents

Foreword .... iii


Preface .... v
Abstract .... 1
Outline .... 1
Reactive nitrogen – definition and scope .... 2
Nitrogen fluxes, cycle and cascade effects .... 5
Nitrogen fluxes and cascade effects in India .... 5
Reactive nitrogen in Indian agriculture .... 8
Reactive nitrogen from use of fossil fuels in industry, transport and energy
production in India .... 18
Atmospheric nitric oxide (NO) and nitrous oxide (N2O) .... 22
Emission of reactive nitrogen as ammonia from terrestrial ecosystems .... 24
Nitrate-nitrogen in groundwater bodies .... 26
Nitrogen in rivers, coastal ecosystems and oceans .... 32
Challenges and options for mitigation of environmentally
important reactive nitrogen, research and planning .... 34
References .... 36
Reactive Nitrogen in Agriculture, Industry and Environment in India 1

Reactive Nitrogen in Agriculture, Industry and


Environment in India

Molecular form of nitrogen (N2) is unusable by the vast majority of living organisms. It must be transformed
or fixed into other forms collectively known as reactive nitrogen which includes all biologically, chemically
and radiatively active nitrogen compounds in the atmosphere and biosphere. The flows of reactive N in terrestrial,
aquatic and atmospheric ecosystems in India are being increasingly regulated by inputs, use efficiency and
leakages of reactive N from agriculture and growing use of fossil fuels for energy. In the last three decades,
use of reactive N in the form of chemical fertilizers has kept pace with production of food grains and at present
more than 11 Tg is being applied annually to agroecosystems in the country. As for cereal-based agriculture,
recovery of N by rice and wheat at on-farm locations in India rarely exceeds the 50% mark so that a large
portion of total N fixed biologically, applied as fertilizers or recycled as organic manures leaves agroecosystems
to reach atmosphere or aquatic realms. The greatest challenge in improving N use efficiency lies in developing
precision management of reactive N in time and space. Coal burning power plants and combustion of oil
in road transport contributed up to 33% each in total NOx emissions in India. With around 49% growth
as compared with levels in 2000, NOx emissions are estimated to be more than 7 Tg in 2020. Agricultural
activities in India account for more than 80% of the total N2O emissions – including 60% from the use of
N fertilizers and 12% from burning of agricultural residues. Application of fertilizers and the livestock in agriculture
sector are the major contributors to NH3 emissions. In Asia, reactive N transfers to the atmosphere by NH3
volatilization are expected to reach 19 Tg N year–1 in the next three decades; 29% being India’s contribution.
With very high groundwater development along with high fertilizer N use, the northwestern region in the
country has been categorized as the high risk zone for nitrate-N pollution of groundwater bodies. At several
places sources other than fertilizer N are more important for high nitrate-N levels in groundwater. Reactive
N is being exported in the form of nitrate out of watersheds of river Ganga at the rate of 601 kg
N year–1 km–2. Total reactive N in annual river runoff from South Asia amounts to more than 4 Tg. Of this
around 30 % is added to Arabian Sea adversely affecting its biogeochemical processes. Use of increasing
amounts of reactive N in the form of fertilizers in Indian agriculture and efficient management of fertilizer
N will remain at the forefront of issues to improve the reactive N balance over both the short- and long-
term. Reactive N emissions from fuel combustion (NOx) can be reduced by following strict policies but reducing
the introduction of new reactive N in food production seems to be very difficult in countries like India having
burgeoning populations. It is now technically feasible to decrease reactive N creation from fossil fuel combustion
to a point where it becomes just a minor disturbance to the reactive N cycle. Challenge ahead is to follow
the three stage strategy of the International Nitrogen Initiative in terms of assessing knowledge of N flows,
developing region specific solutions and implementing scientific, engineering and policy tools.

OUTLINE

Nitrogen is necessary for all forms of life and a crucial component in the increased production of food
to feed the continuously increasing human and animal populations. In many ecosystems on land and
sea, the supply of nitrogen controls the nature and diversity of plant life, the population dynamics of
both grazing animals and their predators, and vital ecological processes such as plant productivity and
the cycling of carbon and soil minerals. This is true not only in wild or unmanaged systems but in most
croplands and forestry plantations as well. We live in a world surrounded by nitrogen but more than
99% of this nitrogen is not available to more than 99% of living organisms. It is all about having enough
of right kind of nitrogen, often called reactive or ‘fixed’ nitrogen converted from the non-reactive N2 form
that determines such fundamentals of life as the extent of plant growth which in turn determines to a
large extent the dynamics of food supply. Since the beginning of the last century, mankind has injected
increasing amounts of reactive nitrogen into the environment, intentionally as fertilizer and unintentionally
as a by-product of combusting fossil fuels. As a result nitrogen cycle is being altered causing possible
2 Bijay Singh, MK Tiwari and YP Abrol

grave impacts on biodiversity, global warming, water quality, human health, and even the rate of population
growth in several parts of the world.
Nitrogen cascade, defined as the sequential transfer of nitrogen through environmental systems
(including temporary storage within each system), leads to multiple linkages among the ecological systems
magnifying the consequences and human health effects of nitrogen. Of course, still there are regions in
developing world, where still not enough reactive nitrogen is available to sustain the human population.
Human activities are responsible for a large proportion of emissions of nitrogen-containing trace gases,
including 40% of the nitrous oxide, 80% or more of nitric oxide, and 70% of ammonia releases on a
global basis. The result is increasing atmospheric concentrations of the greenhouse gas nitrous oxide,
of the nitrogen precursors of smog, and reactive nitrogen that falls from the atmosphere to fertilize
ecosystems. The burning of fossil fuels such as coal and oil releases previously fixed nitrogen from long-
term storage in geological formations back to the atmosphere in the form of nitrogen-based trace gases
such as nitric oxide. High-temperature combustion also fixes a small amount of atmospheric nitrogen
directly. Altogether, the operations of automobiles, factories, power plants, and other combustion processes
emit more than 20 Tg per year of fixed nitrogen to the atmosphere. According to an estimate out of
total emission of 26.77 million tons of NOx in Asia, China and India accounted for 42 and 17% of the
emissions in the year 2000. It is also estimated that by 2020, India alone will be contributing NOx to
the tune of 7.1 million tons annually from road and rail transport sectors. Greatly increased transport
of reactive nitrogen by rivers into estuaries and coastal waters is also a matter of great concern as reports
are already pouring in regarding O2-deficiency in Indian coastal waters due to enhanced nitrogen loading
from land. Since ill effects of excessive reactive nitrogen such as green house effect and damage to ozone
layer due to emission of N2O or acid rain are not confined to political boundaries, developing countries
like India and China which need to support huge populations by producing enough food by increasing
use of nitrogen fertilizers will remain in the eyes of the world until and unless some remedial measures
are taken right now.
The reactive nitrogen is now attracting increased attention from scientists, environmentalists,
governments and industry. Excess nitrogen in our environment represents a human perturbation of the
natural cycle of nitrogen in the environment. Industrial emissions of nitric oxide to the atmosphere must
be reduced as soon as possible. The problem of excess nitrogen can be addressed by more judicious
and efficient applications of nitrogen fertilizer in agriculture, and by better management of wetland
ecosystems that return nitrogen to the atmosphere in its nearly inert or unreactive form, N2. In fact it
is the ultimate goal of the scientific community to provide policy makers with reliable estimates of reactive
nitrogen transfers to different ecosystems and to describe balanced, cost-effective and feasible strategies
and policies to reduce the amount of reactive nitrogen where it is not wanted.

REACTIVE NITROGEN – DEFINITION AND SCOPE

Nitrogen as it exists in its inert state as N2 - is the most abundant element in the earth’s atmosphere
but, in this form, is almost wholly unusable by the vast majority of living organisms. It must be transformed
into a variety of other forms, together called “reactive nitrogen”, in order to be biologically functional.
The diverse pool of nitrogen forms termed as reactive nitrogen includes all biologically, chemically,
radiatively and/or photochemically active nitrogen compounds in the atmosphere and biosphere (Galloway
et al., 1995). It includes forms of nitrogen, such as ammonia (NH3) and ammonium (NH4+), nitric oxide
(NO), nitrogen dioxide (NO2), nitric acid (HNO3), nitrous oxide (N2O), and nitrate (NO3–), and organic
compounds such as urea, amines, proteins and nucleic acids. Structure and functioning of terrestrial,
Reactive Nitrogen in Agriculture, Industry and Environment in India 3

freshwater and marine ecosystems and chemistry and/or radiative balance of the atmosphere are altered
by the availability of reactive N (Vitousek et al. 1997).
Reactive nitrogen can be created both through natural processes and anthropogenically. Under natural
conditions, the triple bond that binds two nitrogen atoms together as N2 is broken either by lightning
or by microbes able to carry the process known as biological nitrogen fixation (BNF). In the oceans BNF
is carried out primarily by cyanobacteria, commonly known as blue green algae. Prior to mid-19th century,
the supply of reactive N for food production was either through BNF, animal manures, rotation of crops
or fallow and it could support the small human population existing during those times. Thereafter with
growth of human population at a very high rate, these sources could not support the needed expansion
of agriculture. In 1900s Haber-Bosch process was invented and it allowed mass production of fertilizer
by synthesizing ammonia from nitrogen and hydrogen. Even after 100 years, this process remains the
most economical anthropogenic means of creating reactive nitrogen and is responsible for sustaining nearly
40 % of the current world population due to its ability to increase crop yields (UNEP and WHRC, 2007).
Where there is not enough reactive nitrogen, soil fertility declines, serious land degradation may occur,
and agricultural productivity is reduced. As a consequence, populations that rely directly on these agricultural
systems cannot produce enough food to survive. However, where too much reactive nitrogen has been
introduced by humans, its positive outcomes can be outweighed by negative ones, ultimately threatening
the very ecosystems it initially supports.
Reactive nitrogen can swiftly move among different media of air, soil and water. It can contribute
to higher levels of ozone in the lower atmosphere, causing respiratory ailments and damaging vegetation.
A portion of reactive nitrogen is converted to nitrous oxide which contributes to both the greenhouse
effect and to stratospheric ozone depletion. From the atmosphere, it can fall to the surface as atmospheric
deposition which leads to acidification of soils and water bodies, and inadvertent fertilization of trees
and grasslands, creating unnatural growth rates, nutrient imbalances, decreasing or altering biodiversity
and corrosion of buildings, bridges and other human made structures,. Leaching out of the soils, reactive
nitrogen can reach groundwater and surface water bodies making them unfit for human consumption
or use. Reactive nitrogen also promotes eutrophication in coastal ecosystems, which can negatively impact
fish stocks and biodiversity. Eventually, most reactive nitrogen is denitrified back to molecular nitrogen.
Abrol et al. (2007) have compiled salient features of cycling of N originating from agrecosystems in terrestrial,
aquatic and atmospheric realms in India.
The most common forms of inorganic nitrogen in the environment are diatomic nitrogen gas (N2),
nitrate (NO3– ), nitrite (NO2–), ammonia (NH3) and ammonium (NH4+). The species that predominate
depend on the chemical, physical, and biological environment. Some reactive N species important in
the context of food production, fossil fuel combustion and environmental degradation are described
below:
NH4+ and NO3– (ammonium and nitrate): The two ionic species of reactive N are abundantly present
in soil solution of terrestrial ecosystems. Roots of plants take N as NH4+ and/or NO3– from soil solution.
Plants can take both the ionic species with equal ease but relative abundance of the two species in the
soil solution is governed by factors such as pH, Eh, aeration status and texture of the soil. At any time,
concentration of NH4+ and NO3– in the soil solution is low but as these are taken up by plant roots
these are replenished through mineralization of soil organic matter and organic manures or through
application of N fertilizers such as urea, ammonium sulphate, calcium ammonium nitrate and anhydrous
ammonia. Role of reactive N in food production is governed by supply of NH4+ and NO3– to crop plants
through biological and anthropogenic sources.
4 Bijay Singh, MK Tiwari and YP Abrol

Nitrate-N in the soil solution can be lost from the root zone via leaching when water percolates
down the soil profile and reach natural water bodies. Nitrate-N is also denitrified to N2O and N2 if anaerobic
conditions occur in the soil and there is sufficient supply of C to denitrifiers. Ammonium-N is readily
adsorbed on soil exchange complex and does not move down the profile in large amounts. However,
it gets converted to NH3 gas if along with high soil pH soil surface gets dried and weather is windy (Bijay
Singh and Yadvinder Singh, 2003).

NOx (nitrogen oxides): Generic term used for a group of highly reactive gases containing nitrogen and
oxygen in varying amounts. Nitrogen oxides are formed when fuel is burned at high temperatures, as
in a combustion process. The primary man made sources of NOx are motor vehicles, electric utilities,
and other industrial, commercial, and residential sources that burn fuels. NOx can also be formed
naturally. Depending upon excess air used during combustion and the gas temperature in the boiler, nitric
oxide (NO) is produced in thermal power plants by the oxidation of atmospheric nitrogen during
combustion of the fuel. The contribution of nitrogen contained in the fuel in the production of NO is
very small. Most of the nitrogen oxides are colorless and odorless. Only exception seems to be nitrogen
dioxide (NO2) which along with particles in the air can be seen as a reddish-brown layer over many
urban areas.
Nitrogen oxides can be transported over long distances and is one of the main ingredients involved
in the formation of ground-level ozone (lowest part of atmosphere extending up to between 8 and 16
km high), which can trigger serious lung damage and respiratory problems. Ozone production in the
troposphere is mainly due to the oxidation of CH4, CO and hydrocarbons in the presence of NOx (Crutzen,
1974; Chameides and Walker, 1973). NOx reacts to form nitrate particles, acid aerosols, as well as NO2,
which also cause respiratory problems. It contributes to formation of acid rain and to nutrient overload
that deteriorates water quality. NOx can contribute to atmospheric particles that cause visibility
impairment. NOx indirectly influences the radiation budget of the atmosphere through O3, which possibly
represents 10–15% of the total anthropogenic greenhouse radiative forcing in the atmosphere (Lacis
et al., 1990, Wild et al., 2001). NOx also influences the oxidation capacity of the atmosphere through
OH and nitrate.

NH3 (ammonia): The atmosphere receives reactive N in the form of NH3 from aquatic and terrestrial
ecosystems. In the atmosphere it is either deposited or transformed into an ammonium aerosol. Before
deposition, ammonium aerosols contribute to fine particulate matter and regional haze concentrations
in the atmosphere. According to Seinfeld and Pandis (1998) and Penner et al. (2001), ammonia plays
an important role in the direct and indirect effects of aerosols on radiative forcing and thus on global
climate change.

N2O (nitrous oxide): When emitted into the atmosphere it disperses and is not rapidly deposited back
to the ground like NOx or ammonia. It has a troposphere residence time of approximately 100 years
and is increasing at a rate of 0.2–0.3% per year (Prather et al., 2001). On a molecule for molecule basis,
N2O has a global warming potential over 200 times greater than that of CO2. Nitrous oxide is a greenhouse
gas in the troposphere but some nitrous oxide makes its way up into the stratosphere where it has another
undesirable effect - it contributes to thinning of the ozone layer. Destruction of stratospheric ozone, which
protects us from harmful effects of UV radiation, is caused by chlorine and bromine released from
halocarbons - the CFCs that have been so widely used in refrigeration, in aerosol cans, insulation and
flame retardants. Nitrous oxide plays its part when it is converted to nitric oxide which acts as a catalyst
in the reactions in which chlorine and bromine destroy ozone.
Reactive Nitrogen in Agriculture, Industry and Environment in India 5

NITROGEN FLUXES, CYCLE AND CASCADE EFFECTS

Nitrogen cycle consists of transformations of molecular nitrogen through fixation into forms of reactive
nitrogen, including those which support the earth’s biota, and back to its molecular state through
denitrification. The cycling of nitrogen among its many forms is a complex process that involves numerous
types of bacteria and environmental conditions. The natural nitrogen cycle has been altered through human
activity in terms of creation of artificial processes to produce more reactive nitrogen to support increased
levels of agriculture. In general, the nitrogen cycle has five steps: (1) nitrogen fixation (N2 to NH3/ NH4+
or NO3–), (2) nitrification (NH3 to NO3–), (3) assimilation (incorporation of NH3 and NO3– into biological
tissues), (4) ammonification (organic nitrogen compounds to NH3) and (5) denitrification (NO3– to N2).
The creation of reactive nitrogen occurs both through natural processes and through human
interventions. Biological nitrogen fixation (BNF) constitutes transformation of gaseous nitrogen into usable
or reactive forms by microbes often existing in a symbiotic relationship with leguminous plants. In the
oceans, BNF is carried out primarily by cyanobacteria, commonly known as blue-green algae.
Anthropogenically, Haber-Bosch process is used to synthesize ammonia from nitrogen and hydrogen gases
and nearly 100 years after its invention, it still remains the most economical means of fixing nitrogen.
Nitrification is a two-step process in which NH3/ NH4+ is converted to NO3–. First, the soil bacteria
nitrosomonas and nitrococcus convert NH3 to NO2–, and then another soil bacterium, nitrobacter, oxidizes
NO2– to NO3–. Assimilation is the process by which plants and animals incorporate the NO3– and NH+ 4
formed through nitrogen fixation and nitrification. Plants take up these forms of nitrogen through their
roots, and incorporate them into plant proteins and nucleic acids. Animals are then able to utilize nitrogen
from the plant tissues. Assimilation produces large quantities of organic nitrogen, including proteins, amino
acids, and nucleic acids. Ammonification is the conversion of organic nitrogen into ammonia. The ammonia
produced by this process is excreted into the environment and is then available for either nitrification
or assimilation. Denitrification is the transformation of reactive nitrogen back to inert gaseous nitrogen
in the atmosphere, carried out primarily by bacteria in soils and water bodies.
Nitrogen cascade is a sequence of effects when excessive reactive nitrogen, in its many forms, readily
moves among terrestrial, aquatic and atmospheric realms accumulating a series of primarily negative
environmental consequences for ecosystems and human health. In Figure 1 Galloway et al. (2003) has
shown multiple linkages among ecological and human health effects of reactive nitrogen molecules as
they move from one environmental system to another.

NITROGEN FLUXES AND CASCADE EFFECTS IN INDIA

Using data from different sources (Bhatt, 2002; FAI, 2000; Agricultural Statistics at a Glance, 1999),
Velmurugan et al. (2008) attempted to quantify different nitrogen fluxes involved in N cycle in agroecosystems
in India. The data shown in Figure 2 were worked out for 1995-96 reference period. In the absence
of reliable quantitative studies, large uncertainties were associated with many estimates shown in
Figure 2, but these seem to be very good estimates to begin with. As better quantification of different
processes and fluxes associated with reactive nitrogen in India become available, improved versions of
nitrogen cycle and cascade effects will become possible in the years to come.
In 1995-96, 10.8 Tg N was applied as nitrogenous fertilizers to agricultural soils in India; another
1.14-1.18 Tg N was added through biological nitrogen fixation. Velmurugan et al. (2008) estimated the
soil N pool other than forest to be as large as 1046 to 2581 Tg N. The proportion of N contained in
soil which is actively recycled in the soil-plant system is not known with certainty. Crude estimates show
that Indian agricultural systems produce annual harvest that removes ~4.13 Tg N from the total crop
6 Bijay Singh, MK Tiwari and YP Abrol

Fig. 1: Illustration of the nitrogen (N) cascade showing the sequential effects that a single atom of N can have in various
reservoirs after it has been converted from a nonreactive to a reactive form. Abbreviations: GH- greenhouse effect;
NH3– ammonia; NO3 – - nitrate; NOx- nitrogen oxide; N2O- nitrous oxide; PM- particulate matter (Source: Galloway et al., 2003)

N pool of ~12.47 Tg N. Further, ~1.9 Tg N is removed from the crop N pool and used for fuel, which
in turn released N2O into atmosphere. The nitrogen contained in plants was either recycled or was supplied
to consumers such as animals (~5.81 Tg N) or people (~0.57 Tg N). India has the largest livestock
population in the world and the livestock biomass N pool was estimated to be ~1.62 Tg of N. The animals
in turn may return a portion of the N to the system as manure. Animals, such as birds or insects also
harvest some N and may return it to the system as excreta and corpse which are difficult to estimate.
Organic manure is one of the important sources of N used in crop production. It is produced from crop,
animal and human wastes and added ~0.17 Tg N to the soil during 1995-96.
The wet N deposition (NO3– and NH4+) in agricultural soils in India during 1995-96 as estimated
by Velmurugan et al. (2008) worked out to be ~0.81 Tg N. Nitrate N leaching beneath agricultural soils
and through runoff was estimated to be ~0.06 Tg N. This agricultural leaching and run-off results in
nitrate pollution of ground water bodies or N enrichment of river systems. Since irrigation is one of the
essential components of modern agricultural production systems, ground water is utilized to irrigate
~36.25 M ha in India. As a result, 0.11 Tg N in the form of NO3– contained in the ground water is
brought back into the agricultural production system. About 25% of N reaching river systems is expected
to end up in the sea. The concentration of NO3–, NO2– and NH4+ in the surface waters of mangroves
in the eastern coast of India near Chennai was found to be very high (35.3, 23.0 and 157μg of the chemical
species l–1 respectively) which are associated with regions receiving agricultural wastewater from land-
based sources (Velmurugan et al. (2008).
Reactive Nitrogen in Agriculture, Industry and Environment in India 7

Fig. 2: Simplified N cycle in agro-ecosystem of India (Velmurugan et al., 2008)

There is substantial movement of N in and out of India from neighbouring countries through wind
and water flows but reliable estimates are hardly available. In 1995-96, 0.07 Tg N comprising food grains
(0.02 Tg N) and animal products (0.05 Tg N) was imported and 0.11 Tg N comprising food grains (0.09
Tg N) and animal products (0.02 Tg N) was exported from India (Velmurugan et al., 2008). Fertilizers
N import which account for 2.00 Tg N (1995-96) is not included in this estimate, but added to the N
fertilizer addition into the soil. The detailed estimation methodology, individual products and N equivalents
are given by Bhatt (2002).
Total N2O emissions from India were in the order of 0.23 Gg in 1990 and 0.26 Gg in 1995 indicating
a marginal growth (Garg et al., 2001). National estimate of N2O emission from manure use is lacking
and most of the research focuses on point/experimental field emission of N2O. Further, reliable estimate
of manure use in agriculture in various districts of the country is hardly available and the existing N2O
emission data at national level is estimated using Inter-governmental Panel on Climate Change (IPCC)
emission co-efficient. The uncertainties associated with such data sets are high as single co-efficient based
estimate can not be reliable.
The NOx emission from India in 1995 was estimated to be 3.46 Tg and grew at about 5.6% per
annum between 1990 and 1995 (Garg et al., 2001a). The regional distribution also indicated a close
relationship with coal as well as oil products consumption. Uttar Pradesh, Maharashtra, Madhya Pradesh,
Andhra Pradesh and Tamil Nadu were the largest five NOx emitting states in 1995 (Garg et al., 2001b).
Total NH3 emission in 2000 was reported to be 7.4 Tg which is 27% of Asian emission (Streets et al.,
8 Bijay Singh, MK Tiwari and YP Abrol

2003). The volatilization of applied N as NH3 and NOx is followed by deposition as ammonium (NH4)
and oxides of nitrogen on soils and water and accounts for indirect NO2 emissions from soils (NATCOM,
2004).

REACTIVE NITROGEN IN INDIAN AGRICULTURE

Agriculture is the mainstay of the Indian economy and it contributes about 22 percent of the gross domestic
product and provides a livelihood to two-thirds of the population. Although livestock rearing is complementary
to agriculture, India has a huge live stock population of over 480 M (IASRI, 2006). The total area under
cultivation is 169.7 M ha; an additional area of 0.4 M ha is under plantation crops (FAOSTAT, 2007).
To meet the food needs of the burgeoning population, India will have to increase the production of food
grains from the present level of 215 M t to 300 M t by 2020. It is an uphill task because prospects for
expanding irrigation, one of the driving forces behind yield increases, are becoming limited as are the
prospects for converting marginal lands into productive arable land. New technologies such as genetically
engineered, yield-increasing plants are also not expected to play major roles in increasing food production
in developing countries during the next two decades. This scenario suggests that future increases in
production of rice, wheat and other cereals will continue to depend heavily on increased use of nutrients,
particularly N, in each hectare of the land under agriculture. Indeed, fertilizer N - an essential component
of green revolution in India – has lead to a tremendous increase in food production since 1960’s.
Consequently, despite large population increases over the same time period, starvation and malnutrition
have declined.
Forms of N (NO3– and NH4+) which are taken up by plants can be made available for crop production
through chemical fertilizers, natural and anthropogenic biological N fixation and through recycling of plant
and animal wastes. Fate of reactive N in agroecosystems assumes great importance because reactive N
fixed biologically or applied as fertilizer not only leads to increased crop production but can also get leaked
from agroecosystems depending on how efficiently it has been used by crop plants. Portion of reactive
N emitted from agroecosystems end up in the form of N2O, NH3, NOx gases, leached as nitrate into
ground and surface water bodies and can reach the coastal waters through rivers; these forms of leaked
reactive N may lead to significant costs to society.
Industrial fixation of N for use as fertilizer represents by far the largest human contribution of new
reactive N to N-cycle. Already, the quantity of fertilizer N used in India during the last 11 years (1995
to 2005) is equal to the total quantity used up to 1994 (FAI, 2005). Area under cereal crops and N use
efficiency are the two major drivers of future N fertilizer consumption in the country. During 1960 to
1990, genetic improvements leading to development of highly fertilizer-responsive rice and wheat varieties
and improved management strategies resulted in a dramatic rise in productivity and production from
rice and wheat in India. For example, more than 75% of the total food grains produced in the country
are rice and wheat (FAI, 2005) and use of nitrogen fertilizers has contributed much to the remarkable
increase in production of rice and wheat in India during more than five decades (Fig. 3).
In the years to come, agriculture in India is going to witness a very delicate balance between inputs
and outputs of reactive N. On the one hand, the demand of burgeoning population for enough and high
protein food will require substantial reactive N inputs into agroecosystems through chemical fertilizers,
biological N fixation and recycling of organic wastes. But on the other hand, to ensure minimal leakage
of reactive N from agriculture to other ecosystems, reactive N must be used efficiently to produce more
food with less reactive N inputs.
Reactive Nitrogen in Agriculture, Industry and Environment in India 9

Fig. 3: Production of rice or wheat in relation to fertilizer N use in India during 1951 to 2004 (Source: FAI, 2005)

Reactive Nitrogen Inputs in Indian Agriculture

Using the approach followed by Parris and Rielle (1999) for some of the OECD (Organisation for Economic
Co-operation and Development) countries, Prasad et al. (2004) computed soil surface N balance for
agricultural land of India for the year 2000-01. Fertilizer N input was calculated by summing the area-
weighted portion of fertilizer sold in each state and multiplying by the N content of the fertilizer. Livestock
manure N production from different states was calculated as the number of live animals distinguished
in terms of general species (sheep, goats, cattle, buffaloes, horses, mules, donkeys, camels, pigs, poultry,
yaks) (Agricultural Statistics at a Glance, 2003) multiplied by respective N excretion coefficients for the
Asian region as given by the Intergovernmental Panel on Climate Change (IPCC,1996). That a large
proportion of animal excreta is not converted to manure and is used for other purposes was not considered
in working out N contributions from livestock manure. Although livestock manures represented a transfer
of already-fixed N from one place to another rather than addition of new reactive N, the data in
Table 1 presents a complete picture of reactive N inputs to agricultural land in India. Interestingly
fertilizer N and biological N fixation – the sources of new reactive N constituted only 44 % of the total
additions.

Table 1. Inputs of reactive N to surface soil of agricultural land of India during 2000-2001

Inputs Total N kg N ha-1


Tg % contribution

Inorganic fertilizers 11.50 32.48 57.76


Livestock manure 15.60 44.06 130.17
Nitrogen fixation 4.10 11.58 17.10
Atmospheric deposition 4.20 11.86 31.81
Source: Prasad et al. (2004)
10 Bijay Singh, MK Tiwari and YP Abrol

The consumption of fertilizers varies significantly from state to state. The all-India per-hectare
consumption of fertilizer N was 59.2 kg in 2003/04 (FAO, 2005). While the North zone had a
consumption of more than 100 kg N ha–1, in the East and West zones the consumption was lower than
50 kg ha–1 (Table 2). Among the major states, the per-hectare consumption of fertilizer N was more than
100 kg in Punjab and Haryana. In Assam, Chattisgarh, Himachal Pradesh, Jammu and Kashmir, Kerala,
Madhya Pradesh, Maharashtra, Orissa and Rajasthan, N consumption per hectare was lower than the
all-India average of 59.2 kg ha–1. Rice occupied an area of 44.7 M ha and it accounted for 31.8 %
(5.34 M t) of total fertilizer consumption in India during 2003/04 (Table 3). Fertilizer N use on irrigated
rice (103 kg ha–1) is almost double that on rainfed rice (56 kg ha–1). Wheat, grown largely under irrigated
conditions, accounts for 20.5 % (3.44 M t) of total fertilizer consumption in India. Fertilizer use per hectare
in 2003/04 was: 137 kg (100 kg ha–1 N, 30 kg ha–1 P2O5 and 7 kg ha–1 K2O). Fertilizer use on irrigated
wheat (144.9 kg ha–1) is almost double that on rainfed wheat and the trend is similar for all the nutrients.
Table 4 reveals that during 1999/2000 to 2003/04, 93.7 to 100 % of fertilizer N applied to agricultural
land was produced in India.
Nitrogen inputs from biological N fixation (field beans, soybeans, clover, alfalfa, pasture) as reported
in Table 1 were obtained from dry biomass production multiplied by the fraction of N in nitrogen-fixing
crops (Prasad et al., 2004). Area under green manuring was about 7 M ha (FAO 2005). Biological
N fixation was found to be high in Andhra Pradesh (71.2 kg N ha–1) followed by Madhya Pradesh
(38.7 kg N ha–1), Maharashtra (36.5 kg N ha–1) and Orissa (34.4 kg N ha–1). The use of biofertilizers
is of relatively recent origin. Biofertilizers consist of N fixers (Rhizobium, Azotobacter, blue green algae,

Table 2. Consumption of fertilizer (kg ha-1) in four zones of India during 2003/04

Zone Fertilizer N Fertilizer N+P2O5+K2O

East (Assam, Bihar, Jharkhand, Orissa, West Bengal) 49.0 75.8


North (Haryana, Himachal Pradesh, Jammu and Kashmir, Punjab, 102.9 140.1
Uttar Pradesh, Uttranchal)
South ( Andhra Pradesh, Karnataka, Kerala, Tamil Nadu) 60.0 105.4
West ( Chattisgarh, Gujarat, Madhya Pradesh, Maharashtra, Rajasthan) 38.0 59.4
All India 59.2 89.8
Source : FAO (2005)

Table 3. Fertilizer use in rice and wheat during 2003-04 in India (Source: FAO, 2005)

Crop Gross cropped Share in fertilizer Fertilizer consumption (kg ha-1)


area (M ha) consumption (%) N P2O5 K2O Total
Rice–irrigated 24.0 22.2 103.4 32.8 18.8 155.0
Rice–rainfed 20.7 9.6 56.6 14.5 6.5 77.6
Wheat–irrigated 22.8 19.7 105.6 32.1 7.3 144.9
Wheat–rainfed 2.9 1.3 55.7 15.9 4.3 75.9

Table 4. Production, import and consumption of fertilizer N in India (000’ t)

1999/2000 2000/01 2001/02 2002/03 2003/04

Production 10,873 10,943 10,690 10,508 10,575


Import 856 164 283 135 205
Consumption 11,593 10,920 11,310 10,474 11,076
Source: FAO (2005)
Reactive Nitrogen in Agriculture, Industry and Environment in India 11

Azolla) and fungi (mycorrhizae). A contribution of 20–30 kg N ha–1 has been reported from the use of
biofertilizers under Indian conditions (FAO, 2005).
The use of organic manures is the oldest and most widely used practice of nutrient replenishment
in India. Prior to the 1950s, organic manures were almost the only sources of reactive N other than
atmospheric N deposition. Organic manures make a significant contribution to the supply of plant nutrients
and soil fertility. Since production of manure is dictated by livestock population, distribution and density
across states and regions of the livestock population are important to study N balances. However, it should
be taken into account that a substantial proportion of cattle excreta is used for purposes other than supplying
nutrients. Thus estimates of total N inputs to agricultural soils as calculated in Table 1 by Prasad et al.
(2004) seem to be on a higher side. At the present production level, the estimated annual production
of crop residues is about 300 M t. As two-thirds of all crop residues are used as animal feed, only one-
third is available for direct recycling (FAO, 2005). The production of urban compost had been
180.8 M t during 1996-97 (IASRI, 2006). In addition to improving soil physical and chemical properties,
the supplementary and complementary use of organic manure also improves the efficiency of mineral
fertilizer use.

Nitrogen Use Efficiency in Agroecosystems

During the last half-decade while fertilizer N consumption in India is touching new heights, the production
of both rice and wheat is plateauing (Fig. 4). In fact, fertilizer N efficiency in food grain production expressed
as partial factor productivity of N (PFPN) has been decreasing exponentially since 1965 (Fig. 5). The
PFPN is an aggregate efficiency index that includes contributions to crop yield derived from uptake of
indigenous soil N, fertilizer N uptake efficiency, and the efficiency with which N acquired by the plant
is converted to grain yield. A decrease in PFPN occurs as farmers move yields higher along a fixed
N response function, unless other factors shift the response function up. The low PFPN during the last
decade is due to low fertilizer N uptake efficiency and is of particular concern for the reactive N budget
because fertilizer N use in India is continuously increasing (Fig. 4). Cassman et al. (2002) defined the

Fig. 4: Time trends of fertilizer N consumption vis-à-vis area and production of rice and wheat in India (Source: FAI, 2005)
12 Bijay Singh, MK Tiwari and YP Abrol

180

160

M t food grain/M t N fertilizer


140

120

100

80

60

40

20

0
1960 1970 1980 1990 2000
Year
Fig. 5: Fertilizer N efficiency of food grain production (annual food grain production divided by annual fertilizer
N application) during 1965 to 2004 in India (Source: FAI, 2005)

overall N use efficiency as the proportion of N inputs that are removed in harvested crop biomass, contained
in recycled crop residues and incorporated into soil organic matter and inorganic pools. Applied N not
recovered in these sinks is prone to loss from the cropping system via leaching, denitrification and
volatilization and contributes to reactive N load that cascades through environment external to the
agroecosystem.
Nitrogen contributions from soil in a given year/season and on a long-term basis can greatly alter
apparent recovery efficiency of applied N (REN) because there occurs a large fertilizer N substitution of
soil N. Although both indigenous soil resources and applied fertilizer N contribute to plant available N
pool consisting of NO3 and NH4 ions, this pool represents a very small fraction of total soil-N. The amount
of N derived from indigenous resources during a single cropping cycle typically ranges from 30-100 kg
N ha–1 that represents only 1.5 to 5% of total soil N. The overall fertilizer N use efficiency can be increased
by achieving greater REN, by reducing the amount of N lost from soil organic or inorganic pools, or both.
When soil-N content is increasing, the amount of sequestered N contributes to higher N use efficiency
and the amount of sequestered N derived from applied N contributes to a higher REN. Conversely, any
decrease in soil N stocks will reduce overall N use efficiency and REN.
A recent review on N use efficiency (Ladha et al., 2005) reported average single-year fertilizer N
recovery efficiencies as 57% for wheat and 46% for rice in researcher managed experimental plots. Nitrogen
recovery in crops grown by farmers, however, is often much lower. A review of best available information
suggests that average N recovery efficiency for fields managed by farmer’s ranges from 20-30% under
rainfed conditions and 30 to 40% under irrigated conditions. Nitrogen use efficiency exceeding 40% is
expected to occur in response to improved N management practices. Cassman et al. (2002) found that
N recovery from on-farm locations averaged 31% for irrigated rice in Asia and 40 % for rice under field
specific management. For wheat grown in India, the recovery averaged 18% under poor weather conditions
but 49% when grown under good weather conditions (Table 5). Ladha et al. (2005) compiled data on
15
N recovery by cereal crops and found that average REN 15N was 44% in the first growing season and
total recovery of 15N fertilizer in the first and five subsequent crops was only around 50%.
Reactive Nitrogen in Agriculture, Industry and Environment in India 13

Table 5. Nitrogen fertilizer recovery by rice and wheat from on-farm measurements (Cassman et al. 2002)

Crop Region Number of farms Average N levels, REN, %


kg N ha-1 (± SD) (± SD)

Rice Asia – farmers practice 179 117±39 31±18


Asia – field specific management 179 112±28 40±18
Wheat India – unfavourable weather 23 145±31 18±11
India – favourable weather 21 123±20 49±10

Management options to enhance fertilizer N use efficiency in agroecosystems has been described
in details by Acharya and Sharma (2007), Pathak and Ladha (2007) and Yadvinder-Singh et al. (2007).
Fertilizer N use efficiency is controlled by crop demand for N, supply of N from the soil, fertilizers and
manures, and losses of N from the soil-plant system (Balasubramanian et al., 2004). Crop N demand
is the most important factor influencing fertilizer N use efficiency. It is determined by biomass yields and
physiological requirements of tissue N. Solar radiation, temperature and moisture regimes determine the
genetic yield ceiling but actual crop yields are far below this threshold because it is neither possible, nor
economical to remove all limitations to growth. Hence, the interaction of climate and management causes
tremendous year-to-year variation in on-farm yields and crop N requirement. Physiological N efficiency
- the change in grain yield per unit change in N accumulation in aboveground biomass is controlled
by mode of photosynthesis (C3 or C4 photosynthetic pathway) and grain N concentration that is also
influenced by N supply (Cassman et al., 2002).

Losses of Reactive Nitrogen from Agroecosystems

Reactive nitrogen leaves agroecosystems through leaching of inorganic nitrate or dissolved forms of
organic N, or through gaseous emissions to the atmosphere in the forms of NH3, NO, N2O, or N2.
Essentially, all emitted NH3 is returned to the surface by deposition (van Breemen et al., 1982).
Atmospheric N deposition may lead to eutrophication of natural ecosystems and loss of biodiversity.
Water management in rice and wheat fields influences the extent of N losses due to nitrification-
denitrification and ammonia volatilization. Up to 50% of the applied N can be lost through
denitrification when alternating aerobic – anaerobic conditions prevail in rice fields. A vast majority
of soils, particularly in the Indo-Gangetic plains, are relatively coarse textured and experience frequent
alternating wetting and drying cycles. Data in Table 6 provides a general idea of gaseous losses of
N occurring in flooded soils. Since these data have been generated from 15N balances, it indicates
losses via ammonia volatilization as well as nitrification-denitrification. Contribution of agriculture to
nitrate enrichment of water bodies and transfer of NH3 and N2O to atmosphere are discussed in
later sections.

15
Table 6. Extent of gaseous N losses computed using N-balance approach from flooded rice soils in India

N application rate (kg ha-1) Method and time of Gaseous N loss Reference
and source N application (% of applied N)

180, Urea Basal 34-50 Rekhi et al. (1982)


180, Urea 3 splits 17-28 Rekhi et al. (1982)
58-116, Urea, (NH4)2SO4 Basal 46-50 Katyal et al. (1985)
100, Urea Basal 58 Mohanty and Mosier (1990)
14 Bijay Singh, MK Tiwari and YP Abrol

Biologically Versus Synthetically Fixed Reactive Nitrogen in Agroecosystems

Before the advent of N fertilizers, farmers used to maintain 25 to 50% of their farm under legume crops
which regenerated soil fertility through biological fixation of atmospheric dinitrogen (N2) by legume–
rhizobial symbiosis. Although the harvested seed of some pulse (edible legume) crops contained much
of the N2 fixed by the legume plants, the residues of such pulse crops still constituted a net N input to
subsequent crops. Legume-based rotations are still common in several parts of India, particularly with
large number of resource poor farmers. As is typical for cereal crops to take up 50% or less of the N
applied as N fertilizers, some legume rotations have also shown similar low N use efficiency (Giller and
Cadisch, 1995; Peoples et al., 1995b; Fillery, 2001). Some times it can be attributed to mismatch between
the timing of nutrient supply and demand in annual cropping systems, although it is generally argued
that legume-based agroecosystems can maintain higher levels of synchrony between N supply and crop
uptake, when compared to single or dual applications of N fertilizers (Becker and Ladha, 1997; Gliessman,
1998). But the data are not conclusive. Some studies showed relatively greater N synchrony in legume-
based systems (Diekmann et al., 1993), but others suggest that fertilizer based systems are superior (Harris
et al., 1994; Cassman et al., 1996). The potential advantage of N fertilized systems is that crops can
receive multiple top-dressings during the growing season to better match N supply with crop N demand
(Cassman et al., 2002). Crews and Peoples (2004) concluded that the ecological integrity of legume-
based agroecosystems is marginally greater than that of fertilizer-based systems. There is thus no marked
difference in N use efficiency between the two systems.
Sufficient data do not exist to state conclusively that legume-N is less susceptible to ammonia
volatilization than fertilizer N (Crews and Peoples, 2004). Nitrate leaching has been found to occur in
both fertilized and legume-based cropping systems (Fillery, 2001; Poss and Saragoni, 1992). However,
when leguminous crops are allowed to grow throughout the fallow season, these not only fix N, but also
scavenge soil available N. Although there are relatively few studies that have directly compared nitrate
leaching in legume and fertilizer-based systems, yet limited evidence suggests that in some cases, nitrate
leaching may be reduced when N is supplied by legumes compared to N fertilizers (Crews and Peoples,
2004). While a few studies have carefully compared N2O fluxes between legume-based and fertilizer-
based farming systems, no direct comparisons have been made of NO fluxes (Davidson and Kingerlee,
1997). Little difference between legume and fertilizer-based agricultures has been reported for N2O
emissions. In a literature review of N2O emissions from 87 different agricultural soils, Bouwman (1996)
reported fluxes ranging between 0 and 4 kg N ha–1 year–1 for unfertilized control plots. Fields planted
with legumes were found to maintain N2O fluxes as low as 0–0.07 kg N ha–1 year–1 (Conrad et al., 1983).

Integrated Management of Reactive Nitrogen Contained in Organic Manures and Chemical


Fertilizers

Despite the fact that organic manures contain almost all the essential plant nutrients and produce several
other non-nutrient benefits, their value was principally assessed in terms of N only (Tandon et al., 1997).
Nevertheless, these studies have revealed that (1) N contribution of organic amendments was highly
variable, unstable, and typically low and (2) organic manures/amendments should supplement and not
supplant nutrient supplies through fertilizers (Katyal et al., 2001). As a result, combined use of chemical
fertilizers and organic manures, referred to as integrated nutrient management, and has emerged as an
important component of the soil fertility management research program in India.
In general, N release from organic amendments is slow and is considered to be better synchronized
with removal of N by crop plants. Efficient integrated nitrogen management systems ensure that fertilizer
N is applied only when adequate amount of N is not being mineralized from organic components. Fertilizer
Reactive Nitrogen in Agriculture, Industry and Environment in India 15

N equivalence of organic materials is thus also influenced by the manner in which fertilizer N was integrated
with organic components of the system. Bijay-Singh et al. (1997) showed that poultry manure-N was
almost as efficient as urea-N in increasing yield and N uptake of rice. On the other hand, rice yield from
combined application of 12 t of farmyard manure (FYM) ha–1 and 80 kg N ha–1 was equal to an application
of 120 kg N ha–1 as fertilizer (Maskina et al. 1988). Efficiency of N added from FYM as compared with
urea, ranged from 42 to 53 % in rice (Yadvinder-Singh et al., 1995).

What can be Done with Increasing Nitrogen Use in Indian Agriculture?


With a population of around 1.1 billion, a growth rate of 1.4% and an ineffective population control
policy, it appears difficult to reduce the population of India in the 21st century. Following the linear relation
(Zheng et al., 2002) between accumulation of N in the environment derived from anthropogenic reactive
N in Asia in the past four decades (Y, Tg, N year–1) with a total population (X, billion) as Y = 22.798*X
– 34.383 (R2 = 0.98, p < 0.001), it does not seem possible to mitigate N-enrichment to any great extent
because Indian agriculture will have to produce food for its burgeoning population by greatly relying on
increasing reactive N. Galloway et al. (2002) lists three specific needs for agriculture if it has to continue
to produce enough food for the masses and at the same time protect the environment from reactive-
N related problems: (1) reduced use of chemical fertilizers, (2) increased efficiency of reactive N use in
food production, including recycling of agricultural wastes, and (3) increased denitrification of reactive
N that cannot be recycled. The first leads to reduced production of reactive N, the second keeps reactive
N in the agroecosystem and also helps achieve the first and the third eliminates the reactive N before
it can leak to the environment. Under Indian conditions, maximum emphasis needs to be given on increasing
N use efficiency in agroecosystems, particularly in rice and wheat based cropping systems as most of
the reactive N is applied to these crops.
Strategies based on applying N at the right amount, right time, and in the right place have already
been developed and are in use. Recent literature on improving N use efficiency has emphasized on achieving
greater synchrony between crop N demand and the N supply from all sources throughout the growing
season (Abrol, 1990; Abrol et al. 1999; Cassman et al. 2002). This approach explicitly recognizes the
need to efficiently utilize both indigenous and applied N because losses of N via different mechanisms
increases in proportion to the amount of available N present in the soil at any given time. Decisions
regarding improvements in fertilizer-N use efficiency will begin at the field scale where farmers need to
deal with the variability in soils, climate, and cropping patterns. As there exists a large fertilizer-N substitution
value of soil N, it is important to know the amount and temporal variations of the indigenous N supply
during crop growth for determining the optimal timing and amount of fertilizer N applications. Since
indigenous N supply is highly variable in the same field over time as well as in different fields within
a given agroecological region (Cassman et al. 2002), accurate predictions are not an easy task. This high
degree of variability and very small size of the indigenously available N relative to much larger background
of total soil N makes the prediction of indigenous soil N supply as one the key challenges for enhancing
fertilizer N-use efficiency. Optimum moisture and temperature, insect and weed management, adequate
supply of nutrients other than N and use of best cultivars all contribute to efficient uptake of available
N and greater conversion of plant N to grain yield. In other words, only a well managed crop can lead
to optimum N use efficiency and profit from applied N along with least possible N losses to the environment
by maintaining plant available- N pool at the minimum size required to meet crop N requirement at each
stage of growth.
Most of the fertilizer-N is lost during the year of application. Consequently, N and crop management
must be fine-tuned in the cropping season in which N is applied. Two broad categories of concepts
and tools have been developed to increase N use efficiency. Those in the first category include genetic
16 Bijay Singh, MK Tiwari and YP Abrol

improvements and management factors that remove restrictions on crop growth and enhance crop
N demand and uptake. Management options that influence the availability of soil and fertilizer-N
for plant uptake come in the second category. These include: site specific N application rates to account
for differences in within-field variation in soil N supply capacity (in large fields), field specific N application
rates in small fields, remote sensing or canopy N status sensors to quantify real-time crop N status,
better capabilities to predict soil N supply capacity, controlled release fertilizers and fertigation. Ladha
et al. (2005) compared different strategies to improve N use efficiency on the basis of benefit cost
ratio and limitations. If a new technology leads to at least a small and consistent increase in crop
yield with the same amount or less N applied, the resulting increase in profit is usually attractive
enough for farmers to adopt such technologies. With very high benefit cost ratio and with no limitation,
use of simple and inexpensive leaf colour chart assists farmers in applying N when the plant needs
it. As the use of leaf colour chart can adequately take care of N supply from all indigenous sources,
it ensures significant increase in REN and reduced fertilizer N use. This tool is particularly useful for
small to medium size farms in developing countries. Similarly, precision farming technologies based
on gadgets like optical sensors have demonstrated that variable rate N-fertilizer application has the
potential to significantly enhance N use efficiency by crops like rice and wheat. Efforts are already
underway to make these technologies available to farmers but it will take some time before these
will become farmer friendly under Indian farming conditions.
Modern N management concepts usually involve a combination of anticipatory (before planting)
and responsive (during the growing season) decisions. Improved synchrony, for example, can be achieved
by more accurate N prescriptions based on the projected crop N demand and the levels of mineral and
organic soil N, but also through improved rules for splitting of N applications according to phenological
stages, by using decision aids to diagnose soil and plant N status during the growing season (models,
sensors), or by using controlled-release fertilizers or inhibitors. Important prerequisites for the adoption
of advanced N management technologies are that they must be simple, provide consistent and large enough
gains in fertilizer N use efficiency, involve little extra labour and be cost-effective.

Reactive Nitrogen in Animal Agroecosystems

Animal agroecosystems produce dietary protein (milk, eggs, and edible meat) from the consumption of
proteins produced by crop agroecosystems. Depending on animal species, ration and management,
between 5 % and 45 % of the N in plant protein is converted to and deposited in animal protein. The
other 55 % – 95 % is excreted via urine and feces, and can be used as nutrient source for plant production.
As in crop agroecosystems, most of the reactive N that enters the animal agroecosystem is lost to the
environment over the course of a year (Galloway et al., 2003). Cattle, sheep and pigs have the largest
share in animal manure N production. The conversion of plant N into animal N is on average more
efficient in poultry and pork production than in dairy production, which is higher than in beef and sheep
production. Typical rates of N-use efficiency for production of human-digestible protein from feed grains
and forages on farms are about 50 % to 60 % for fish, about 40 % to 50 % for poultry, about 35%
to 40% for dairy and about 15 % to 30 % for beef (Galloway et al., 2003). The efficiency of the conversion
of N from animal manure, following application to land, into plant protein ranges between 0 and
60 %, while the estimated global mean is about 15 %. The other 40 % – 100 % is lost to environment
via NH3 volatilization, denitrification, leaching and run-off during storage and/or following application
of the animal manure to land. Relative large losses occur in confined animal feeding operations, as these
often lack the land base to utilize the N from animal manure effectively. Nitrogen conversion in animal
production systems can be improved by manipulating composition of the animal feed and proper
Reactive Nitrogen in Agriculture, Industry and Environment in India 17

management of the animal manure. Of the total N consumed by animals, about 15 % is consumed by
humans. The remaining reactive N is lost as manure and waste (Smil 2001, 2002). Coupling of crop
and animal production systems, at least at a regional scale, is one way to high N use efficiency in the
whole system.
The negative growth rate was recorded in cattle population in India in recent years (16th Indian
Livestock Census, 2003; 17th Indian Livestock Census, 2005) due to mechanization in agriculture and
economic considerations. Gupta et al. (2007) calculated the bovine population in the country in 2000
as more than 271 × 106 (Table 7). Total dry matter consumed by bovine in India during 2000 was of
the order of 471 Tg. Out of 210 Tg dung produced, only around 80 Tg was used as manure; similar
quantity was used for making dung cakes (Table 8). Dung cake is utilized in most of the states of India,
except Himachal Pradesh, Jammu and Kashmir and North-Eastern states and is less utilized in Kerala
and Delhi (Gupta et al., 2007). Manure management includes storage and treatment of manure, before
using it as farm manure or burning as fuel. Production of N2O from animal manure depends on digestibility
and composition of feed, species of animals and their physiology, manure management practices. Nitrous
oxide emission factors and total emission from manure management in India has been discussed in a
subsequent section.

Table 7. Bovine population, dry matter excretion, N2O emission factors and emission estimates from bovine
manure management in India for the year 2000 (Adapted from Gupta et al., 2007)

Category Age Dry matter excreted Population N2O emission N2O emission
(kg head-1 day-1) (× 1000)† factor (mg head-1 year-1) (kg)

Dairy indigenous Adult 1.93 ± 0.06 47877 9.7 ± 1.9 465.2 ±91.8
Dairy crossbred Adult 2.35 ± 0.07 8865 8 ± 1.6 70.9 ± 14
Non-dairy cattle Below 1 year 0.79 ± 0.02 17249 3 ± 0.6 52.2 ± 10.3
(indigenous) 1-3 year 1.88 ± 0.05 30758 6.5 ± 1.3 200.3 ± 39.5
Adult 2.61 ± 0.07 68345 8.9 ± 1.7 605.5 ± 119.5
Non-dairy cattle Below 1 year 0.73 ± 0.02 3290 3.3 ± 0.6 10.8 ± 2.1
(crossbred) 1-2.5 year 1.57 ± 0.04 3819 7.8 ± 1.5 29.6 ± 5.8
Adult 2.14 ± 0.06 3943 10.8 ± 2.1 42.6 ± 8.4
Dairy buffaloes Adult 2.65 ± 0.08 44295 11.0 ± 2.2 485.3 ± 95.7
Non-dairy buffaloes Below 1 year 1.26 ± 0.04 14090 5.2 ± 1 73.6 ± 14.5
1-3 year 2.4 ± 0.07 16362 9.9 ± 2 162.4 ± 32
Adult 2.83 ± 0.08 12422 11.7 ± 2.3 145.5 ± 28.7
Total 271314 2343.8 ± 462.4
†Compounded annual growth rate in bovine population between 1997 and 2003 (16th Indian Livestock Census, 2003; 17th
Indian Livestock Census, 2005) was applied to the population recorded in 16th livestock census to obtain population for the
year 2000 and animals below 3-months age group were excluded, due to their negligible dry matter excretion.

Table 8. Use pattern of bovine dung produced in India during 2000 (Adapted from Gupta et al., 2007)

Type of use % of total Quantity (Tg)

Dung cake 38.4 80.5


Biogas 7.4 15.6
Rangeland 14.0 29.4
Slurry and lagoon 1.0 2.1
Others 1.0 2.1
Manure 38.2 80.2
Total 209.8
18 Bijay Singh, MK Tiwari and YP Abrol

REACTIVE NITROGEN FROM USE OF FOSSIL FUELS IN INDUSTRY, TRANSPORT AND ENERGY
PRODUCTION IN INDIA

Fossil fuel combustion is a major source of NOx inputs to the atmosphere. There are two broad categories
of sources for these emissions. Thermal NOx is generated by the oxidation of diatomic nitrogen as a
by-product of combustion. In the second category, fuel NOx is formed when the nitrogen contained in
the organic compounds that comprise fossil fuels is released to the atmosphere. While thermal NOx is
dominant for fuels with low nitrogen content such as natural gas and petroleum distillates, fuel NOx which
accounts for 50–90 % of the emissions associated with heavier fuels such as residual oil and coal containing
between 0.3% and 3.0 % N by weight (Seinfeld 1986). Estimations of NOx emissions are often not subject
to direct measurement but are instead inferred from data on fuel use. The consumption of different energy
carriers such as hard coal, lignite, gasoline, residual fuel oil, natural gas, is multiplied by average emission
coefficients that are derived from field observations and/or laboratory studies (Müller 1992). This approach
is useful in generating order-of-magnitude emission estimates, but is unable to account for the role of
specific technologies in mediating the relationship between fuel use and NOx emissions. This method,
however, is often the best that can be done to estimate NOx emissions in developing countries, where
disaggregated data on the disposition of fuel consumption by end use or process are often of low quality
or are entirely lacking (Mosier et al. 2002).
Garg et al. (2006) have attempted to provide aggregated energy consumption major fuel categories
in India during 1985-2005. These data as listed in Table 9 along with default emission factors for different
source categories (IPCC, 1996) were used by Garg et al. (2006) as the basis for working out NOx emissions
from energy sector. Wherever possible India specific emission factors were used. The NOx emissions from
mobile vehicles are related to the air–fuel mix, combustion temperatures and the pollution control devices
installed in the vehicle. Diesel vehicles emit more NOx as compared to petrol driven vehicles. NOx emission
from heavy-duty vehicles is significantly higher than those for cars and light commercial vehicles. Other
than these fossil fuel combustion source categories for NOx emissions, nitric acid production is the main
non-energy source of NOx emissions (Garg et al., 2006). Nitric acid is produced from the catalytic oxidation
of ammonia and nitrogen oxides are released in the process. Emissions are estimated from the amount
of nitric acid produced.
Data pertaining to NOx emissions in India as listed in Table 10 (Garg et al., 2006) reveals that around
2.11 Tg NOx were emitted in 1985 and these were increasing at a rate of about 4.5% per annum between
1985–2005. Coal (mainly in power generation sector) and oil combustion have almost equal shares in

Table 9. Energy consumption during 1985–2005 in India (Garg et al., 2006)

Fuel type Units 1985 1990 1995 2000 2005

Bituminous coal Tg 116.7 165.8 231.2 289.0 347.0


Lignite Tg 8.1 13.8 21.8 22.7 31.0
Coking coal Tg 36.5 47.7 51.9 51.6 56.2
Natural gas BCMa 4.2 10.9 19.1 23.3 31.0
Oil products Tg 43.3 58.6 78.8 108.8 132.0
Motor gasoline Tg 2.3 3.5 4.7 6.6 9.0
Diesel Tg 15.9 23.6 34.9 42.0 43.0
Kerosene Tg 6.2 8.4 9.9 11.3 12.6
Heavy fuel oil Tg 9.6 10.8 12.9 16.2 18.6
Sources: Synthesized and compiled from CMIE (2000, 2005), OCC (1998), INC (2004) Enerdata database; IEA (2003); BCM
(Billion Cubic Meter)
Reactive Nitrogen in Agriculture, Industry and Environment in India 19

Table 10. NOx emissions from different sectors in India (Tg –NOx)

Source categories 1985 1990 1995 2000 2005 CAGR % (1985-2005)

Power 0.377 0.620 0.964 1.283 1.547 7.3


Road 0.520 0.670 0.985 1.380 1.696 6.1
Rail 0.120 0.101 0.100 0.110 0.132 0.5
Navigation 0.010 0.012 0.014 0.018 0.023 4.3
Aviation 0.018 0.024 0.033 0.042 0.051 5.4
Cement 0.040 0.060 0.085 0.116 0.148 6.7
Steel 0.123 0.152 0.181 0.206 0.231 3.2
Brick 0.078 0.094 0.109 0.133 0.165 3.8
Other industries 0.204 0.229 0.263 0.287 0.315 2.2
Biomass burning 0.586 0.633 0.670 0.670 0.630 0.5
Nitric acid production 0.002 0.004 0.006 0.011 0.013 9.8
Other sectors 0.030 0.040 0.046 0.049 0.051 2.7
All India (Tg NOx) 2.110 2.640 3.460 4.31 5.020 4.4
Source: Garg et al. (2006)

total NOx emissions. Road transport sector is the predominant source of NOx emissions contributing 34%
to Indian emissions in 2005. Emissions from diesel combustion in transport sector have more than doubled
during 1985–2000. Power generations followed by industry are the next largest contributors. Analysis
of changing sectoral NOx emission shares during 1985–2005 indicates an increase in power sector share
from 18% to 30% and road transport from 25% to 33% (Garg et al., 2006). On the contrary, the emission
share of biomass burning has declined from 28% to 15%, other industries (10–6%) and railways
(6–3%). It must be noted here that absolute emissions from all these sources have increased during this
period. Differential growth rates result in changing emission shares.
Using the default IPCC emission factors Singh et. al. (2007) estimated that the Indian road transport
sector contributed about 0.3 Tg NOx emissions in 1980 which increased to 1.1 Tg in 2000. The diesel-
powered vehicles were the dominant contributors and account for about 84% of the total NOx emissions
for the road transport sector. It could possibly be due to higher consumption of diesel in freight and passenger
(mass transport) transport vehicles which are mostly powered by diesel engines.
Field burning of crop residues constitutes an important source of NOx in India. According to Gupta
et al. (2004), 40 Gg of NOx were emitted in 1994 due to field burning of wheat residues in the country.
Recently, Sahai et al. (2007) estimated that the field burning of wheat residue was responsible for emissions
of 33±32 Gg of NOx for the year 2000.
Recently Ohara et al. (2007) developed a new emission inventory for Asia called Regional Emission
Inventory in Asia (REAS) for the period 1980–2020. REAS is the first inventory to integrate historical,
present, and future emissions in Asia. Emissions were estimated on the basis of activity data at district
levels for China, India, Japan, South Korea, and Pakistan. For the other countries, national emissions
were estimated on the basis of activity data at the national level. Emissions of NOx from fuel combustion
sources and non-combustion sources as part of anthropogenic activities were estimated from transformation
(power) sectors (electricity and heat production, oil refineries, manufacture of solid fuels, and other energy
and transformation industries); industry sectors (including iron and steel, chemical and petrochemical,
non-ferrous metals, and non-metallic minerals); transport sectors (including aviation, roads, railways, and
shipping); and other (mainly domestic) sectors (including agriculture, commerce and public, and residential).
Emissions were estimated as a product of the activity data, emission factors, and removal efficiency of
20 Bijay Singh, MK Tiwari and YP Abrol

emission controls. Region-specific emission factors for several emission species from subdivided source
sectors were developed from a wide range of sources and were used to estimate emissions on district
and country levels. The estimates on district and country levels were divided into a 0.5°×0.5° grid by
using index databases – population data; information on the positions of large point sources; land cover
data sets and land area data sets. On-road vehicles were classified into seven types (light-duty gasoline
vehicles, heavy duty gasoline vehicles, light-duty diesel vehicles, heavy-duty diesel vehicles, gasoline buses,
diesel buses, and motorcycles). Motor gasoline and diesel oil consumption was distributed to each vehicle
type by using traffic volume and fuel economy data, and then the emissions were estimated by using
country-specific emission factors by vehicle type.

Table 11. National NOx emissions in Asian countries during 2000 (Adapted from Ohara et al., 2007)

Country NOx (kt year-1)

India 4730
China 11186
Japan 1959
South Korea 1559
Indonesia 1653
Pakistan 640
Thailand 591
All Asia 27316

Table 12. Fuel consumption (PJ) between 1980 and 2003, mean emission factors for fuel combustion in 2000
and NOx emissions in 2000 by region, sector and fuel type in India and Asia (Adapted from Ohara
et al., 2007)

Region Year Power plants Industry Transport Domestic Total


Coal Oil others Coal Oil others Oil others Coal Biofuel others

Fuel consumption (PJ)


India 1980 902 120 18 565 525 906 472 229 323 5920 284 10263
1990 2481 150 145 1141 865 1321 996 102 464 7051 514 15229
2000 5201 325 422 874 2382 1741 1273 0 355 7866 948 21387
2003 5655 310 567 987 2470 1758 1313 0 388 8239 1088 22776
China 1980 2410 963 105 5498 1605 875 640 402 3017 4751 595 20860
1990 6046 659 193 8836 8518 1439 1145 430 4655 5788 908 32618
2000 12679 604 457 10828 4447 1991 2726 236 3055 5289 2207 44520
2003 18584 714 440 13040 5436 2689 3347 239 3102 5401 2651 55644
Asia 1980 3856 4679 1325 7537 7738 3752 4385 634 3917 15602 3563 56986
1990 10248 4086 2815 11905 9804 6130 7360 532 5670 18532 5313 82395
2000 22284 3566 5766 13751 17070 8936 12135 241 3625 19420 8697 115490
2003 29984 3217 7011 16443 19121 10083 13262 264 3707 20172 9296 132559
Mean NOx emission factors for fuel combustion in 2000
China 298.8 279.2 161.2 241.8 79.8 78.6 1017.1 241.2 95.0 82.9 110.8 246.3
Asia - other 267.0 303.1 189.8 240.7 81.2 79.7 921.1 79.7 122.9 81.4 74.1 157.3
than China
and Japan
Regional NOx emissions in 2000 (kt year-1)
India 1543 185 81 249 228 161 1564 0 45 618 56 4730
China 3788 169 74 2839 357 156 2773 57 290 439 245 11186
Asia 6012 842 717 3695 1217 690 9169 57 361 1588 763 27316
Reactive Nitrogen in Agriculture, Industry and Environment in India 21

Total emissions of NOx in Asia were 27.3 Mt in 2000 (Table 11); China at 11.2 Mt (65%) and India
at 4.7 Mt (17%) were high-emission countries. Japan (7%), South Korea (6%), and Indonesia (6%) also
made relatively large contributions. Table 12 lists sectoral and fuel-type consumption, mean emission factors
and emission of NOx for India, China and Asia as worked out by Ohara et al. (2007) following REAS.
On Asia basis, NOx emissions from transport oil use were the largest (34%), followed by coal use in
power plants (22%) and industrial coal use (14%). For contributions by fuel type alone, oil use (41%)
was slightly greater than coal use (37%). In China, the country with the largest emissions, coal-burning
power plants were the largest emitters (34%), followed by industrial coal use and transport oil use (both
at 25%). In India, the contributions of coal-burning power plants and transport oil use were dominant
(both at 33%). Additionally, domestic biofuel use was a large contributor (13%) – larger than in
China (4%).
Ohara et al. (2007) compared the Asian total NOx emissions for 2000 as estimated by REAS and
other inventories and found that the REAS value (25.1 Mt) was almost the same as the IIASA one (25.8
Mt), whereas the TRACE-P value (22.7 Mt) was 10% lower, and that of EDGAR (31.1 Mt) 24% higher,
than the REAS value. For Indian NOx emissions (Table 13), the REAS (4.7 Mt) and IIASA (4.6 Mt) values
were very close, whereas the TRACE-P value (4.0 Mt) was slightly lower, and the EDGAR (6.3 Mt) value
higher, than the REAS and IIASA values.
Total emissions of NOx in Asia between 1980–2003 showed a monotonic increase with no dips.
Sectoral contributions to Asian NOx emissions revealed that emissions from the power plants, industry,
transport, and domestic sectors contributed 17%, 29%, 37%, and 17%, respectively, in 1980 and 33%,
22%, 35%, and 10%, respectively, in 2003 (Ohara et al., 2007). Contribution of power plants almost
doubled between 1980 and 2003. Indian and other South Asian NOx emissions in 2020 were estimated
at 7.1 Mt and 2.2 Mt, respectively (Table 14) – a rapid growth in emissions (by 49% in India and 122%
in other South Asia) compared with 2000 levels (Ohara et al., 2007).

Table 13. Comparison of estimates of NOx emissions in India during 1995 and 2000a (kt year-1) (Adapted
from Ohara et al. 2007)

Study 1995 2000

Garg et al. (2001) 3460 –


Streets et al. (2001) 4500 –
Streets et al. (2003) TRACE-P – 4047
Ohara et al. (2007) IIASA 3470 4563
Ohara et al. (2007) EDGAR 3.2 5347 6285
Ohara et al. (2007) REAS 4377 4730
excluding emissions from open biomass burning
a

Table 14. Projected regional NOx emissions (kt year–1) in 2010 and 2020 (Adapted from Ohara et al. 2007)

Region 2000 2010 2020

India 4730 5900 7052


South Asia other than India 992 1496 2201
China 11186 13990 15619
Japan 1959 1837 1837
All Asia 25112 31093 36124
22 Bijay Singh, MK Tiwari and YP Abrol

Studies based on in situ observations over several locations in India indicate that the rural atmosphere
is significantly influenced by the urban emission of NOx by transport and mixing (Chand and Lal, 2004;
Varshney and Agarwal, 1992). As India is highly heterogeneous with respect to different agroclimatic features
and with respect to emissions from urban and rural areas, synergetic use of a chemical transport models
and satellite observations has been attempted by Kunhikrishnan et al. (2006) for better understanding
of the NOx-related chemistry over India. They examined the regional characteristics of NOx induced
chemistry over India using output from the global model, Model of Atmospheric Transport and Chemistry
–Max Planck Institute for Chemistry Version (MATCH-MPIC), retrievals of the tropospheric NO2 column,
and corresponding emission estimates from the Global Ozone Monitoring Experiment (GOME) instrument
on board the ERS-II satellite, including an examination of the quality of the O3 simulation with respect
to available MOZAIC profiles over India. They concluded that the mean regional NOx emission strength
for India is close to 2.5 Tg N year–1 with a seasonal maximum (~3 Tg N year–1) during April and minimum
(~1.6 Tg N year–1) during winter. The changes in the O3 concentrations with respect to NOx and non-
methane hydrocarbon emissions from India show that southern India is relatively more sensitive to local
emissions.

ATMOSPHERIC NITRIC OXIDE (NO) AND NITROUS OXIDE (N2O)


The NO emission from Asian cultivated soils (excluding the burning of crop residues) in 1980s and 1990s
has been estimated at 0.8–1.2 Tg N year–1 (Zheng et al. 2002), which accounts for 16–24% of the global
total ranging from 1.6 to 8.4 Tg N year–1 (Davidson and Kingerlee, 1997; Delmas et al. 1997). Using
modeling approach, Mittal and Sharma (2007) reported NO emission per unit of electricity in India as
~4.8 g kWh–1. This compares to a U.S. average 3.5 ~4.8 g kWh–1 for the year 1995. For the year 1997,
total NO emissions due to thermal power generation and vehicular transport in India were estimated
as 5.3 and 4.83 Tg, respectively. According to an estimate made by Sahai et al. (2007), 15±14 Gg NO
was produced from field burning of wheat residues in India during 2000.
The global atmospheric nitrous oxide concentration increased from a pre-industrial value of about
270 ppb to 319 ppb in 2005 (Fig. 6). The growth rate has been approximately constant since 1980.
More than a third of all nitrous oxide emissions are anthropogenic and are primarily due to agriculture
(IPCC, 2007). Bouwman (1996) compiled data on N2O emissions from 87 different agricultural soils and
reported fluxes ranging between 0 and 30 kg N2O-N ha–1 per year with unfertilized control plots ranging
between 0 and 4 kg N ha–1 per year. Fields planted in legumes have been found to maintain N2O fluxes
as low as 0–0.07 kg N ha–1 per year (Conrad et al., 1983). The estimate of N2O emission from agricultural
soils and manure management in Asia for 1990s ranged from 1.1 to 1.4 Tg N year–1, accounting for
17–32% of the latest global estimates of 3.9–6.3 Tg N year–1 (IPCC, 2001). Of the total anthropogenic
emissions of NOx and N2O from Asian agriculture, about 68% is due to the combined contributions of
India and China.
Following IPCC methodologies (IPCC, 1996; Garg and Shukla, 2002), Garg et al. (2006) estimated
direct N2O emissions from soils (including use of synthetic fertilizers), field burning of agriculture crop
residue, manure management, indirect soil emissions, fossil fuel combustion, industrial activities namely
production of nitric acid, and waste sector in India (Table 15). Taking 178 Gg–N2O emissions for 1994
as benchmark, there has been a noticeable lowering in direct N2O emission estimates from soils, including
from use of synthetic fertilizers. This is mainly due to the use of India specific emission factors that are
lower by almost 30% than the IPCC default values. The previous emission factors were 0.93 kg ha–1
N2O–N for all types of crop regimes. The revised emission factors used for rice–wheat systems are 0.76
for rice and 0.66 kg ha–1N2O–N for wheat for urea application without any inhibitors (Pathak et al., 2004).
Agriculture sector activities account for more than 80% of the total N2O emission including 60% from
Reactive Nitrogen in Agriculture, Industry and Environment in India 23

Fig. 6: Atmospheric concentrations of nitrous oxide over the last 10,000 years (large panels) and since 1750 (inset panels).
Measurements are shown from ice cores (symbols with different colours for different studies) and atmospheric samples (red
lines). The corresponding radiative forcings are shown on the right hand axes of the large panels. (Source IPCC, 2007).

Table 15. N2O emissions from various source categories in India in Gg-N2O (Source: Garg et al. 2006)

Source categories 1985 1990 1995 2000 2005 Compounded annual growth rate (%)

Synthetic fertilizer use 80 94 109 129 151 3.2


Field burning of agricultural residues 15 18 21 21 20 1.4
Indirect soil emissions 17 19 21 25 30 2.9
Manure management 4 5 6 6 8 3.9
Fossil fuel combustion 7 9 12 15 19 4.9
Industrial processes 6 7 9 12 16 5.0
Wastes 5 6 7 8 9 2.8
Total N2O 134 158 185 217 253 3.2

use of synthetic fertilizer, about 12% each from agriculture residue burning and indirect soil emissions
and about 3% from manure management (Garg et al., 2006).
Production of N2O occurs by both nitrification and denitrification during storage of animal manures.
Emission factors for N2O for solid storage of animal manure in India as worked out by Gupta et al. (2007)
varied from 3 to 11.7 mg head–1 year–1for different categories of bovine with a total annual emission
estimate of about 2344 kg N2O for the country (Table 7). Indigenous cattle were responsible for higher
emission due to their larger population followed by buffalo and crossbred cattle.
Using geographical information system (GIS) interfaced Asia-Pacific Integrated Model (AIM / Enduse),
which employs technology share projections for estimating future N2O emissions, Garg et al. (2004) analyzed
reference scenarios and concluded that agriculture sector activities will account for more than 90% of
the total N2O emissions in India presently, including 66% from the use of synthetic fertilizers, about 10%
24 Bijay Singh, MK Tiwari and YP Abrol

each from field burning of agriculture residues and indirect soil emissions, and about 5% from livestock
excretions. Use of synthetic fertilizers is the single largest source of N2O emissions presently and is projected
to retain this prominence in future (Table 16). Figure 7 shows the N2O emissions in the reference scenarios
for the years 2000 and 2020. The contribution of the agriculture sector, especially due to the use of synthetic
fertilizers, is the dominant source of emissions, though it varies across the states.

EMISSION OF REACTIVE NITROGEN AS AMMONIA FROM TERRESTRIAL ECOSYSTEMS

Application of fertilizers and the livestock in agriculture sector are the major contributors to NH3 emissions.
The estimates of NH3 in India are, however, highly uncertain as no country specific emission factor for
NH3 is available as yet. Using emission factors proposed by Asman (1992), Parashar et al. (1998) estimated
that the fertilizers applications were responsible for emission of about 1.17 Tg NH3 during 1993-94. Out
of all the fertilizers, the urea application is responsible for more than 90 % of the total contribution due

N2O ‘tons
0
750
1500
2250
3000
3750
4500
5250
2000 >=6000 2020
Fig. 7: N2O emissions in India in the reference scenarios 2000 and 2020 (Source: Garg et al. 2004)

Table 16. N2O emission projections for India under the reference scenario

Source (Gg) 2000 2010 2020 2030

Coal combustion 9.9 16.8 24.0 28.0


Oil product combustion 2.0 3.6 6.4 10.0
Field burning of agricultural residue 33.9 41.5 42.6 33.4
Biological nitrogen fixation 5.6 6.6 7.8 9.1
Natural gas combustion 0 0 0 0
Synthetic fertilizer use 206.1 368.4 524.9 626.8
Livestock 12.2 14.1 16.3 18.8
Industrial processes 12.1 23.0 31.0 38.0
Indirect emissions 26.0 30.7 36.2 42.6
Total N2O (Gg) 307.8 504.6 689.0 806.7
Reactive Nitrogen in Agriculture, Industry and Environment in India 25

to fertilizers. Loss of N via ammonia volatilization can be substantial when urea is top dressed. Placement
of urea on the wet surface of alkaline soils promotes ammonia volatilization. If applied on the wet soil
surface following irrigation, as much as 42% of the applied 15N was lost due to volatilization (Katyal
et al., 1987). However, deep placement of urea due to its application before irrigation and resultant reduction
in losses of applied 15N from 42 to 15 % is also demonstrated from the work of Katyal et al. (1987).
Ammonia volatilization losses of reactive N fixed by legumes or applied through fertilizer N can
be substantial, especially in regions that are irrigated and/or have alkaline soils. Ferm (1998) observed
that about half of the ammonia that is volatilized is deposited in downwind ecosystems within a 50 km
radius, while the other half is deposited over a much broader region. Losses of ammonia following fertilizer
applications to upland and lowland cropping systems can range from ~0 to >50%, while losses from
flooded rice can reach as high as 80% (Peoples et al., 1995a). Fertilizer placement, the timing of application,
soil temperature and fertilizer type determine loss rates (Peoples et al., 1995a). Ammonia volatilization
from legume residues may be high when they are left on the soil surface, but the losses do not appear
to match those measured in some fertilized systems.
The contribution of livestock have been estimated to be 1.43 Tg of NH3 during 1993-94 (Parashar
et. al. 1998). Out of these emissions, the cattle have been estimated to have the largest contribution
amounting to 1.05 Tg followed by buffaloes which have been estimated to contribute about 0.28 Tg
NH3. The other categories of livestock like pigs, poultry, horses and sheep had very small contributions
in the total national NH3 emissions. These emission estimates were based on the emission factors proposed
by Asman (1992) were developed using the feed intake ratios of West European cattle and may not truly
represent Indian conditions where the feed intake ratios are generally low.
Based on the available data from different stations in India, Kulshrestha et al. (2005) conducted
precipitation monitoring studies to work out regional patterns. The lowest NH4+ median concentrations
of 9 μeq l–1 in the precipitation was observed over rural areas whereas a value of 14 μeq l–1 was recorded
for sub-urban areas. The urban areas precipitation showed the highest NH4+ median concentration of
22 μeq l–1; the industrial areas recorded a median value of 18 μeq l–1. The median depositional fluxes
of NH4+ species over rural, suburban, urban and industrial areas were estimated to be 10, 13, 18, 26
μeq m2 yr–1, respectively (Kulshrestha et al., 2005). Although urban areas show high depositional flux
of NH4+, values for rural areas are also substantially high and should contribute significant amount of
N to agricultural soils. However, no quantitative estimates are yet available for Indian conditions.
According to estimates made by Zheng et al. (2002), reactive N in Asia was transferred to the
atmosphere by NH3 volatilization at a rate of ~ 4.6 Tg N year–1 in 1961 which increased to
~ 13.8 Tg N year–1 in 2000. It is expected to reach ~ 18.9 Tg N year–1 in the next three decades. China’s
contribution increased from ~ 25% in 1961 to ~ 39% in 2000, while India’s contribution decreased
from ~ 41% in 1961 to ~ 29% in 2000. In the next three decades, however, the contribution of China
is expected to decrease to ~ 35% and that of India is anticipated to remain at ~ 29%. The NH3
released to the atmosphere is redeposited to downwind terrestrial lands at a rate ranging from
3.8 Tg N year–1 in 1961 to 15.7 Tg N year–1 in 2030, while the deposition to coastal waters stands at
a rate of 0.8–3.4 Tg N year–1 over 1961–2030. As per estimates given by Zheng et al. (2002) human-
excreted N, the temporal variation in livestock-excreted N is an indicator of the growth of animal husbandry
in Asia. As Figure 8 shows, livestock production developed very rapidly in the 1980s–1990s. But its
development rate in the coming decades is expected to be slower and almost equal to that of
1960s–1970s.
26 Bijay Singh, MK Tiwari and YP Abrol

Fig. 8: Livestock- and human-excreted nitrogen and its ammonia volatilization in Asia (Source: Zheng et al. 2002)

NITRATE-NITROGEN IN GROUNDWATER BODIES

Nitrate-N levels in relatively pollution free regions of world such as high altitude lakes and rivers and
snow clad mountains in central Himalayas is about 0.11 mg N l–1 (Sarin et al., 1992). According to Agrawal
et al. (1999), water in a relatively pure system contains less than 0.22 mg N l–1 and concentrations higher
than this reflect anthropogenic or geological contributions. In oceans, which are the ultimate sink for
terrestrial water, the average nitrate-N levels are 0.15 mg N l–1 (Mason and Moore, 1985). The United
States Environmental Protection Agency (EPA) considers 3 mg NO3-N l–1as the level beyond which human
activities may be taken as contributing nitrogenous compounds to the water bodies (Anonymous, 1987).
The World health Organization (WHO) has recommended the limit of 10 mg NO3–N l–1 for drinking
water which is equivalent to about 45 mg NO3 l–1 and it has also been accepted in India by the Indian
Council of Medical Research.
Although studies have been performed attempting to link nitrate consumption to various illnesses,
only methaemoglobinemia, (infant cyanosis or blue-baby syndrome) has been proven to result from
ingestion of water containing nitrate concentrations more than 10 mg NO3–N l–1 (Kross, 1993). Methaemoglobin
is probably formed in the intestinal tract of an infant when bacteria convert the nitrate ion to nitrite ion
(Comly, 1987). One nitrite molecule then reacts with two molecules of hemoglobin to form methaemoglobin.
This altered form of blood protein prevents the blood cells from absorbing oxygen which leads to slow
suffocation of the infant which may lead to death (Gustafson, 1993). An epidemiological investigation
undertaken to assess the prevalence of methaemoglobinemia in areas with high nitrate concentration
drinking water in Rajasthan in India revealed severe methaemoglobinemia (7%–27% of Hb) in all age
groups, especially in the age group of less than one year (Gupta et al., 2000). Many studies have been
performed attempting to link stomach and gastrointestinal cancer to nitrate intake. Medical scientists claim
that nitrate represents a potential risk because of nitrosation reactions which, with appropriate substrates
present, form N-nitroso compounds which are strongly carcinogenic in animals (Forman, 1985). However,
Reactive Nitrogen in Agriculture, Industry and Environment in India 27

even at exposure to levels of 111mg l–1 there were no adverse conditions in infants except for
methaemoglobinemia (Gustafson, 1993). Recurrent stomatitis has also been found to be associated with
nitrates in drinking water (Gupta et al., 1999).
Adverse effects of nitrates in drinking water on animal health include methemoglobinemia in ruminants
and severe gastritis in monogastric animals, intestinal disorders in pigs, pregnancy related disorders in
rats, depression, muscle tremors and incoordination in goats, loss of body weight and reduced water
consumption in chickens, sexual disorders in sheep and hyperthyroid in foals (Prakasa Rao and Puttanna,
2000).

Extent of Nitrate Pollution of Groundwater Bodies in India

An appraisal of risk of nitrate pollution of ground water in different parts of India can be made by considering
together the fertilizer N use per unit area and extent of ground water development for irrigation purposes.
Excess nutrients in irrigation return flow, if not properly drained off, gradually infiltrate into aquifers. Using
the data generated by reconnaissance of nitrate content in shallow ground waters by Central Ground
Water Board (Handa, 1986), Agrawal (1999) categorized different states with respect to potential hazard
of nitrate pollution of ground waters (Table 17). With the highest ground water development, average
nitrate content in ground water and average fertilizer N use, the states of Punjab and Haryana have been
placed in the high risk zone. According to Agrawal (1999), irrigation without artificial drainage in the
poorly drained flat plains of Punjab and Haryana, comprising of a thick pile of unconsolidated and
permeable Late Quaternary-Holocene alluvial sediments (Lunkad, 1988), increases the nitrate pollution
hazard compared to that in the freely drained regions of northern and northeastern states and peninsular
plateau in the southern part of the country. Agriculture is not intensive in northern and northeastern
states as reflected in the meager consumption of nitrogenous fertilizers and negligible ground water use.
The situation in the peninsular states is in between the two extremes. Reports of ground water enrichment
with nitrate-N from different parts of the country are summarized below.
Northwestern India: Depending upon availability of irrigation water, the coarse textured soils in the
northwestern India are used for raising wheat as well as wetland rice. In this region there hardly occurs
any leaching of nitrate-N beyond the 2 m deep rooting zone of wheat crop (Katyal et al. 1987). On the
other hand, rice grown in summer receives around 150 cm irrigation besides 33 cm of average rainfall.
Under these conditions a large part of applied N is lost as nitrate via leaching to ground water. Interestingly,
due to high percolation rates, soil under rice experiences alternating aerobic-anaerobic cycles that facilitate

Table 17. Risk of ground water nitrate pollution in different parts of India

Risk zone Average fertilizer N Average NO3 in Ground water


consumption (kg ha-1) ground water development Region (states)
(mg l-1) (% of total
available in 1990)

Little or no risk 2 6-8 <2 Jammu and Kashmir, northeastern


states
Low risk 4-11 8-45 5-22 Himachal Pradesh, Madhya
Pradesh, Orissa, Maharashtra
Moderate risk 14-53 13-50 16-40 Uttar Pradesh, Uttranchal, Bihar,
Jharkhand, West Bengal, Andhra
Pradesh, Gujarat
High Risk 118-163 55-100 70-100 Punjab, Haryana
Source: Handa (1986), Agrawal (1999)
28 Bijay Singh, MK Tiwari and YP Abrol

production of nitrate unlike in ideal rice soils. Thus as described by Bijay-Singh et al. (2007) in detail,
nitrate N content in the ground water in Punjab have been consistently increasing since 1975 when first
sampling was made (Table 18). A significant correlation (r = 0.51*) was found to exist between the amount
of fertilizer N applied per unit area per year and nitrate N concentration of well water in September 1975.
Multiple correlation between well water nitrate N content and amount of fertilizer N applied in the vicinity
of the wells and depth to water-table was 0.53** in September and 0.39* in June 1975, suggesting thereby
that fertilizers may significantly increase nitrate N levels in the ground water in Punjab. As shown in
Table 18, the geometric mean of nitrate N content registered an increase from 0.42 to 2.29 mg l–1 during
1975 to 1988.
In 1992, ground water samples collected from 21 to 38 m deep tube wells located in cultivated
fields in different blocks of Punjab (fertilizer N use varying from 151 kg N ha–1 to 258 kg N ha–1) recorded
geometric mean nitrate N concentration of 3.62 mg l–1 (Table 19). Respectively, 78 and 22 % samples
contained less than 5 and 5–10 mg NO3––N l–1 (Bajwa et al., 1993). Higher nitrate N concentrations
in ground water were observed in areas under rice, maize and orchards. In contrast to cultivated area,
mean NO3––N concentration in 367 water samples collected from 9 to 18 m deep hand pumps located
in village habitations worked out to be 5.72 mg l–1 with 64 and 2 % samples containing 5–10 and >10
mg NO3––N l–1. In ground water samples collected from hand pumps located near animal feedlots or
dairy farms representing a concentrated source of animal wastes in the outskirts of villages, mean NO3–
–N concentration was observed to be 4.73+2.24 mg l–1. In 1999, several samples of water drawn from
shallow hand pumps contained nitrate-N levels much above the WHO limit of 10 mg N l–1 (Table 20).
Problem of ground water pollution by nitrates does not normally arise in areas where wetland rice
is grown on fine textured ideal rice soils because nitrate is not normally formed under flooded conditions.
Nitrate formed when soil is allowed to drain/dry may be promptly converted to nitrous oxide via

Table 18. Nitrate concentration (mg NO3-N l -1) in water samples from shallow wells (4 to 10 m deep) located
in agricultural land in Ludhiana district in Punjab during 1975 to 1988

1975 1982 1988


Jun Sep Jun Sep Nov / Dec
Number of observations 46 33 26 26 28
Range (mg NO3– – N1–1 ) 0.04-6.15 0.05-7.90 0.35-10.11 0.23-15.17 0.31-13.30
Geometric mean 0.42 0.42 1.48 2.13 2.29
(mg NO3– – N1–1 )
Correlation coefficient NS 0.51 NS 0.51 0.59
(r) fertilizer N
applied vs NO3 N in
well water
Significant at 5% level of significance
Source: Bijay-Singh et al. (1995)
*
Table 19. Nitrate concentration in water samples from tube wells in cultivated areas, hand pumps in village
habitations and beneath feedlots in rural areas in the Punjab

Type of well Number mg NO3-N l-1 Per cent samples having


of samples Mean Range <5 mg l -1 5-10 mg l -1 >10 mg l -1

Tube wells 236 3.62+1.52 1.00 – 6.72 78 72 0


Hand pumps 367 5.72+2.09 1.00 – 11.28 32 66 2
Feed lots 45 4.73+2.24 1.24 – 10.44 47 51 2
Source: Bajwa et al. (1993)
Reactive Nitrogen in Agriculture, Industry and Environment in India 29

Table 20. Nitrate-N content (mg N l–1) in tube wells and hand pumps located in agricultural land in the four
blocks of Ludhiana district in Punjab in July 1999

Block Tubewells Hand pumps


Range Mean Range Mean

High Fertilizer Use


Jagraon 2.46–16.16 6.49 3.57–49.74 12.60
Samrala 1.44–8.73 4.06 0.92-29.58 12.40
Low Fertilizer Use
Pakhowal 1.67–4.41 2.82 2.95–13.19 6.75
Dehlon 1.32–9.25 4.29 0.15–20.64 8.67
Mean values of nitrate-N in 1992 were: Tube wells = 3.62+1.52 (n = 236),
Hand pumps = 5.72 + 2.09 (n = 367)
Source: Bijay Singh et al. (1995), Roopna Kaur (2000)

denitrification. This is particularly true in case of typical or ideal rice soils, which possess very low percolation
rates after these are puddled.
Malik (2000) anlaysed data on nitrate content of ground water samples collected by the Punjab
and Haryana State Ground Water Boards. The number of observation wells in Punjab was 460 (including
72 pizometers) while that in Haryana it was 534 (including 164 pizometers). The results pertaining to
nitrate content of water samples in the two states are presented in Table 21. More than 33 % of the water
samples in Punjab and Haryana had nitrate level above the desired limit for drinking water standards.
In about 17 % of the samples, the nitrate-N level exceeded 22 mg l–1. Very high nitrate content of ground
water samples suggests that sources other than fertilizers can substantially contribute nitrates to ground
water.
Delhi: In many national capital sub-regions, ground water is severely polluted by nitrate. Most of these
regions are under agricultural land use. As low as 4.4 mg N l–1 to abnormally high levels (22.2–
228.8 mg N l–1) of nitrate in the ground water have been found at different places in the districts of
Rohtak, Sonepat, Faridabad and Gurgaon sub-region (Datta, 2005). Ground water of the national capital

Table 21. Nitrate concentration in ground waters of Punjab and Haryana

Nitrate concentration (mg NO3-N l -1) Number of samples Average nitrate level (mg NO3-N l -1)

Punjab
0 - 10 328 (69.8) 3.2
10 -22 71 (15.1) 14.8
>22 71 (15.1) 53.1
Total 470 (100.0) 12.5
Haryana
0 - 10 222 (63.1) 3.4
10 -22 62 (17.6) 15.2
>22 68 (19.3) 63.0
Total 352 (100.0) 19.0
Punjab and Haryana
0 - 10 550 (66.9) 3.3
10 -22 133 (16.2) 15.0
>22 139 (16.9) 58.0
Total 822 (100.0) 14.4
Source: Malik (2000)
30 Bijay Singh, MK Tiwari and YP Abrol

territory Delhi shows wide range in nitrate (2.2–355.5 mg N l–1) content. In 2003, nitrate levels in Delhi
ground water range from <0.22–30 mg N l–1 in Alipur Block; <0.22–35.3 mg N l–1 in Kanjhawala Block;
0.44–7.11 mg N l–1 in City Block; 0.44–159.1 mg N l–1 in Najafgarh Block; 4.22–67.3 mg N l–1 in Mehrauli
Block and 0.22–15.3 mg N l–1 in Shahdara Block. Large part of the area to the west, having very little
recharge from rainfall, is severely affected by nitrate pollution of ground water (Datta et al., 1997).
Domestic wastewater effluents in Delhi exhibit nitrate-N concentration ranging from 4 to
6.2 mg N l–1, which may be formed during aerobic treatment may also contribute to nitrate pollution
of ground water. However, lack of correlation between nitrate and chloride content reported by Datta
and Tyagi (1996) indicates that nitrate contribution from sewage is not significant in the whole area, except
for some specific locations. Ground water samples from the Indian Agricultural Research Institute farm
area showed non-uniform distribution of nitrate-N contents in most of the wells in 1990, 1991, 1995,
2000, 2002 and 2003 (Datta, 2005). Analyses of soil cores indicated downward movement of two different
nitrate peaks up to 1.8 m and 5.8 m depth below ground level. This suggests that nitrate-N is moving
down in pulses. The relationship between NO3 and ä18O also suggests that the ground water in Delhi
originates from two or more isotopically distinct, non-point sources which vary spatially as well as
temporarily, due to different degrees of evaporation/recharge (Datta et al., 1996, 1997) and different
amounts of fertilizer N applied.
Uttar Pradesh and Bihar: The range of concentration of nitrate-N in ground waters around Lucknow
is 10–130 mg l–1 (Sehgal et al., 1989). Similarly in Barauni (Bihar), Mishra et al. (2000) has reported
nitrate levels in ground water samples higher than the maximum permissible limit of 10 mg l–1. About
7500 km2 of the upper Yamuna basin has been classified as an area sensitive to nutrient and contaminant
leaching (Narula et al., 2003).
Maharashtra: The studies carried out by the Central Ground Water Board in the state of Maharashtra
revealed that out of 688 samples, 75 % of the samples had nitrate levels below the critical limit, 14 %
have nitrate levels above 22.2 mg N l–1. While the districts of Bhandara, Nagpur and Pune showed nitrate
concentrations of above 10 mg N l–1, Jalna district had the highest percentage of samples (55.56 %)
with nitrate concentrations above the permissible limits. Districts like Akola, Amravati, Chandrapur,
Sholapur, Wardha, Yavatmal have nitrate concentrations above 22.2 mg N l–1. In studies carried out by
Deshpande et al. (1999), ample evidence for nitrate pollution of ground water in Aurangabad district
of Maharashtra has been obtained.
South India: A study of ground water quality in Karnataka during 2000–2001 indicated 37% of habitations
(numbering 20,929) are facing water quality problems and nitrate was a problem in 4,077 habitations
(Nagaraj and Chandrashekaran, 2005). In the extensive GIS based survey based on 154,491 samples,
nitrate-N content ranged from 22.4 to 1347.5 mg N l–1. A large number of villages were found to be
affected by high nitrate content in drinking water and pose a serious health problem. The relative number
of villages affected is given in parenthesis for some of the worst affected districts: Tumkur (35%), Mysore
(20%), Kolar (21%), Raichur (10%), Mandya (5%), Devanagere (15%), Chamarajanagara (14%), Chitradurga
(15%). These data suggest the presence of nitrate bearing rocks in geological formations as in some parts
of Haryana. About 48% of the bore well waters of Mysore city contained more than 10 mg N l–1 of nitrate
(Nagaraju and Sastri, 1999).
In Andhra Pradesh, wherever fertilizer applications are high, there is ample evidence of pollution
of ground waters by nitrate-N (Srinivasarao, 1998). Even in semi-arid regions of Deccan plateau nitrate
leaching was prevalent (Patra and Rego, 1997). In Palar and Cheyyar river basin in Tamil Nadu, spatial
Reactive Nitrogen in Agriculture, Industry and Environment in India 31

and seasonal variations have been analysed and relationship has been found between agricultural activities
and nutrient chemistry of well water (Rajmohan and Elango, 2005). Nitrate content, however, was found
to be within WHO drinking water limits. In Chennai, nitrate-N levels in ground waters have been reported
in the range of 3 to 226 mg N l–1 (Rangarajan et al., 1996). Ground water samples in Swaminathapuram,
Dindgal district, Tamil Nadu have been found to contain 1.4–3.8 mg N l–1 nitrate (Thirumathal and
Shivakumar, 2003).

Sources of Nitrates in Groundwater other than Fertilizers

Although there has been a concurrent rise in fertilizer usage with nitrate-N concentration in water, particularly
where irrigation is practiced, there exist several other sources of nitrate-N, namely sewage effluent, animal
excreta, natural soil nitrate and decomposition of soil organic matter. In many regions, natural deposits
of nitrate may constitute a major source for nitrate pollution of ground water. For example, in selected
locations in Punjab, Haryana and western Uttar Pradesh, nitrate-N concentration in well water samples
was several folds higher than the upper safe limit (Table 22).
Given that there are no major geological deposits in the central Punjab where fertilizer N application
rates are the highest in the state, area and major water polluting industries are few, major source of nitrate
in ground water could either be sewage and animal wastes and/or agricultural chemicals – particularly
N fertilizers. The area is densely populated and raw or inadequately treated sewage is either discharged
into irrigation channels or quite often discharged into pits or depressions from where the pollutants could
percolate down into the ground water. The region also has a high density of cattle population. A close
scrutiny of the available data revealed that there is no discernible pattern of distribution of nitrates in
ground waters of Punjab and Haryana (Malik, 2000). At some places where high nitrate levels in ground
water have been detected, there is a sharp decrease in nitrate-N concentration a short distance away
and vice versa. Such sudden changes in nitrate levels in ground water indicate that there is no regular
pattern of nitrate distribution and pollution is localized. Thus, sewage disposal along with leaching of
fertilizer N are contributing to the nitrate pollution of the ground water in the Punjab. The extent of
contribution of each source is, however, difficult to evaluate.
In a study undertaken by National Environmental Engineering Research Institute (Bulusu and Pande,
1990), 1290 out of 4696 (27 %) ground water samples from selected districts in 17 states in India (excluding
northeastern states) contained more than 10 mg N l–1, the WHO upper limit. High nitrate levels in 73%
samples from Nagpur metropolitan should be due to urban sewage and industrial sources. Similarly high
nitrate-N content (10 to >133.3 mg l–1) in shallow and deep tube wells due to seepage from industrial
effluents and urban sewage has been reported from around Jodhpur city in Rajasthan (Mathur and
Ranganathan, 1990) and Lucknow in Uttar Pradesh (Singh et al., 1991).

Table 22. Nitrate content of well waters in Uttar Pradesh, Haryana and Punjab

State District mg NO3--N l -1 State District mg NO3--N l -1 in well


in well water water

Uttar Pradesh Aligarh 61 Haryana Mahendragarh 296


Meerut 157 Ambala 223
Agra 54 Punjab Hisar 95
Bathinda 128
Sangrur 98
Source: Handa (1987)
32 Bijay Singh, MK Tiwari and YP Abrol

NITROGEN IN RIVERS, COASTAL ECOSYSTEMS AND OCEANS

In coastal ecosystems, such as in estuaries and shallow embayments, sediments play a key role in the
cycling of nutrients to and from the water column. These coastal areas are important because of their
role as transient zones between land and sea in their capacity of retaining nutrients; they also harbor
a great variety of benthic primary producers, such as sea grasses, macroalgal mats and microphytobenthic
communities, which live in the sediment. Reactive N in coastal ecosystems is generally received through
riverine and groundwater inputs. In some cases direct atmospheric deposition inputs from the ocean can
also be important. These inputs have increased several-fold as a consequence of human activities. Because
of the dynamic nature of coastal ecosystems, there is limited potential for reactive N accumulation (Galloway
et al., 2003). Due to high rates of denitrification (mostly as N2) the reactive N reaching coastal regions
is mostly converted to N2 before its transport to the open ocean. With coastal systems acting as reactive
N sinks, atmospheric deposition becomes a potentially important source of reactive N for the open ocean.
Although reactive N has a short residence time in coastal ecosystems, it can still have a profound impact
on the coastal ecosystem because primary production in most coastal rivers, bays, and seas of the temperate
zone is limited by reactive N supplies (Vitousek and Howarth 1991, Nixon et al. 1996). Greater reactive
N inputs lead to increased growth of algae.
In the Asian nitrogen cycle case study conducted by Zheng et al. (2002), the riverine discharge of
dissolved inorganic nitrogen derived from anthropogenic reactive N in Asia into the Pacific and Indian
Oceans was estimated at ~ 2.6 Tg N year–1 in 1961, ~ 6.8 Tg N year–1 in 2000 and ~ 9.6 Tg
N year–1 in 2030. The discharge rates around 2000 accounted for approximately 34% of the global total
of ~ 20 Tg N year–1 (Seitzinger and Kroeze, 1998). The estimated rate of this study for mid 1990s
(~ 6.4 Tg N year–1) is lower than that (~ 9 Tg N yr–1) presented by Seitzinger and Kroeze (1998). National-
level analysis showed that ~ 66% of the Asian total dissolved inorganic nitrogen discharge by rivers occurs
in China and India. According to Caraco and Cole (1999), reactive N is being exported in the form of
nitrates out of the watershed of the Ganges, Yangtze, Huanghe and Mekong at a rate of 601, 495, 276
and 144 kg N year–1 km–2, respectively. Nearly 2,236 Mg of nitrogen is discharged into Mahim Bay alone
every year from various sources (Sen Gupta et al. 1989). This may even lead to phytoplankton blooms
in coastal areas and carbon and energy become concentrated at lower tropic levels with potentially significant
effects for ecosystem structure and function. These marine regions where phytoplankton blooms occur
are located adjacent to rapidly developing agricultural areas in South Asia (Beman et al., 2005).
Nearly all the reactive N that is injected into surface waters is denitrified along the stream–river–
estuary–ocean continuum (Galloway et al., 2003). While most of this reactive N is converted to N2, a
fraction is converted to N2O and NO. Model estimates suggest that rivers, estuaries, and continental shelves
account for approximately 30% of the total global anthropogenic N2O emissions (Seitzinger et al., 2000).
In a recent study in the Andaman Islands (Barnes et al., 2006), denitrification rates as reported in
Table 23 were generally up to 3 orders of magnitude lower than in typical temperate settings (Barnes

Table 23. Denitrification rates in four Indian mangroves

Area Rate of denitrification (mmol m-2 h-1)

Andaman Islands, India 7.6


Muthupet, South India 17.4
Pichavaram, South India 23.0
Sunderbans, India 11.2
Source: Barnes et al. (2006)
Reactive Nitrogen in Agriculture, Industry and Environment in India 33

and Owens, 1998), consistent with low concentrations of NO3– in the mangrove surrounding waters. The
N2O emission fluxes were relatively high (0.5–10.4 ìmol m–2 d–1) and in good agreement with other studies
of mangroves N2O emissions (Bauza et al., 2002; Corredor et al., 1999). The studies carried out by Corredor
et al. (1999) and Bauza et al. (2002) implied that nitrification was the major N2O source; the estimated
N2O emissions generally far exceed the reported maximum denitrification N2O yield of 6% (Nevison and
Holland, 1997). Given that the energy yield for organic C oxidation by reduction of N2O to N2 is high
(second only to that of aerobic respiration) in most mangrove sediments, denitrification is likely to be
a sink for N2O rather than a source (Amritha et al., 2007).
The Arabian Sea is vulnerable to potential environmental and climatic changes arising from human
activities including rapid population growth, intensification of agricultural activities including large increases
in the consumption of nitrogen fertilizers, industrialization, and urbanization of coastal zones in the major
littoral countries (India, Pakistan and Iran) (Bange et al., 2005). Bange et al. (2000) estimate that
~1.2 Tg of N in the dissolved inorganic form is added annually to the Arabian Sea (Table 24); this input
represents about 29% of the total fixed-N in annual river runoff from South Asia (4.2 Tg inorganic N;
Seitzinger et al., 2002). Due to lack of systematic, long-term investigations of biogeochemical cycles, it
is difficult to evaluate the extent to which human activities have affected the biogeochemical processes
of the Arabian Sea (Bange et al. 2005). The most convincing evidence in this regard comes from the
eastern Arabian Sea where coastal waters seem to have undergone a dramatic change during the last
few years indicated by the shift from seasonally low-O2 conditions (Banse, 1959; Carruthers et al., 1959)
to suboxic and even anoxic conditions (Naqvi et al., 2000). The most intriguing aspect of N cycling in
the coastal O2-deficient zone is the enormous accumulation of N2O. It seems to occur in waters experiencing
intense and relatively short-lived denitrification, a pattern that distinguishes the coastal suboxic system
from the one located offshore (Naqvi et al., 2005). Depletion of O2 in coastal waters will not only lead
to increased emissions of greenhouse gases such as N2O but will also change the food web structure
and fisheries (Malakoff, 1998; Wu, 2002). Annual input of N by wet and dry aerosol deposition is estimated
to be about 1.6 Tg N and represents a minor source of N for the Arabian Sea (Bange et al., 2000).
However, as is the case for land runoff, the atmospheric inputs of N through both dry and wet deposition
are expected to increase steadily. During the north-eastern monsoon, air masses from the Indian subcontinent

Table 24. Nitrogen budget of Arabian Sea (north of 6° N)

Tg N year-1

Sources
Atmospheric dry and wet deposition of NO3 and NH4 1.6
Pelagic N fixation 3.3
Input from marginal seas (red Sea, Persian Gulf) 1.1a
Dissolve inorganic N input from rivers 1.2b
Northward transport 38
Sinks
Pelagic denitrification 33
Sedimentary denitrification 6.8
N sedimentation >0.22
N2O loss to the atmosphere 0.25
NH3 loss to the atmosphere 0.05c
Ó Sources – Ó Sinks 4.9
Source: Bange et al. (2000)
34 Bijay Singh, MK Tiwari and YP Abrol

are transported to the central Arabian Sea where the NH4+ and NO3– containing aerosols that originate
from agriculture and combustion processes fertilize the N-depleted surface waters. Bange et al. (2000)
estimated that up to 17% of the N demand in the surface layer of the central Arabian Sea during the
north-eastern monsoon is being met by the deposition of nitrogenous aerosols. Assuming that the amount
of N aerosols will increase in the future, this source can have impacts on both biogeochemical cycling
and ecosystem structure.

CHALLENGES AND OPTIONS FOR MITIGATION OF ENVIRONMENTALLY IMPORTANT


REACTIVE NITROGEN, RESEARCH AND PLANNING

The International Nitrogen Initiative – a global effort to optimize nitrogen’s beneficial role in sustainable
food production and to minimize nitrogen’s effect on human health and the environment aims at pursuing
a three stage strategy that involves assessing knowledge on N flows and associated problems, developing
region specific solutions and implementing scientific, engineering and policy tools. The development of
policies to control unwanted reactive N release is not easy because the largest amount of anthropogenically
fixed reactive N is related to food and energy production and reactive N species can be transported great
distances in the atmosphere and in aquatic systems. Reactive N emissions from fuel combustion (NOx)
can be reduced by following strict policies but reducing the introduction of new reactive N in food production
seems to be very difficult in countries like India having burgeoning populations. Food production still
needs to be increased to raise nutritional levels or to keep up with population growth, which may require
increased use of N fertilizers. Nevertheless, policies are to be implemented and enforced at the national
or provincial/state levels although N cycling occurs at regional and global scales. Multinational efforts to
control N loss to the environment are surely needed, but these efforts will require commitments from
individual countries and the policy-makers within those countries (Mosier et al. 2002).
Fertilizer nitrogen use has been an essential component of the Green Revolution that dramatically
increased food production in India during the period between 1960 and 1980. Fertilizer use will continue
to grow as food production does, in order to keep pace with a still-rapidly increasing human population.
Use of N for agriculture, whether in the form of synthetic or organic fertilizer, is not substitutable, and
straightforward technological changes are unlikely to provide a replacement. Plants will always require
a relatively large amount of N to carry out their photosynthetic processes, and one key to maintaining
adequate food supplies will be supplying plants with adequate N (Matson et al. 1997). As a matter of
fact, the loss of fertility of agricultural soils as a result of depletion of nitrogen can lead to reduced food
production resulting in a catastrophe no less serious than from other forms of environmental degradation.
Thus benefits of fertilizer use to agricultural production in India far outweigh the detrimental effects on
the environment. Use of increasing amounts of reactive N in the form of fertilizers in Indian agriculture
and the proper management of fertilizer N will remain at the forefront of issues to improve the reactive
N balance over both the short- and long-term. To achieve the tripartite goal of food security, agricultural
profitability and environmental quality in a country like India, improving N use efficiency in agriculture
will have to be the top priority. Since practices that result in high fertilizer nitrogen use efficiency provide
environmental protection, high crop yields and profits, increasing fertilizer use efficiency should be among
the highest research priorities. Holistic approach to farming systems will have to be adopted and it should
be based on soil characteristics, climatic constraints, moisture availability and the management skills of
the individual farmers. Other important research areas that can help improve fertilizer use efficiency are
integrated management of organic, biological and mineral nutrient sources, identification of best management
practices and fertilizers for specific conditions. Some other ways to increase the efficiency of reactive N
use in food production and thus decrease the reactive N creation rate can be to increase recycling of
reactive N within agroecosystems (Smil 2002), increase use of cultivation- induced BNF (Roy et al. 2002),
Reactive Nitrogen in Agriculture, Industry and Environment in India 35

provide incentives to reduce over fertilization, and redistribute reactive N from areas with high reactive
N production to areas where there is a need for reactive N for food production (Galloway et al., 2003).
Innovative fertilizer management has to integrate both preventive and field specific corrective N
management strategies to increase the profitability in irrigated rice and wheat systems and to ensure that
there exists synchrony between crop N demand and supply of mineral N from soil reserves and fertilizer
inputs. It will lead to maintenance of plant available N pool at the minimum size required to meet crop
N requirements at each growth stage with little vulnerability to loss of N to environment. There is significant
potential to increase N use efficiency at the farm level because concepts and tools needed to achieve
it are already available. However, new technologies need to be cost effective and user-friendly so that
these become attractive to farmers. Collaborative effort of agronomists, soil scientists, agricultural economists,
sociologists, ecologists and politicians can help agriculture make substantial contribution to reduce the
reactive N load.
The need to identify relative contribution of fertilizer N to environmental problems on a regional
basis is very important. For example, in some regions, inputs other than fertilizers, such as animal wastes,
may be main polluter. To work out precisely the contribution of fertilizers to nitrate pollution of ground
water, there is a need to monitor periodically nitrate-N status of ground water at different depths and
monitoring the changes every 2-3 years. It will also help distinguish different sources of nitrate-N and
their contributions to ground water pollution. Comprehensive models which can predict the amount of
N reaching the natural water bodies under the given set of soil, crop and climatic conditions are needed
to be developed. Calculation of residence time of nitrate-N in the soil profile after it escapes the root
zone will enable prediction of time trends for nitrate-N levels in ground water bodies. Methods of controlling
leaching losses of nitrates from agricultural fields through better cropping practices, better fertilizer
management and better irrigation management need to be further refined. Non-availability of comprehensive
data sets in India is a major problem in detection and prevention of nitrate pollution of ground water.
Central Pollution Control Board and Central Ground Water Board of India are engaged in monitoring
of water quality in the country but still the extent and distribution of pollutants across the country has
not been quantified. Therefore, it is essential to establish ground water-monitoring stations through out
the country. The pollution from industrial effluents/sewage has already gripped many industrially developed
cities that this aspect needs special attention. In order to make appropriate and efficient plans and strategies
to combat the menace of the nitrate pollution of ground water, concentrated research efforts are necessary
to generate information related to the status of pollution, its nature and possible impacts on the system.
Since it impossible to have too many field studies, models must be modified and/or developed through
intensive detailed field investigations and validated for a diverse set of conditions. It will enable extrapolating
the results to other locations. At present, there is scarcity of both under the Indian context.
There is no benefit of the reactive N created during fossil fuel combustion because NOx are formed
during combustion either through oxidation of fossil-organic reactive N in the fuel or through oxidation
of atmospheric N2. There can be several options for significantly reducing NOx emissions. Using an
alternative method to provide energy or by eliminating NOx and other reactive N species from the
combustion products are possible (Bradley and Jones 2002, Moomaw 2002). It is now technically feasible
to decrease reactive N creation from fossil fuel combustion to a point where it becomes just a minor
disturbance to the reactive N cycle (Galloway et al., 2003).
Efforts to improve energy efficiency, measured in terms of the services obtained per unit of fuel
consumption, will be a major focus of environmental policy in India because anthropogenic emissions
of NOx are dominated by fossil fuel combustion. Change in the N cycle through emissions of NOx in
36 Bijay Singh, MK Tiwari and YP Abrol

India as linked to the use of fossil fuel energy are likely to increase dramatically over the next several
decades, unless there is a concerted effort to control fossil fuel consumption. Technological changes that
either increases efficiency of fuel combustion or removes nitrogen oxides from the exhaust stream should
be able to reduce the total amount of N emitted, but complete solutions are closely linked to the development
of non-polluting alternative energy sources.
Assessment of various N pools, N-cycling and N mass balance studies on all geographical and time
scales are characterized by high variability and uncertainty. The data sources, models/methods adopted,
change in cropping pattern, biomass burning, environmental and climatic factors introduces variability
in the measurements at different levels and extend. Since N2O emission from soils is a key source of
N containing green house gases emissions in India, it is necessary to develop appropriate emission
coefficients through measurements covering the different seasons in the diverse cropping systems of the
country. Thus it is important essential to properly understand different kinds of N fluxes and to quantify
variations in inputs and losses as ranges rather than as single values.
Human impacts on the N cycle strongly depend upon the rates at which fixed N is denitrified to
N2 in land and aquatic systems. Unfortunately, a quantitative understanding of denitrification rates in
various managed and unmanaged terrestrial and aquatic environment is largely missing. This is probably
the biggest obstacle in accurate modeling of the N cycle. In addition to this, in India, climatic conditions
(air and soil temperature, precipitation, wind and relative humidity) vary with seasons and strongly influence
fluxes of N2O emissions and NH3 volatilization. Accurate estimates can be obtained by means of model
simulations in conjunction with observations at large scales and linking of point measurements to spatial
data sets.

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ABOUT THE BOOK

The current status of reactive nitrogen which consists of all biologically, chemically and radiatively active nitrogen
compounds in terrestrial, coastal and atmospheric realms and development of technologies to minimize nitrogen In Agriculture, Industry and Environment in India
impacts on the environment needs to be addressed in the right perspective. The development of policy to control
unwanted reactive N release in the environment is difficult because much of the reactive N release is related
to food and energy production and reactive N species can be transported great distances in the atmosphere
• Bijay Singh • Mithilesh K. Tiwari • Yash P. Abrol
and in aquatic systems.
This publication is an outcome of the activities of the Indian Nitrogen Group, a national network of scientists
concerned with issues related to reactive nitrogen. It presents an overview of reactive nitrogen in agriculture,
industry and environment in India. Since reliable quantitative information about several aspects of reactive
nitrogen in the country is not yet available, it should prove very valuable for the scientific community in terms
of initiating projects to fill the gaps. It should also help planners in agriculture, industry and energy production
to guide future expansion in the economy in a way that the delicate balance between inputs and outputs of
reactive nitrogen in the environment is maintained.

ABOUT THE AUTHORS


Professor Bijay Singh, ICAR Dr. Mithilesh K. Tiwari is Director of Professor Yash P Abrol, formerly Head
National Professor, has been working the South Asian Regional Centre of the of the Division of Plant Physiology at
on different aspects of nitrogen in International START Programme that is the Indian Agricultural Research Precipitation

rice-wheat cropping system for more responsible for nurturing regional Institute, New Delhi, subsequent to
than two decades. His contributions cooperation for studies on Global serving as CSIR Emeritus Scientist and Gaseous Losses

Organic Residues
on nitrogen balance in soil-plant Change with particular emphasis now INSA Senior Scientist (1996-2001; 2001- Denitrification
Plant Consumption
Organic Matter

systems have lead to better on Climate Change Adaptation. He 2005), is at present associated with the Nitrates Nitrification
Mineralization
Ammonium
through bacteria

heads the Centre on Global Change Department of Environmental Botany, Fixation

understanding for (i) enhancing Leaching Nitrites Clay Minerals

Project of CSIR and the Radio and Hamdard University, New Delhi as
nitrogen use efficiency in rice-wheat
Adjunct Professor and INSA Honorary Jammu & Seagull
cropping system (ii) fertilizer nitrogen Atmospheric Sciences Division, Kashmir Atmospheric N2

Scientist,. He has immensely contributed Himachal


related environmental pollution, and National Physical Laboratory at New Pradesh
Wetland
to nitrogen research and has published Punjab Uttaranchal Vegetation
(iii) integrated nutrient management. Delhi. He is an active Core Team DELHI
Arunachal
Pradesh Oceans
profusely in reputed journals. He is Uttar
Sikkim
Assam
containing
CO(NH2)2
He is a fellow of Indian National Member of the Indian Nitrogen Group. actively involved in organizing INDIAN
Rajasthan Pradesh
Bihar Megalaya
Nagaland
Manipur
Tripura
He has extensively contributed to the

Jh a
Science Academy, National Academy Gujarat West Mizoram

r kh
NITROGEN GROUP under the aegis of Madhya Pradesh Bengal

and
rh
ga Decaying
of Agricultural Sciences and Indian growth of several major national level the Society for Conservation of Nature. Ch
ttis
ha Orissa
Kolkata
(Calcutta) Nitrogen fixing
dead animal
Mumbai Maharashtra soil bacteria
Society of Soil Science. He is decorated research programmes in space sciences. He is a Fellow of the INSA, Indian
(Bombay) Denitrification
by denitrifying
bacteria
Andhra

with several awards notably the Rafi His research interests are atmospheric Academy of Sciences, National Academy Goa a tak
a Pradesh
Ammonification
Decomposition
(Bacteria and
K ar n fungi)

Ahmad Kidwai Memorial Prize of environmental change processes and of Sciences and NAAS. He received Lakshdeep Chennai (Madras)
(NH4+) Ammonium (NH4+)
Open Water

ICAR. He is continuing work on impacts. Currently member of INSA’s several awards notably ICAR National Tamil
Kerala Nadu
Andaman & Nicobar
Assimilation
Nitrification by
nitrifying
Nitrification by
nitrifying bacteria
Nitrogen bacteria

increasing fertilizer nitrogen use National Committee for SCAR, he also Fellowship, FAI Dhirubhai Morarji (NO2) Nitrites
(NO2)

efficiency in rice and wheat at Punjab served the National Committees for IGBP Memorial, R.D. Asana, Sukumar Basu,
Agricultural University, Ludhiana. and COSPAR. VASVIK and FICCI awards.

INDIAN NATIONAL SCIENCE ACADEMY


Bahadur Shah Zafar Marg, New Delhi-110002

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