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 ABATEMENT OF
ENVIRONMENTAL
POLLUTANTS
TRENDS AND STRATEGIES

Edited by

PARDEEP SINGH
AJAY KUMAR
ANWESHA BORTHAKUR
Elsevier
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 Contributors
Mohd Aamir Center of Advanced Study in
Botany, Institute of Science, Banaras Hindu
University, Varanasi, India
Arif Ahamad School of Environmental Sciences
(SES), Jawaharlal Nehru University, New
Delhi, India
Assel I. Akhmetova Advanced Technologies
Center, Moscow, Russian Federation
Rahul Bhadouria Department of Botany, Insti-
tute of Science, Banaras Hindu University,
Varanasi, India; Department of Botany, Uni-
versity of Delhi, Delhi, India
A.K. Bhatiya Department of Biotechnology,
GLA University, Mathura, India
Muhammad Bilal College of Biotechnology,
Tianjin University of Science and Technology,
Tianjin, China
Preetismita Borah CSIR-Central Scientific
Instruments Organisation, Chandigarh, India
Anwesha Borthakur Leuven International and
European Studies (LINES), Katholieke Uni-
versiteit Leuven, Belgium
Antra Chatterjee Molecular Biology Section,
Centre for Advanced Study in Botany,
Department of Botany, Banaras Hindu
University, Varanasi, India
Mohd Ashraf Dar Department of Environ-
mental Science, School of Earth Sciences, Cen-
tral University of Rajasthan, Ajmer, Rajasthan,
India
Pooja Devi CSIR-Central Scientific Instruments
Organisation, Chandigarh, India
Rajkumari Sanayaima Devi Deen Dayal
Upadhyaya College (University of Delhi), New
Delhi, India
Akanksha Gupta Institute of Environment &
Sustainable Development, Banaras Hindu
University, Varanasi, India
ix
Shalini Gupta School of Environment and Sus-
tainable Development, Central University of
Gujarat, Gandhinagar, India
Deepak Gupta Institute of Environment &
Sustainable Development, Banaras Hindu
University, Varanasi, India
Garima Kaushik Department of Environmental
Science, School of Earth Sciences, Central Uni-
versity of Rajasthan, Ajmer, Rajasthan, India
Razia Khan Department of Microbiology, Gir-
ish Raval College of Science, Gujarat Univer-
sity, Gandhinagar, India
Zeenat Khan Environmental Genomics and
Proteomics Lab, BRD School of Biosciences,
Satellite Campus, Sardar Patel University,
Vallabh Vidyanagar, India
Arvind Kumar State Key Laboratory of Cotton
Biology, Key Laboratory of Plant Stress Biol-
ogy, School of Life Science, Henan University,
Kaifeng, Henan, PR China
Ajay Kumar Agriculture Research Organization
(ARO), Volcani Center, Rishon LeZion, Israel
Cash Kumar Cytogenetics Laboratory, Depart-
ment of Zoology, Institute of Science, Banaras
Hindu University, Varanasi, India
Manish Kumar CSIR-Central Scientific In-
struments Organisation, Chandigarh, India
Arun Kumar Bihar Agricultural University,
Sabour, Bhagalpur, India
Sughosh Madhav School of Environmental
Sciences (SES), Jawaharlal Nehru University,
New Delhi, India
P.K. Mishra Department of Chemical Engi-
neering and Technology, Indian Institute of
Technology (Banaras Hindu University), Vara-
nasi, India
x CONTRIBUTORS
Virendra Kumar Mishra Institute of Environ-
ment & Sustainable Development, Banaras
Hindu University, Varanasi, India
Arpan Modi Agriculture Research Organiza-
tion, Ministry of Agriculture and Rural Devel-
opment Volcani Centre, Rishon LeZion, Israel
Dan Bahadur Pal Department of Chemical
Engineering, Birla Institute of Technology,
Mesra, Ranchi, India
Shilpi Pandey Department of Botany, Institute
of Science, Banaras Hindu University, Vara-
nasi, India
Amit Kumar Patel Institute of Environment &
Sustainable Development, Banaras Hindu
University, Varanasi, India
Vipul Patel Environment Management Group,
Center for Environment Education, Ahmeda-
bad, India
Bhawana Pathak School of Environment and
Sustainable Development, Central University
of Gujarat, Gandhinagar, India
Deepak Pathania Department of Environmental
Sciences, Central University of Jammu, District
Samba, India
Priyanka Cytogenetics Laboratory, Department
of Zoology, Institute of Science, Banaras Hindu
University, Varanasi, India
Bhadouria Rahul Department of Botany,
University of Delhi, New Delhi, India
Archana Rai Department of Molecular and
Cellular Biology, Sam Higginbotom Institute
of Agriculture, Technology and Sciences
(SHIATS), Allahabad, India
Amit Ranjan Department of Kayachikitsa
Institute of Medical Sciences, Banaras Hindu
University, Varanasi, India
Divya Singh Center of Advanced Study in
Botany, Institute of Science, Banaras Hindu
University, Varanasi, India
Pardeep Singh Department of Environmental
Science, PGDAV College, University of Delhi,
New Delhi, India
Rajesh Kumar Singh Department of Dravya-
guna, Institute of Medical Sciences, Banaras
Hindu University, Varanasi, India
Tripti Singh Department of Biotechnology, GLA
University, Mathura, India; Department of
Chemical Engineering and Technology, Indian
Institute of Technology (Banaras Hindu Uni-
versity), Varanasi, India
Sandeep Kumar Singh Center of Advanced
Study in Botany, Institute of Science, Banaras
Hindu University, Varanasi, India
Vipin Kumar Singh Center of Advanced Study
in Botany, Institute of Science, Banaras Hindu
University, Varanasi, India
Manoj Kumar Singh Department of Chemistry,
Indian Institute of Technology Delhi, Hauz-
khas, India
Rishikesh Singh Institute of Environment &
Sustainable Development, Banaras Hindu
University, Varanasi, India
Gurudatta Singh Institute of Environment &
Sustainable Development, Banaras Hindu
University, Varanasi, India
Raghwendra Singh Crop Production Division,
ICAR-Indian Institute of Vegetable Research,
Varanasi, India
Prashant Kumar Singh Agriculture Research
Organization, Ministry of Agriculture and Ru-
ral Development Volcani Centre, Rishon
LeZion, Israel
Pratap Srivastava Department of Botany, Insti-
tute of Science, Banaras Hindu University,
Varanasi, India; Shyama Prasad Mukherjee
Government Degree College, Phaphamau,
Prayagraj, India
Akhileshwar Kumar Srivastava The National
Institute for Biotechnology in the Negev, Ben-
Gurion University of the Negev, Beer-Sheva,
Israel
Neha Srivastava Department of Chemical
Engineering and Technology, Indian Institute
of Technology (Banaras Hindu University),
Varanasi, India
 CONTRIBUTORS
Manita Thakur Department of Chemistry,
Maharishi Markandeshwar University, Solan,
India
Kangming Tian Department of Biological
Chemical Engineering, College of Chemical
Engineering and Materials Science, Tianjin
University of Science and Technology, Tianjin,
China
Dhanesh Tiwary Department of Chemistry,
Indian Institute of Technology (IIT-BHU),
Varanasi, India
Sachchidanand Tripathi Deen Dayal Upad-
hyaya College (University of Delhi), New
Delhi, India
Ruchita Tripathi Department of Dravyaguna,
Institute of Medical Sciences, Banaras Hindu
University, Varanasi, India
xi
Juan Francisco Villareal Chiu Universidad
Autónoma de Nuevo León, Facultad de Cien-
cias Químicas, Laboratorio de Biotecnología.
Av. Universidad S/N Ciudad Universitaria,
San Nicolás de los Garza, Nuevo León, Mexico
Wang Wenjing State Key Laboratory of Cotton
Biology, Henan Key Laboratory of Plant Stress
Biology, School of Life Science, Henan Univer-
sity, Kaifeng, Henan, China
Deepanker Yadav Department of Vegetable
and Fruit Science, Institute of Plant Science,
Agriculture Research Organization (ARO), The
Volcani Center, Rishon LeZion, Israel
Igor V. Yaminsky Lomonosov Moscow State
University, Moscow, Russian Federation
 C H A P T E R

1
Bioremediation: a sustainable
approach for management of
environmental contaminants
Pardeep Singh1, Vipin Kumar Singh2, Rishikesh Singh3,
Anwesha Borthakur4, Sughosh Madhav5, Arif Ahamad5,
Ajay Kumar6, Dan Bahadur Pal7, Dhanesh Tiwary8,
P.K. Mishra9
1
Department of Environmental Science, PGDAV College, University of Delhi, New Delhi,
India; 2Center of Advanced Study in Botany, Institute of Science, Banaras Hindu University,
Varanasi, India; 3Institute of Environment & Sustainable Development, Banaras Hindu
University, Varanasi, India; 4Leuven International and European Studies (LINES), Katholieke
Universiteit Leuven, Belgium; 5School of Environmental Sciences (SES), Jawaharlal Nehru
University, New Delhi, India; 6Agriculture Research Organization (ARO), Volcani Center,
Rishon LeZion, Israel; 7Department of Chemical Engineering, Birla Institute of Technology,
Mesra, Ranchi, India; 8Department of Chemistry, Indian Institute of Technology (IIT-BHU),
Varanasi, India; 9Department of Chemical Engineering and Technology, Indian Institute of
Technology (Banaras Hindu University), Varanasi, India

1. Introduction
Polluted soil resulting from industrial or agricultural processes poses serious health
hazards to humans and animals and thus can have damaging consequences on the
ecosystems by making land inappropriate for cultivation and other fiscal purposes. Various
industries such as carpet, textile, and petrochemical production create intensive problems in
the natural environment by disposing toxic wastes on one hand and generating a huge quan-
tity of waste, oily sludge, and petroleum waste enriched soil on the other hand, which
constitutes a major confront for hazardous waste management (Farhadian et al., 2008).

Abatement of Environmental Pollutants

https://doi.org/10.1016/B978-0-12-818095-2.00001-1 1 Copyright © 2020 Elsevier Inc. All rights reserved.
2 1. Bioremediation: a sustainable approach for management of environmental contaminants

Apart from this, oil shipping is also one of the key causes of environmental contamination
where the land and water gets polluted because of the oil spill, ship breakage, and seepage
of oil pipelines.
The economically viable and environmentally feasible management of industrial sludge is
a major concern worldwide. For disposal of industrial sludge, globally adopted technologies
comprise of landfilling, high-temperature drying, sludge spreading on land surface,
lime added stabilization, burning, and composting. Because of excessive expenditure on
sludge management, the majority of textile industries in India generally released their
wastewater effluents in the farming fields, open dumps, fallow land, and ineffectively
controlled sanitary landfills and alongside the railway tracks. It further contaminates ground-
water causing serious human health hazards. Meanwhile, low availability of landfill area,
rigorous national wastes discarding policy, and local people awareness have caused landfill-
ing and land spreading highly costly and impractical. The sludge management practices
in most of the developing countries are not well developed. Currently, several factories
and municipalities are working on environment-friendly and low-cost sludge treatment
practices. Thus, it is imperative to mitigate toxic environmental contaminants for sustainable
development (Kümmerer et al., 2019).
A number of physical and chemical methods are currently being employed at large scale
for municipal wastewater management chiefly based on sewage treatment plants (STPs).
In addition to building expenses, upholding troubles in treatment plants has raised the query
of sustainability. Furthermore, surplus sewage sludge formed by these treatment plants
has posed more severe confines on release during the previous few decades (Vigueros and
Camperos, 2002). Several developing countries cannot meet the expense of construction of
STPs, necessitating the development of some eco-friendly and economically feasible machin-
ery for in situ wastewater management. Under such critical conditions, a few eco-friendly
techniques can resolve the limitations linked with secure and economically efficient
wastewater management machinery.
Bioremediation is an emerging and innovative technology because of its economic
feasibility, enhanced competence, and natural environment friendliness. The technology uses
various eco-friendly microbial processes to handle the ever-rising environmental pollution
problem. In such approaches, microbes adjust themselves against noxious wastes and environ-
mentally adapted microbial strains grow naturally, which subsequently convert a wide variety
of toxic chemicals into nontoxic forms. The microbial degradation of xenobiotics is based on
enzyme activities. It further includes rhizoremediation, phytoremediation (McCutcheon and
Jørgensen, 2008; Chang et al., 2009), and vermicomposting depending on the biological
activities involved. Phytoremediation is based on plant-assisted extenuation of pollutant
concentrations at the contaminated sites, whereas rhizoremediation includes the elimination
of specific pollutants from impure sites by the mutual interface of plant roots and appropriate
microbial flora (Rajkumar et al., 2012). Because bioremediation appears to be a promising
substitute to conventional cleanup machinery, extensive research is being carried out in this
field. Vermicomposting and vermifiltration are natural waste management procedures relying
on the utilization of worms to change organic wastes to form soil-enriching compounds
(Vettori et al., 2012). Domestic wastewater and industrial sludge management can be accom-
plished through these processes in a sustainable way (Benitez et al., 2002). In addition, a
substantial decrease in pathogens has been observed up to the end-products level. Therefore,
 2. Application of bioremediation for environmental pollutants cleanup 3
it can be securely used for land application. Biological methods have been reviewed and
acknowledged for remediation of environmental pollutant. In this chapter, we have tried to
focus on the application of biological methods which were used for effective waste treatment.
Several different strategies of bioremediation have also been discussed in later sections.

2. Application of bioremediation for environmental pollutants cleanup

In previous decades, rapid industrialization, urbanization, and indiscriminate resource

utilization by ever-increasing human population have increased the contamination of atmo-
sphere, land surfaces, and ground and surface waters. The wide-scale degradation of natural
resources constitutes a major threat to public health around the globe. Majority of contami-
nants affecting soil and water system are heavy metals, pesticides, petroleum hydrocarbons,
and large amount of toxic industrial effluents. These xenobiotics of anthropogenic origin are
recalcitrant in nature.
In the current scenario, restoration of degraded land, water, and soil system is only
possible by sustainable and eco-friendly processes. Among the various recent processes being
used for the abatement of environmental pollution, bioremediation is recognized as an
emerging methodology for the restoration of polluted environments. However, its ground
level applicability is restricted because of different climatic factors. Various microbes degrade
recalcitrant pollutants under aerobic or anaerobic conditions through complete mineraliza-
tion or cometabolism by using pollutants as their carbon sources. Bacteria and fungi have
been reported as favorable and potential candidates for both in situ and ex situ degradation
of organic pollutants present at contaminated sites. Furthermore, the microbes can be genet-
ically engineered for efficient degradation of environmental contaminants. Nevertheless,
extensive political and ethical concern restricts the wide-scale applicability of genetically
engineered organisms. The current biotechnological progress such as the use of proficient
microbial consortia, indigenous microbes, application of specific enzymes, biosurfactant,
and rhizoremediation are the new prospects in bioremediation technology. A schematic
representation of various methods and techniques applied for bioremediation of different
inorganic and organic contaminants has been illustrated in Fig. 1.1.

2.1 Bioremediation strategy for hydrocarbon contaminated water and soil

Bioremediation of hydrocarbon polluted soils and groundwater using bacteria has gained
immense consideration recently. Bacteria can degrade a large number of toxic hydrocarbons
under both aerobic and anaerobic circumstances. Benzene, toluene, ethyl benzene, and xylene
(BTEX) compounds are typical examples of hydrocarbons and are carcinogenic (de Graaff
et al., 2011) and neurotoxic in nature. Moreover, Environmental Protection Agency (EPA)
classified these hydrocarbons as priority pollutants requiring strict regulation. When organic
contaminants such as BTEX are released into the environment (Jin et al., 2013), the function
and structure of the microbial communities are generally affected. Although significant
researches on biodegradation of BTEX components by bacteria (Li et al., 2012) have been
reported, however, most of the studies have concentrated on the degradation of only one
or two components by bacterial isolate (Table 1.1). Furthermore, it is recognized that the
4 1. Bioremediation: a sustainable approach for management of environmental contaminants

(A) Bioremediation of
heavy metals

Biosurfactants Insitu Bio-

precipitation
Biosorption
Metal uptake by
organism Biological

Biorestoration
Enhanced
Cellulosic materials sulfate reduction
and agricultural wastes
Radionuclide
Immobilization
Insitu As removal by Fe
oxides & microorganisms

(B)
Bioremediation techniques

Natural attenuation Biopile

In-situ

Windrow

Ex-situ
Enhanced

Bioreactor

Land Farming

Bioslurping Bioventing Biosparging Phytoremediation

Xenobiotics
EDCs

Inorganic Organic
Pollutant Pollutant

Arsenic
Dye

FIGURE 1.1 Different strategies (A) and methods (B) of bioremediation of various inorganic and organic
contaminants.
 2. Application of bioremediation for environmental pollutants cleanup 5
TABLE 1.1 Microorganism involved in organic pollutant degradation.
Organic Degradation
pollutants Microbes condition Efficiency References

Polychlorinated Acinetobacter and Aerobic and e Wang et al. (2016b)

biphenyl Acidovorax anaerobic
Alkane and PAHs Alcanivorax, Marinobacter, e e Catania et al. (2015)
Thalassospira, Alteromonas,
and Oleibacter
Diesel degradation Pseudomonas sp., e e Zhang et al. (2014)
Bacillus subtilis

N-alkanes and PAHs Pseudomonas sp. WJ6 92.46% Xia et al. (2014)
Crude oil Colwellia, Cycloclasticus e e Wang et al. (2016a)
Phenolic compounds Microbial fuel cells Bio-electro- e Hedbavna et al. (2016)
chemical-systems
Crude oil Anabaena oryzae, Mixotrophic e Hamouda et al. (2016)
Chlorella kessleri, conditions
and its consortium
PAHs and Fusibacter, Alkaliphilus, Anaerobic e Folwell et al. (2016)
Naphthenic acids Desulfobacterium, Variovorax, biodegradation
Thauera, Hydrogenophaga
Pyrene Mycobacterium gilvum Immobilized on e Deng et al. (2016)
peanut shell
powder

biodegradation efficiency of one compound in a mixture can be influenced by additional

components. The side effect generated through the deprivation of one particular compound
can also influence the deprivation of another compound. Therefore, it is imperative to use an
integrated bioremediation approach by using the consortium of microbes for degradation of
petrochemicals containing hydrocarbons.

2.2 Bioremediation of heavy metal contaminated water

Bioremediation of heavy metal enriched soils and groundwater illustrates an immense
perspective for upcoming improvement because of its environmental compatibility and
probable expenditure efficiency (Baceva et al., 2014). It relies on microbial actions to
diminish, mobilize, or immobilize noxious heavy metals through biosorption,
biovolatilization, precipitation, surface complexation, and oxidationereduction processes
(Paul et al., 2014; Teixeira et al., 2014). Microorganism-directed oxidationereduction reactions
involving organic carbon, iron, manganese, and sulfur are the basic mechanisms influencing
heavy metals mobility. Under natural environmental conditions, there exists a complicated
interface among heavy metal pollutants and interacting microbes. These microorganisms
6 1. Bioremediation: a sustainable approach for management of environmental contaminants

have evolved specific resistance mechanism that permits their existence (Luo et al., 2014)
under heavy metal enriched conditions. These microbes are efficient to alleviate the concen-
tration of metal contaminants in their vicinity. Microorganisms are observed to proficiently
eliminate dissolved and suspended metals, particularly from a medium having very low
concentrations through bioaccumulation, surface complexation, and biosorption; therefore,
methods relying on microbial process offer a substitute to the conservative practices of metal
remediation (Dundar et al., 2014). Microbes reported for management of heavy metals are
tabulated in Table 1.2.

2.3 Bioremediation of dye contaminated water

Dyes are used for the permanent coloring of fibers and other consumer products
including foods, cosmetics, pharmaceuticals, papers, etc. The annual production of these
dyes is more than 7  107 tons, out of which 30,000e150,000 tons are discharged into
water (Anjaneya et al., 2011). In textile processing industries, a broad range of structurally
varied dyes are utilized, and therefore, effluents from these industries are tremendously
erratic in composition. In general, wastewater generated from dyeing industries contains
up to 50% dye of the originally used concentration, together with several other chemical
components, dispersing agents, fixatives, heavy metals, and inorganic salts. Generally,
dyes are visibly detectable at very low quantity (1 mg L 1), which may cause water
pollution and changes to normal functioning of aquatic ecosystem by reducing dissolved
oxygen contents, due to reduced photosynthetic activity of submerged plants caused by
very weak penetration of light into water imposed by dyes. Hence, the toxicity exerted
by textile effluents due to synergistic actions of physical appearance and chemical constit-
uents is raising an environmental concern for their minimization to permissible limits. It is
identified that 90% of reactive dyes get their way into treatment plants that may remain
unaffected and released as such into rivers (Abadulla et al., 2000). Several dyes presently
being utilized are not susceptible to degradation or elimination with physicochemical
methods. Most importantly, often the degradation by-products of physicochemical methods
are even more noxious than the parent dye used. Color can be eliminated from wastewater
by chemical and physical processes including adsorption, precipitation, flocculation, and
oxidation followed by filtration and electrochemical methods. These techniques are
relatively expensive and have operational troubles (Kapdan et al., 2000). Numerous
troubles, particularly the high dose requirement of chemicals and extensive power
consumption, limit their realistic purpose. Consequently, the biodegradation of synthetic
dyes has gained rising magnetism because of its natural ecological resemblance, lesser
treatment costs, and elevated efficiency.
Currently, several scientific groups across the world are involved in manipulating the
bacterial genetic constitution to improve their dye degradation ability to accelerate the
bioremediation process. Different microbial consortium can degrade numerous azo-dyes aero-
bically and anaerobically. Actually, bacterial consortia are supposed to be more beneficial for
complete dye degradation. In mixed culture, the toxic intermediates generated because of the
activity of one bacterium are degraded by other bacteria of consortium (Forgacs et al., 2004;
Jain et al., 2012). Thus, the degradation of dye will depend on origin and chemical nature of
dyes and microorganism used in the consortium.
 2. Application of bioremediation for environmental pollutants cleanup 7
TABLE 1.2 List of biological agents responsible for the remediation of heavy metals.
Heavy
metals Biological agent Processes Efficiency References

Hexavalent Geotrichum sp. Bioleaching system 94.8% Qu et al. (2018)

chromium and Bacillus sp.
Arsenic Shewanella sp. Transport of e Lim et al. (2007)
arsenic, coupled with
microbe-mediated
biogeochemical processes.
As(V) was reduced to
As(III)
Arsenic Eichhornia crassipes Bioaccumulation e Alvarado et al. (2008)
and Lemna minor
Arsenic Shewanella Microbial leaching e Weisener et al. (2011)
putrefaciens
200R and Shewanella
sp. ANA
Mercury Functional Enzyme degradation e Dash and Das (2012)
genes are
merA and merB
Mercury Bacillus cereus Bioaccumulating e Sinha et al. (2012)
Arsenic Pseudomonas, e e Das et al. (2014)
Acinetobacter,
Klebsiella,
and Comamonas
Mercury Filamentous fungi Biosorption 97.50% and 98.73% Kurniati et al. (2014)
Arsenic Brevibacillus sp. e e Mallick et al. (2014)
KUMAs2
Inorganic Bacillus cereus Volatilization 96.4% Dash and Das (2015)
mercury BW-03(pPW-05) and biosorption
Arsenic Bacillus sp. and e 51.45%e51.99% for Dey et al. (2016)
Aneurinibacillus As(III) and 50.37%
aneurinilyticus e53.29% for As(V)
Lead Rhodobacter sphaeroides e e Li et al. (2016)
Arsenic Bacillus aryabhattai e e Singh et al. (2016)
(NBRI014)
Hexavalent Sporosarcina Bioreduction e Zhao et al. (2016)
chromium saromensis M52
Arsenic Pseudomonas e e Akhter et al. (2017)
stutzeri TS44
Chromium Aspergillus tamarii In batch and e Ghosh et al. (2017)
complex continuous bioreactors
Lead Pararhodobacter sp. Calcium carbonate e Mwandira et al. (2017)
precipitation technique
8 1. Bioremediation: a sustainable approach for management of environmental contaminants

2.3.1 Bioremediation approaches used for dye degradation

Dye decolorization is started by anaerobic reduction reaction performed by azo-reductases
or azo-bonds breakage under aerobic or anaerobic condition leading to the formation of
aromatic amines because of physiological and biochemical activities of the mixed bacterial
community (Sponza and Isik, 2004). A list of microorganisms involved in dye degradation
is presented in Table 1.3.
A detailed description on various processes for dye degradation has been presented below:

2.3.1.1 Aerobic treatment

Reports on bacterial degradation of azo-dyes are very limited; however, some microorgan-
isms have shown their capacity of dye reduction. Pseudomonas aeruginosa has been
demonstrated to degrade commercially exploited textile and tannery dye Navitan Fast
Blue SSR in a medium amended with glucose as a carbon source under aerobic condition
(Garg and Thripathi, 2017). Kalyani et al. (2009) have also observed that some bacterial strains
have capability to degrade dye under the aerobic environments.

TABLE 1.3 List of potential organisms responsible for degradation of dyes.

Experimental
Dye Organism condition Efficiency Reference

Direct Red-31 dye Chlorella pyrenoidosa Batch experiments/ 96% Decolorization Sinha et al. (2016)
strain NCIM 2738 continuous cyclic with 40 mg L 1
bioreactor treatment dye at pH 3
Reactive green Fungal strain e 97.9% Decolorization Sinha and Osborne
dye (RGD) VITAF-1 of RGD within (2016)
48 h at 30  2 C
Crystal violet Trichoderma asperellum e Shanmugam et al.
(2017)
Industrial Chaetomium globosum Stirred and static Dye removal Manai et al. (2016)
textile effluent IMA1 KJ472923 batch cultures adsorption (8%) and
degradation (92%)
Hair dye Enterobacter cloacae e e Maiti et al. (2017)
DDB I
Azure B dye Bacillus sp. MZS10 93.55% (0.04 g L 1) Li et al. (2014)
within 14 h
Resonance Bacterial e e Kumar et al. (2012)
stabilized and consortium-AVS,
heteropolyaromatic consisting of Pseudomonas
dyes desmolyticum NCIM 2112,
Kocuria rosea MTCC 1532,
and Micrococcus glutamicus
NCIM 2168
 2. Application of bioremediation for environmental pollutants cleanup 9
2.3.1.2 Anaerobic treatment
Under anaerobic condition, azo-dye reduction is achieved by breakage of the azo-bonds.
Under the anaerobic situation, cleaving of dyes occurs, which produces toxic aromatic amines
by bacterial metabolism (Bhatt et al., 2005).

2.3.1.3 Anoxic treatment

Anoxic degradation of different dyes by facultative anaerobic and mixed aerobic
microorganisms is reported in different studies (Kapdan and Alparslan, 2005). Although
several microorganisms are capable of growing under aerobic condition, however, the dye
is degraded only under anoxic environments. Several pure bacterial cultures including those
of Pseudomonas luteola, Aeromonas hydrophila, Bacillus subtilis, and Proteus mirabilis are known
to anoxically degrade azo-dyes (Sandhya et al., 2005).
2.3.1.4 Sequential degradation of dyes
It has been suggested that aromatic amines produced after anaerobic degradation of
azo-dyes can be despoiled subsequently under aerobic environment. The applicability of
this approach was firstly proven for Mordant Yellow, a sulfonated azo-dye. After aeration,
complete mineralization of amine by microbial activities is observed.

2.4 Vermi-biofiltration of wastewater

Vermi-biofiltration is a natural waste management method relying on worms to alter
organic wastes to form soil enriching compounds (Romero et al., 2006). Domestic wastewater
and industrial sludge management can be lodged through these methods in a
sustainable way (Solis-Mejia et al., 2012). A substantial decrease in pathogens has been
observed in the final product to a level that can be securely useful to land (Najar and
Khan, 2013). The practice can be used at small scale for organic waste handling or municipal
waste management (Karmakar et al., 2012). Vermi-biofiltration is a method that acclimatizes
conventional vermicomposting method into an inert wastewater handling procedure by
means of epigeic earthworms (Garg et al., 2009; Gupta and Garg, 2009). According to
Komarowski (2001), vermi-biofiltration scheme uses suspended solids that are placed on
an upper portion of a filter and developed by earthworms and feed to soil microorganisms
harnessed in vermifilter. The solubilized and non-soluble organic and inorganic
suspensions are removed by adsorption and stabilization process through multifaceted
degradation reactions that occurs in soil occupied by aerobic microorganisms and
earthworm. In general, acclimatized vermibed earthworms collect numerous organic
contaminants in the vicinity of surrounding soil system (Sangwan et al., 2008) through
passive absorption by body wall and also by intestinal uptake during the course of soil
passage via gut (Mahmood et al., 2013).

2.5 Bioremediation of pesticide contamination

The annual global utilization of pesticides is approximately 2 million tonnes, of which 24%
is used by the United States, 45% in Europe, and rest 25% by remaining parts of the world.
India is reported to consume about 3.8% of the total pesticide produced worldwide.
10 1. Bioremediation: a sustainable approach for management of environmental contaminants

The pesticide consumption for agricultural applications is 0.5, 6.6, and 12.0 kg ha 1 for India,
Korea, and Japan, respectively (Gupta, 2004). Earlier, the pesticide application, as anticipated,
was quite helpful in reducing crop yield loss happening because of insect pest attack and thus
opened the way for enhancement in crop productivity. However, extensive application of
chemically synthesized pesticides has given rise to contamination of the natural environment
and also caused several chronic impacts on human society (Bhanti and Taneja, 2007).
The stable nature, long-term existence in the natural environment, biological magnification,
and accumulation at various trophic levels due to their lack of selectivity, and organochlo-
rines have been reported to be responsible for pest resistance development and hazardous
effect on nontarget organisms (Carson, 1962). The possible threats to all living organisms
arising from the indiscriminate application of these agricultural chemicals have now
emerged as one of the most potent environmental or health problems particularly in Third
World countries. Pesticides are mainly criticized for their availability in drinking water,
vegetables, mammalian blood, human food, milk products, fat samples, and other food
commodities. There is no contradiction regarding the human health hazards associated
with the application and chronic exposure to pesticides. Hence, the presence of pesticide
residue in different environmental samples via contaminated food chain is a direct indication
of acute or chronic exposure and average body risk to persistent pesticides.

2.6 Removal of pharmaceutical and personal care products by biological

degradation processes
Microorganisms are known to degrade the environmental pollutants by using the contam-
inants for their vital physiological and biochemical processes, and under certain conditions,
different microbes can coordinate each other to degrade the pollutants. The following
subsections represent the role of pure and mixed culture in biodegradation of pharmaceutical
and personal care products (PPCPs).

2.6.1 Pure cultures

Several experimental investigations have demonstrated that pure cultures of numerous
algae, bacteria, and fungi obtained from different samples including activated sludge,
wastewater, or sediment can be utilized to treat the commonly detected pollutants such as
iopromide (Liu et al., 2013), carbamazepine (Popa et al., 2014), ibuprofen (Almeida et al.,
2013), sulfamethoxazole (Jiang et al., 2012), diclofenac (Hata et al., 2010), paracetamol
(Dang et al., 2013), and triclosan (Zhao et al., 2013). The pure cultures of different organisms
efficient in degradation of various PPCPs have been presented in Table 1.4. A few pure
cultures obtained from activated sludge showed efficiency in removal of a number of PPCPs.
For example, Achromobacter denitrificans is able to mineralize sulfamethoxazole and other
sulfonamides (Reis et al., 2018). Apart from this, several pure cultures can consume special-
ized PPCPs as sole source of C and energy, though with changed degradation pathways
(Dang et al., 2013; Almeida et al., 2013). For example, Delftia tsuruhatensis, P. aeruginosa,
and Stenotrophomonas can mineralize paracetamol. The study concluded that D. tsuruhatensis
and P. aeruginosa contributed very less in paracetamol removal, while biosorption by Steno-
trophomonas contributed significantly in removal of paracetamol. The differences could be due
to involvement of different enzymes participating in degradation. Sometimes pure cultures
 2. Application of bioremediation for environmental pollutants cleanup 11
TABLE 1.4 List of microbes responsible for degradation of pharmaceuticals and pesticides.
Pharmaceuticals/ Degradation Degradation
pesticides Microbes condition efficiency Reference

Atrazine Citricoccus Alkaline environment e Yang et al. (2018)

Tebuconazole Serratia marcescens e 70.42%, 96.46% Wang et al. (2018b)
strain B1 in 30 days
Lincomycin Clostridium sp. strain 62.03% Wang et al. (2018a)
LCM-B
Chlorimuron-ethyl Enterobacter ludwigii e 83.1%e83.9% Pan et al. (2018b)
sp. CE-1
Ciprofloxacin Thermus sp. e e Pan et al. (2018a)
Levofloxacin Chlorella vulgaris e e Xiong et al. (2017)
Triclosan Geitlerinema sp. and e 82.10%e92.83% Tastan et al. (2017)
Chlorella sp. (3.99 mg L 1) of
triclosan in
10 days
Organochlorine Streptomyces e 99.8% Fuentes et al. (2017)
pesticide (OCP) consortium

Pharmaceutically White-rot fungi Enzymes e Naghdi et al. (2018)

active compounds immobilization,
fungal reactors
Mixture of pesticides Streptomyces e e Fuentes et al. (2017)
consortium
Atrazine and 2,4- Pseudomonas Aerobic e Carboneras et al. (2017)
dichlorophenoxyacetic and Rhodococcus biodegradation
acid
Acenaphthene and Pseudomonas e 98.8% and 98.6% Barman et al. (2017)
naphthalene mendocina
Pesticides Actinobacteria e e Alvarez et al. (2017)
Triazolopyrimidine Aspergillus e e Sondhia et al. (2016)
sulfonamide
OCP Native bacteria e e Kopytko (2016)
Atenolol, gemfibrozil, e Activated sludge e Arya et al. (2016)
and ciprofloxacin process, submerged
attached biofilter,
and membrane
bioreactor
Penicillin G Klebsiella pneumoniae e e Wang et al. (2015)
Z1
Pharmaceuticals Ammonia-oxidizing e 80% Peng et al. (2015)
bacteria

(Continued)
12 1. Bioremediation: a sustainable approach for management of environmental contaminants

TABLE 1.4 List of microbes responsible for degradation of pharmaceuticals and pesticides.dcont'd
Pharmaceuticals/ Degradation Degradation
pesticides Microbes condition efficiency Reference

Triclosan Aspergillus e e Ertit Tastan and

versicolor Dönmez (2015)
Organophosphorus Stenotrophomonas sp. e e Deng et al. (2015)
pesticides G1
Caffeine, e Growth e Vasiliadou et al. (2013)
sulfamethoxazole, reactor
ranitidine,
carbamazepine,
and ibuprofen
Endosulfan Alcaligenes e 87.5% Kong et al. (2013)
faecalis JBW4 (a-endosulfan)
and 83.9%
(b-endosulfan)
in 5 days
Organophosphorus Serratia marcescens e e Cyco

n et al. (2013)
pesticides
Pharmaceutically Active biomass in e e Majewsky et al. (2011)
active compounds activated sludge
Endosulfan Aspergillus niger e e Bhalerao and Puranik
(2007)

are unable to utilize few PPCPs as carbon and energy source because of their substrate
specificity. Under such conditions, other substrate needs to be amended in medium to fulfill
the requirement of carbon and energy source so as to maintain the vital metabolic activities at
optimal rate. For instance, the stable nature of carbamazepine often does not allow the
efficient degradation by microbes. But, mixed consortium consisting of an unidentified basid-
iomycete member (Santoso et al., 2011) and Streptomyces MIUG (Popa et al., 2014) was noticed
to breakdown the carbamazepine in medium supplemented with glucose. Along with
carbamazepine, iopromide was also susceptible to degradation after additional substrates
were amended in the medium. Liu et al. (2013) demonstrated that Pseudomonas sp. I-24 bears
the ability to degrade iopromide with starch as primary supplement. Diclofenac has been
reported to display high resistance to biological degeneration in activated sludge system.
However, Hata et al. (2010) showed that white-rot fungi is capable to fully remove diclofenac
to the safety limits prescribed for the organisms without any added supplement. The micro-
bial enzyme activation has been suggested as another important factor leading to PPCPs
degradation. The biological breakdown of PPCPs relies on whether microbes are able to
synthesize the essential enzymes responsible for degradation. For example, triclosan is
known to stimulate Nitrosomonas europaea to synthesize ammonia monooxygenase to facilitate
fast degradation of triclosan (Roh et al., 2009). However, few PPCPs including ciprofloxacin,
tetracycline, and trimethoprim do not readily stimulate microbes to synthesize the specific
enzyme, thus, leading to inefficient biodegradation. Most importantly, there is no report
 2. Application of bioremediation for environmental pollutants cleanup 13
on contribution of any pure culture isolated so far in decomposition of ciprofloxacin, tetracy-
cline, and trimethoprim. Therefore, to facilitate the effective biodegradation of hazardous
recalcitrant PPCPs, the primary requirement is to stimulate the microorganisms with the
ability to produce the specific degradative enzyme in a given environmental condition.

2.6.2 Mixed cultures

Mixed cultures are more efficient in biological degradation of the PPCPs as compared to
pure cultures because under some environmental conditions it is very hard to isolate the
pure culture. Limited study has been performed to analyze the efficiency of mixed culture
for PPCPs removal (Khunjar et al., 2011). Mixed culture has the efficiency to remove PPCPs.
Khunjar et al. (2011) described the role played by mixed culture of heterotrophic and
ammonia-oxidizing bacteria for enhanced elimination of 17a-ethinylestradiol. Actually, the
commonly employed biological treatment methods rely on synergistic actions of mixed
cultures to eliminate PPCPs. However, sometimes activated sludge demonstrates low PPCPs
elimination rate. Therefore, experiments have been carried out to enhance the
PPCPs degradation through activated sludge process. High rate removal of PPCPs
through metabolic activities of mixed culture present in activated sludge has been described
by Zhao et al. (2013). Interestingly, mixed culture has been reported to facilitate very fast
decomposition of mixed PPCPs as compared to degradation of a single PPCP
(Vasiliadou et al., 2013). This can be explained by the fact that few members of mixed PPCPs
can serve as C and energy source for mixed culture, thus facilitating further degradation of
other PPCPs. Hence, mixed cultures have been proposed as a potential alternative for
accelerated degradation of PPCPs.

2.6.3 Activated sludge process

Activated sludge technique has been largely employed for biological treatment in
traditionally used wastewater treatment plants. The PPCPs degradation in biological
treatment has been attributed to the combinatorial action of volatilization, surface binding,
and microbial decomposition. However, the role of volatilization and adsorption processes
in degradation of PPCPs is minimal (Li et al., 2015). Generally, volatilization happens simul-
taneously with aeration. The adsorption of PPCPs during biological treatment is significantly
affected by physicochemical attributes of compounds to be degraded. Furthermore, changes
in environmental variables including pH, oxygen content, temperature, the composition of
the microbial community, and nutrient status can also largely influence the overall efficiency
of activated sludge system applied for PPCPs elimination. Biodegradation is suggested as
the major phenomenon responsible for PPCPs elimination in activated sludge process.
Therefore, to improve the degradation of PPCPs, an effective strategy must be adapted to
increase the decomposition. Nevertheless, microbial decomposition is not always efficient
in the elimination of environmental contaminants due to the low abundance of microbes
responsible for degradation. These impediments can be resolved by prior acclimatization
to contaminants, bioaugmentation (Wang et al., 2004) and biostimulation. Through adapta-
tion and bioaugmentation, the abundance of the pure or mixed culture of microorganisms
effective in contaminant degradation can be improved in biological treatment methodologies.
Plosz et al. (2012) have designed a model for xenobiotic trace chemicals and utilized it to
forecast and monitor the environmental factors affecting the elimination of carbamazepine
and diclofenac in activated sludge system.
Another random document with
no related content on Scribd:
capable of producing so much sound. I have never observed this
habit upon a dull or cloudy day.”
Mr Nuttall having presented me with the nest of this species
attached to the twig to which the bird had fastened it, my amiable
friend Miss Martin has figured it for me, as well as the plant, about
which these lovely creatures are represented. The nest, which
measures two inches and a quarter in height, and an inch and three
quarters in breadth, at the upper part, is composed externally of
mosses, lichens, and a few feathers, with slender fibrous roots
interwoven, and lined with fine cottony seed-down.

Trochilus rufus, Gmel. Syst. Nat. vol. i. p. 497.

Trochilus collaris, Lath. Ind. Ornith. vol. i. p. 318.
Trochilus (Selasphorus) Rufus, Swainson.
Cinnamon or Nootka Humming Bird, Richards. and Swains. Fauna Bor.-
Amer. vol. ii. p. 324.

Adult Male. Plate CCCLXXIX. Figs. 1, 2.

Bill long, straight, subulate, somewhat depressed at the base, acute;
upper mandible with the dorsal line straight, the ridge narrow at the
base, broad and convex toward the end, the sides convex, the edges
overlapping, the tip acuminate; lower mandible with the angle very
long and extremely narrow, the dorsal line straight, the edges erect,
the tip acuminate. Nostrils basal, linear.
Head of ordinary size, oblong; neck short; body slender. Feet very
small; tarsus very short, feathered more than half-way down, toes
small; the lateral equal, the middle toe not much longer, the hind toe
a little shorter than the lateral, anterior toes united at the base; claws
rather long, arched, compressed, laterally grooved, very acute.
Plumage soft and blended; feathers on the throat, fore part and sides
of the neck oblong-obovate, with the filaments towards the end
thickened and flattened, with metallic gloss, those on the sides of the
neck elongated and erectile. Wings rather short, extremely narrow,
falcate, pointed; the primaries rapidly graduated, the second being
longest, but only slightly longer than the first; these two quills taper to
a point; the rest are broader, and gradually become less pointed; the
secondaries are extremely short, and only five in number. Tail rather
long, broad, graduated, the lateral feathers four and a half twelfths of
an inch shorter than the central; the latter are extremely broad,
measuring four and a half twelfths across, and the rest gradually
diminish to the lateral, which are very narrow; all obtusely pointed.
Bill brownish-black; toes brown, claws dusky. The general colour of
the upper parts is bright cinnamon or reddish-orange; the head
bronzed green, the wings dusky, the coverts glossed with green, the
primaries with purplish; each of the tail-feathers has a narrow
longitudinal lanceolate median streak toward the end. The loral
space, a narrow band over the eye, another beneath it, and the
auriculars are reddish-orange; the scale-like feathers of the throat
and sides of the neck are splendent fire-red, purplish-red, yellowish-
red, greenish-yellow or yellowish-green, according to the light in
which they are viewed; behind them, on the lower part of the neck, is
a broad band of reddish-white; the rest of the lower parts are like the
upper, the abdomen inclining to white.
1/2
Length to end of tail 3 7/12 inches; bill along the ridge 7 /12, along
the edge of lower mandible 9 1/4/12; wing from flexure 1 7 1/4/12; tail
1 3 1/2/12; tarsus 1 1/2/12; hind toe 1 1/2/12, its claw 1 1/4/12; middle toe
2 1/4/ , its claw 1
1/2
/12.
12

Adult Female. Plate CCCLXXIX. Fig. 3.

The Female has the bill and feet coloured as in the male. The upper
parts are gold-green, the head inclining to brown; the wings as in the
male; the tail-feathers reddish-orange at the base, brownish-black
toward the end, the tip white. The lower parts are white, tinged with
rufous, of which colour, especially, are the sides; the throat marked
with roundish spots of metallic greenish-red.

Length to end of tail 3 7 1/2/12 inches; bill along the ridge 8 3/4/12; wing
from flexure 1 10/12; tail 1 1 1/2/12.

The above descriptions are from two individuals shot by Dr

Townsend on the “Columbia River, 30th May 1835.” A “young male,
Columbia River, 29th May 1835,” resembles the female as above
described, differing only in having the metallic spots on the throat
larger. A “young female, Columbia River, June 10th 1835,” differs
from the adult only in wanting the metallic spots on the throat, which
is spotted with greenish-brown.

Cleome heptaphylla.

The beautiful plant represented in the plate belongs to Tetradynamia

Siliquosa of the Linnæan arrangement, and to the genus Cleome,
characterized by having three nectariferous glandules at each corner
of the calyx, the lower excepted; all the petals ascending; the
germen stipitate; the siliqua unilocular, two-valved. The species, C.
heptaphylla, is distinguished by its septenate leaves, of which the
leaflets are lanceolate, acuminate, and of a deep green colour. It
grows in South Carolina and Georgia.
 TENGMALM’S OWL.

Strix Tengmalmi, Gmel.

PLATE CCCLXXX. Male and Female.

I procured a fine male of this species at Bangor, in Maine, on the

Penobscot River, in the beginning of September 1832; but am
unacquainted with its habits, never having seen another individual
alive. Dr Townsend informs me that he found it first on the Malade
River Mountains, where it was so tame and unsuspicious, that Mr
Nuttall was enabled to approach within a few feet of it, as it sat
upon the bushes. Dr Richardson gives the following notice
respecting it in the Fauna Boreali-Americana:—“When it accidentally
wanders abroad in the day, it is so much dazzled by the light of the
sun as to become stupid, and it may then be easily caught by the
hand. Its cry in the night is a single melancholy note, repeated at
intervals of a minute or two. Mr Hutchins informs us that it builds a
nest of grass half-way up a pine tree, and lays two white eggs in the
month of May. It feeds on mice and beetles. I cannot state the extent
of its range, but believe that it inhabits all the woody country from
Great Slave Lake to the United States. On the banks of the
Saskatchewan it is so common that its voice is heard almost every
night by the traveller, wherever he selects his bivouac.”

Strix Tengmalmi, Gmel. Syst. Nat. vol. i. p. 291.—Lath. Ind. Ornith. vol. i. p.
65.
 Strix Tengmalmi, Tengmalm’s Owl, Swains. and Richards. Fauna Bor.-
Amer. vol. ii. p. 94.

Adult Male. Plate CCCLXXX. Fig. 1.

Bill short, very deep, strong; upper mandible with its dorsal line
curved from the base, its ridge convex, as are the sides, the edges
sharp and incurved anteriorly, the tip very acute, and at its extremity
nearly perpendicular; the cere short, and bare on its upper part; the
lower mandible has the angle broad and short, the dorsal line slightly
convex, the edges inflected, towards the end incurved, with a notch
on each side close to the abruptly-rounded tip. Nostrils broadly
elliptical, oblique, in the fore part of the cere, which bulges
considerably behind them.
The head is extremely large, roundish, when viewed from above
somewhat triangular; the eyes large. The conch of the ear very large,
of an elliptical form, extending from the base of the lower jaw to near
the top of the head, being an inch and a quarter in length, with an
anterior semicircular operculum stretching along its whole length,
and an elevated margin behind. The neck is very short and thin; the
body very slender; but both appear very full on account of the vast
mass of plumage. The feet are rather short, and strong; the tarsi and
toes covered with very soft downy feathers, the extremities of the
latter with two scutella. The claws are slender, tapering to a fine
point, compressed, and curved.
The facial disk is complete, as is the ruff. The plumage is full, very
soft, and blended; the feathers broadly oblong and rounded. The
wings are rather long, very broad, much rounded; the third primary
longest, the fourth almost equal, the second four-twelfths of an inch
shorter, the first equal to the seventh; the barbs of the outer web of
the first, of half the second, and the terminal part of the third, free
and recurved. Tail of moderate length, arched, slightly rounded, of
twelve broad, rounded feathers.
Bill greyish-brown, yellowish-white at the end; claws yellowish-
brown, their tips dusky. The general colour of the upper parts is
greyish-brown tinged with olive. The feathers of the head have an
elliptical central white spot; those of the neck are similarly marked
with larger white spots, of which some are disposed so as to form a
semicircular band; the scapulars have two or four large round spots
near the end, and some of the dorsal feathers and wing-coverts have
single spots on the outer web. All the quills have marginal white
spots on both webs, arranged in transverse series, there being six
on the outer web of the third quill. On the tail are five series of
transversely elongated narrow white spots. The disk is yellowish-
white, anteriorly black; the ruff yellowish-white, mottled with dusky.
The throat is brown, the chin white. The general colour of the lower
parts is yellowish-white, longitudinally streaked with brown, some of
the feathers of the sides have two white spots near the end; the
tarsal and digital feathers greyish-yellow, with faint transverse bars of
brown.
Length to end of tail 11 inches; wing from flexure 6 10/12; bill along
the ridge 1; tarsus 11/12; hind toe 5/12, its claw 5/12; middle toe 9/12, its
claw 8/12.

Adult Female. Plate CCCLXXX. Fig. 2.

The Female resembles the male, but is considerably larger.
 SNOW GOOSE.

Anser hyperboreus, Bonap.

PLATE CCCLXXXI. Adult Male and Young Female.

The geographical range of the Snow Goose is very extensive. It has

been observed in numerous flocks, travelling northward, by the
members of the recent overland expeditions. On the other hand, I
have found it in the Texas, and it is very abundant on the Columbia
River, together with Hutchins’s Goose. In the latter part of autumn,
and during winter, I have met with it in every part of the United States
that I have visited.
While residing at Henderson on the Ohio, I never failed to watch the
arrival of this and other species in the ponds of the neighbourhood,
and generally found the young Snow Geese to make their
appearance in the beginning of October, and the adult or white birds
about a fortnight later. In like manner, when migrating northward,
although the young and the adult birds set out at the same time, they
travel in separate flocks, and, according to Captain Sir George
Back, continue to do so even when proceeding to the higher
northern latitudes of our continent. It is not less curious that, during
the whole of the winter, these Geese remain equally divided, even if
found in the same localities; and although young and old are often
seen to repose on the same sand-bar, the flocks keep at as great a
distance as possible.
The Snow Goose in the grey state of its plumage is very abundant in
winter, about the mouths of the Mississippi, as well as on all the
muddy and grassy shores of the bays and inlets of the Gulf of
Mexico, as far as the Texas, and probably still farther to the south-
west. During the rainy season, it betakes itself to the large prairies of
Attacapas and Oppellousas, and there young and adult procure their
food together, along with several species of Ducks, Herons, and
Cranes, feeding, like the latter, on the roots of plants, and nibbling
the grasses sideways, in the manner of the Common Tame Goose.
In Louisiana I have not unfrequently seen the adult birds feeding in
wheat fields, when they pluck up the plants entire.
When the young Snow Geese first arrive in Kentucky, about
Henderson for instance, they are unsuspicious, and therefore easily
procured. In a half-dry half-wet pond, running across a large tract of
land, on the other side of the river, in the State of Indiana, and which
was once my property, I was in the habit of shooting six or seven of
a-day. This, however, rendered the rest so wild, that the cunning of
any “Red Skin” might have been exercised without success upon
them; and I was sorry to find that they had the power of
communicating their sense of danger to the other flocks which
arrived. On varying my operations however, and persevering for
some time, I found that even the wildest of them now and then
suffered; for having taken it into my head to catch them in large
traps, I tried this method, and several were procured before the rest
had learned to seize the tempting bait in a judicious manner.
The Snow Goose affords good eating when young and fat; but the
old Ganders are tough and stringy. Those that are procured along
the sea-shores, as they feed on shell-fish, fry and marine plants,
have a rank taste, which, however suited to the palate of the epicure,
I never could relish.
The flight of this species is strong and steady, and its migrations over
the United States are performed at a considerable elevation, by
regular flappings of the wings, and a disposition into lines similar to
that of other Geese. It walks well, and with rather elevated steps; but
on land its appearance is not so graceful as that of our common
Canada Goose. Whilst with us they are much more silent than any
other of our species, rarely emitting any cries unless when pursued
on being wounded. They swim buoyantly, and, when pressed, with
speed. When attacked by the White-headed Eagle, or any other
rapacious bird, they dive well for a short space. At the least
appearance of danger, when they are on land, they at once come
close together, shake their heads and necks, move off in a contrary
direction, very soon take to wing, and fly to a considerable distance,
but often return after a time.
I am unable to inform you at what age the Snow Goose attains its
pure white plumage, as I have found that a judgment formed from
individuals kept in confinement is not to be depended upon. In one
instance at least, a friend of mine who had kept a bird of this species
four years, wrote to me that he was despairing of ever seeing it
become pure white. Two years after, he sent me much the same
message; but, at the commencement of next spring, the Goose was
a Snow Goose, and the change had taken place in less than a
month.
Dr Richardson informs us that, this species “breeds in the barren
grounds of Arctic America, in great numbers. The eggs of a
yellowish-white colour, and regularly ovate form, are a little larger
than those of the Eider Duck, their length being three inches, and
their greatest breadth two. The young fly in August, and by the
middle of September all have departed to the southward. The Snow
Goose feeds on rushes, insects, and in autumn on berries,
particularly those of the Empetrum nigrum. When well fed it is a very
excellent bird, far superior to the Canada Goose in juiciness and
flavour. It is said that the young do not attain the full plumage before
their fourth year, and until that period they appear to keep in
separate flocks. They are numerous at Albany Fort in the southern
part of Hudson’s Bay, where the old birds are rarely seen; and, on
the other hand, the old birds in their migrations visit York Factory in
great abundance, but are seldom accompanied by the young. The
Snow Geese make their appearance in spring a few days later than
the Canada Geese, and pass in large flocks both through the interior
and on the coast.”
The young birds of this species begin to acquire their whiteness
about the head and neck after the first year, but the upper parts
remain of a dark bluish colour until the bird suddenly becomes white
all over; at least, this is the case with such as are kept in captivity.
Although it is allied to the White-fronted or Laughing Goose, Anser
albifrons, I was surprised to find that Wilson had confounded the
two species together, and been of opinion that the Bean Goose also
was the same bird in an imperfect state of plumage. That excellent
ornithologist tells us that “this species, called on the sea-coast, the
Red Goose, arrives in the river Delaware, from the north, early in
November, sometimes in considerable flocks, and is extremely noisy,
their notes being shriller and more squeaking than those of the
Canada, or common Wild Goose. On their first arrival, they make but
a short stay, proceeding, as the depth of winter approaches, farther
south; but from the middle of February, until the breaking up of the
ice in March, they are frequently numerous along both shores of the
Delaware, about and below Reedy Island, particularly near Old Duck
Creek, in the State of Delaware. They feed on roots of the reeds
there, which they tear up like hogs.”
This species is rare both in Massachusetts and South Carolina,
although it passes over both these States in considerable numbers,
and in the latter some have been known to alight among the
common domestic Geese, and to have remained several days with
them. My friend Dr Bachman, of Charleston, South Carolina, kept a
male Snow Goose several years along with his tame Geese. He had
received it from a friend while it was in its grey plumage, and the
following spring it became white. It had been procured in the autumn,
and proved to be a male. In a few days it became very gentle, and
for several years it mated with a common Goose; but the eggs
produced by the latter never hatched. The Snow Goose was in the
habit of daily frequenting a mill-pond in the vicinity, and returning
regularly at night along with the rest; but in the beginning of each
spring it occasioned much trouble. It then continually raised its head
and wings, and attempted to fly off; but finding this impossible, it
seemed anxious to perform its long journey on foot, and it was
several times overtaken and brought back, after it had proceeded
more than a mile, having crossed fences and plantations in a direct
course northward. This propensity cost it its life: it had proceeded as
far as the banks of the Cooper River, when it was shot by a person
who supposed it to be a wild bird.
In the latter part of the autumn of 1832, whilst I was walking with my
wife, in the neighbourhood of Boston in Massachusetts, I observed
on the road a young Snow Goose in a beautiful state of plumage,
and after making some inquiries, found its owner, who was a
gardener. He would not part with it for any price offered. Some
weeks after, a friend called one morning, and told me that this
gardener had sent his Snow Goose to town, and that it would be sold
by auction that day. I desired my friend to attend the sale, which he
did; and before a few hours had elapsed, the bird was in my
possession, having been obtained for 75 cents! We kept this Goose
several months in a small yard at the house where we boarded,
along with the young of the Sand-hill Crane, Grus Americana. It was
fed on leaves and thin stalks of cabbage, bread, and other vegetable
substances. When the spring approached, it exhibited great
restlessness, seeming anxious to remove northward, as was the
case with Dr Bachman’s bird. Although the gardener had kept it four
years, it was not white, but had the lower part of the neck and the
greater portion of the back, of a dark bluish tint, as represented in
the plate. It died before we left Boston, to the great regret of my
family, as I had anticipated the pleasure of presenting it alive to my
honoured and noble friend the Earl of Derby.
There can be little doubt that this species breeds in its grey plumage,
when it is generally known by the name of Blue-winged Goose, as is
the case with the young of Grus Americana, formerly considered as
a distinct species, and named Grus Canadensis.

Anas hyperborea, Gmel. Syst. Nat. vol. i. p. 504.—Lath. Ind. Orn. vol. ii. p.
837.
Snow Goose, Anas hyperborea, Wils. Amer. Ornith. vol. viii. p. 76, pl. 68,
fig. 3, Male, and p. 89, pl. 69, fig. 5, Young.
Anser hyperboreus, Ch. Bonaparte, Synopsis of Birds of United States, p.
376.
Anser hyperboreus, Snow Goose, Richards. and Swains. Fauna Bor.-
Amer. vol. ii. p. 467.
Snow Goose, Nuttall, Manual, vol. ii. p. 344.

Adult Male. Plate CCCLXXXI. Fig. 1.

Bill about the length of the head, much higher than broad at the
base, somewhat conical, compressed, rounded at the tip. Upper
mandible with the dorsal line sloping, the ridge broad and flattened at
the base, narrowed towards the unguis, which is roundish and very
convex, the edges beset with compressed, hard teeth-like lamellæ,
their outline ascending and slightly arched; lower mandible
ascending, nearly straight, the angle long and of moderate length,
the dorsal line beyond it convex, the sides erect, and beset with
lamellæ; similar to those of the upper, but more numerous, the
unguis obovate and very convex. Nasal groove oblong, parallel to
the ridge, filled by the soft membrane of the bill; nostrils medial,
lateral, longitudinal, narrow-elliptical, open, pervious.
Head of moderate size, oblong, compressed. Neck rather long and
slender. Body full, slightly depressed. Feet rather short, strong,
placed about the centre of the body; legs bare a little above the joint;
tarsus rather short, strong, a little compressed, covered all round
with hexagonal, reticulated scales, which are smaller behind; hind
toe very small, with a narrow membrane; third toe longest, fourth
considerably shorter, but longer than the second; all the toes
reticulated above at the base, but with narrow transverse scutella
towards the end; the three anterior connected by a reticulated
membrane, the outer having a thick margin, the inner with the margin
extended into a two-lobed web. Claws small, arched, rather
compressed, obtuse, that of the middle toe bent obliquely outwards,
and depressed, with a curved edge.
Plumage close, full, compact above, blended beneath, as well as on
the head and neck, on the latter of which it is disposed in longitudinal
bands, separated by narrow grooves; the feathers of the lateral parts
small and narrow, of the back ovato-oblong, and abruptly rounded, of
the lower parts curved and oblong. Wings rather long, broad;
primaries strong, incurved, broad, towards the end tapering, the
second longest, but only a quarter of an inch longer than the first,
which scarcely exceeds the third; the first and second sinuate on the
inner web, the second and third on the outer. Secondaries long, very
broad, rounded, the inner curved outwards. Tail very short, rounded,
of sixteen broad rounded feathers.
Bill carmine-red, the unguis of both mandibles white, their edges
black. Iris light brown. Feet dull lake, claws brownish-black. The
general colour of the plumage is pure white; the fore part of the head
tinged with yellowish-red; the primaries brownish-grey, towards the
end blackish-brown, their shafts white unless toward the end.
Length to end of tail 31 3/4 inches, to end of claws 33 1/2, to end of
wings 31 3/4, to carpus 14; extent of wings 62; wing from flexure
19 1/2; tail 6 1/4; bill along the ridge 2 5/8, along the edge of lower
mandible 3 1/4; bare part of tibia 3/4; tarsus 3 5/8; hind toe 1/2, its claw
4 1/2/ ; middle toe 3, its claw 4/12. Weight 6 3/4 lb.
12

Young Female, in first winter. Plate CCCLXXXI. Fig. 2.

The colours of the young bird, in its first plumage, are unknown; but
in its second plumage, in autumn and winter, it presents the
appearance exhibited in the plate. The bill is pale flesh-colour, its
edges black, and the unguis bluish-white; the feet flesh-colour, the
claws dusky. The head and upper part of the neck are white, tinged
above with grey, the lower part of the neck all round, the fore part of
the back, the scapulars, the fore part of the breast, and the sides,
blackish-grey; paler beneath. The hind part of the back and the
upper tail-coverts, are ash-grey; as are the wing-coverts; but the
secondary coverts are greyish-black in the middle; and all the quills
are of that colour, the secondaries margined with greyish-white; the
tail-feathers dusky-grey, broadly margined with greyish-white. The
dark colour of the fore part of the breast gradually fades into greyish-
white, which is the colour of the other inferior parts, excepting the
axillar feathers, and some of the lower wing-coverts, which are white.
Length of an individual in this plumage, kept four years, to end of tail
26 inches, to end of claws 25; extent of wings 55; bill along the ridge
2 1/4, from frontal angle 2 1/2; tarsus 2 7 1/2/12; hind toe 6/12, its claw
4 1/2/12; middle toe 2 1/4, its claw 4/12. Weight 2 lb. 13 oz. The bird
very poor.
In an adult male preserved in spirits, the roof of the mouth is
moderately concave, with five series of strong conical papillæ
directed backwards. The posterior aperture of the nares is linear,
margined with two series of extremely slender papillæ. The marginal
lamellæ of the upper mandible are 25, of the lower about 45. The
tongue is 2 inches 5 twelfths long, nearly cylindrical, with strong
pointed papillæ at the base, and on each side a series of flattened,
sharp lamellæ, directed backwards, together with very numerous
bristle-like filaments. It is fleshy, has a soft prominent pad at the base
above, and towards the end has a median groove, the point rounded
thin, and horny. The œsophagus; which is 17 inches long, has a
diameter of 9 twelfths at the upper part, and at the lower part of the
neck is dilated to 1 inch. The proventricular glands are cylindrical,
simple, and arranged in a belt nearly 1 inch in breadth. The other
parts were removed.
The reddish tint on the head affords no indication of the age of the
bird, some individuals of all ages having that part pure white, while
others have it rusty. The same remark applies to our two Swans.
 SHARP-TAILED GROUS.

Tetrao Phasianellus, Linn.

PLATE CCCLXXXII. Male and Female.

This is another species of our birds with the habits of which I am

entirely unacquainted. Dr Richardson’s account of it is as follows:
—“The northern limits of the range of the Sharp-tailed Grous is Great
Slave Lake, in the sixty-first parallel; and its most southern recorded
station is in latitude 41°, on the Missouri. It abounds on the outskirts
of the Saskatchewan plains, and is found throughout the woody
districts of the Fur Countries, haunting open glades or low thickets
on the borders of lakes, particularly in the neighbourhood of the
trading paths, where the forests have been partially cleared. In
winter it perches generally on trees, in summer is much on the
ground; in both seasons assembling in coveys of from ten to sixteen.
Early in spring, a family of these birds select a level spot, whereon
they meet every morning, and run round in a circle of fifteen or
twenty feet in diameter, so that the grass is worn quite bare. When
any one approaches the circle, the birds squat close to the ground,
but in a short time stretch out their necks to survey the intruder; and,
if they are not scared by a nearer advance, soon resume their
circular course, some running to the right, others to the left, meeting
and crossing each other. These “Partridge dances” last for a month
or more, or until the hens begin to hatch. When the Sharp-tailed
Grous are put up, they rise with the usual whirring noise, and alight
again at the distance of a few hundred yards, either on the ground,
or on the upper branches of a tree. Before the cock quits his perch,
he utters repeatedly the cry of cuck, cuck, cuck. In winter they roost
in the snow like the Willow Grous, and they can make their way
through the loose wreaths with ease. They feed on the buds and
sprouts of the Betula glandulosa, of various willows, and of the
aspen and larch; and in autumn on berries. Mr Hutchins says that
the hen lays thirteen white eggs with coloured spots early in June;
the nest being placed on the ground and formed of grass, lined with
feathers.”
Dr Townsend informs me that while crossing the north branch of the
Platte (Lorimie’s Fork), he found this species breeding, and that as
an article of food it proved to be a very well-flavoured and plump
bird, considerably superior to any of the other larger species that
occur in the United States.

Tetrao Phasianellus, Linn. Syst. Nat. vol. i. p. 273.—Lath. Ind. Ornith. vol.
ii. p. 635.—Ch. Bonaparte, Synopsis of Birds of United States, p. 127.
Tetrao Phasianellus, Sharp-tailed Grous, Ch. Bonaparte, Amer. Ornith.
vol. iii. p. 37, pl. 19.
Tetrao (centrocercus) Phasianellus, Swains. Sharp-tailed Grous,
Richards. and Swains. Fauna Bor.-Amer. vol. ii. p. 361.
Sharp-tailed Grous, Nuttall, Manual, vol. i. p. 669.

Adult Male. Plate CCCLXXXII. Fig. 1.

Bill short, strong, as broad as high; upper mandible with the dorsal
line arcuato-declinate, the ridge narrow at the base on account of the
great extent of the nasal sinus, which is feathered, the sides convex
toward the end, the edges overlapping and thin, the tip declinate and
blunt, but thin-edged; lower mandible with the angle of moderate
length and width, the dorsal line ascending and convex, the edges
sharp and inclinate, the tip obtuse.
Head rather small, oblong; neck of moderate length; body full. Feet
rather short, stout; tarsus roundish, feathered, bare and reticulated
behind. Toes of moderate size, with numerous scutella above, but
covered over at the base by the hair-like feathers which grow from
the sides and the intervening basal membranes, laterally pectinate
with long slender projecting flattened scales; first toe small, second a
little longer than fourth, third much longer. Claws slender, arched,
moderately compressed, rather obtuse; that of the third toe with the
inner edge dilated.
Plumage dense, soft, rather compact, the feathers in general broadly
ovate; those on the head and upper part of the neck short, but some
on the upper and hind part of the former elongated and forming a
slight crest. There is a papillate coloured membrane over the eye, as
in the other species; and on each side of the neck is a large bare
space, concealed by the plumage, which I have no doubt is inflated,
as in Tetrao Cupido and T. Urophasianus, during the love season.
Wings rather short, concave, much rounded; the primaries stiff and
very narrow, so as to leave large intervals when the wing is
extended; the third quill longest, the fourth next, the second shorter
than the fifth, the sixth longer than the first. Tail short, much
graduated, of sixteen feathers, of which the lateral are three inches
shorter than the central; all the feathers are more or less concave,
excepting the two middle worn along the inner edge, obliquely and
abruptly terminated, the two middle projecting an inch beyond the
next.
Bill dusky above, brown beneath; iris light hazel; superciliary
membrane vermilion; toes brownish-grey, claws brownish-black. The
upper parts are variegated with light red or brownish-orange,
brownish-black and white; the black occupying the central part of the
feathers, the light red forming angular processes from the margin,
generally dotted with black, and a lighter bar near the end; the white
being in terminal, triangular, or guttiform spots on the scapulars and
wing-coverts. The alula, primary coverts, secondary coverts, and
quills are greyish-brown, the coverts spotted and tipped with white;
the primaries with white spots on the outer web, the inner tipped with
white, as are all the secondaries, of which the outer have two bars of
white spots, and the inner are coloured like the back. The tail is
white, at the base variegated, and the two middle feathers like the
back. Loral space, and a line behind the eye, white; a dusky streak
beneath the eye, succeeded by a light coloured one. The throat is
reddish-white, with some dusky spots; the fore part and sides of the
neck barred with dusky and reddish-white: on the lower part of the
neck and fore part of the breast, the dusky bars become first curved,
and then arrow-shaped, and so continue narrowing on the hind part
of the breast, and part of the sides, of which the upper portion is
barred; the abdomen, lower tail-coverts, axillar feathers, and most of
the lower wing-coverts, white. The hair-like feathers of the tarsi are
light brownish-grey, faintly barred with greyish-white.
Length to end of tail 17 1/2 inches, to end of wings 14, to end of
claws 17; extent of wings 23; wing from flexure 8 1/4, tail 4 1/2; bill
along the ridge 10 1/2/12, along the edge of lower mandible 1 1 1/2/12;
1/2 1/2
tarsus 1 7 /12; hind toe 6/12, its claw 6/12; middle toe 1 7 /12, its
claw 7/12.

Adult Female. Plate CCCLXXXII. Fig. 2.

The Female is considerably smaller, but is coloured like the male,
the tints being duller.
 LONG-EARED OWL.

Strix otus, Linn.

PLATE CCCLXXXIII. Male.

This Owl is much more abundant in our Middle and Eastern Atlantic
Districts than in the Southern or Western parts. My friend Dr
Bachman has never observed it in South Carolina; nor have I met
with it in Louisiana, or any where on the Mississippi below the
junction of the Ohio. It is not very rare in the upper parts of Indiana,
Illinois, Ohio, and Kentucky, wherever the country is well wooded. In
the Barrens of Kentucky its predilection for woods is rendered
apparent by its not being found elsewhere than in the “Groves;” and
it would seem that it very rarely extends its search for food beyond
the skirts of those delightful retreats. In Pennsylvania, and elsewhere
to the eastward, I have found it most numerous on or near the banks
of our numerous clear mountain streams, where, during the day, it is
not uncommon to see it perched on the top of a low bush or fir. At
such times it stands with the body erect, but the tarsi bent and
resting on a branch, as is the manner of almost all our Owls. The
head then seems the largest part, the body being much more
slender than it is usually represented. Now and then it raises itself
and stands with its legs and neck extended, as if the better to mark
the approach of an intruder. Its eyes, which were closed when it was
first observed, are opened on the least noise, and it seems to squint
at you in a most grotesque manner, although it is not difficult to