Scientometric portrait of Dr. Atta-ur-Rahman.
Anjum, Manzoor Ahmad Khan ; Ahmad, Munir
Introduction
Bibliometrics is a word that means "the more that is published
on a topic, the more important the topic is in terms of money and energy
being used" (Jaing, 2003).
The terms bibliometrics by Pritchard and 'Naukometriya'
(the Russian for 'Scientometrics') by Nalimov & Mulchenko
were coined simultaneously in 1969 while Narin (1976) used the term
'Evaluative bibliometrics' to denote the use of bibliometric
techniques, especially publication and citation analysis in the
assessment of a scientific creativity.
The anyhow fuzzy borderlines between the two specialties almost
vanished during the last three decades and nowadays both terms are used
almost as synonyms. Instead, the field informetrics took the place of
the originally broader specialty bibliometrics (Glanzel, 2003).
Bbibliometrics is not only the term that is used to refer to the
quantitative study of document-related processes. Informatics and
librametry may be defined in similar ways; scientometrics,
technometrics, sociometrics and econometrics are fields that overlap
with bibliometrics to greater or lesser extent (in the sense either that
similar methods are used, or that related processes are studied); and
webrometrics and cybermetrics are new areas that focus specifically on
the communication of information in electronic form (UCLA Graduate
School).
Kalyane and Kalyane (1993) for the first time used the phrase
'Scientometric Portrait' to carry out bio-bibliometric studies
on scientists while Sinha & Bhatnagar (1980) and Sinha & Ullah
(1994) used the term 'Information profile' for such studies
while Sen (1995) proposed the term 'Microbibliometrics' for
the studies on individual scientists in IASLIC conference (1994)'
Recently the term 'Bio-bibliometrics' is being used for a
method of retrieving and visualizing biological information (Stapley
& Benoit, 2000) while Koganurmath, et al. (2003) have suggested that
'Scientometric portrait' is the appropriate phrase for the
studies on scientists and 'Informetric portrait' for the
studies on researchers in other disciplines such as arts, humanities and
social sciences.
Biographical Sketch
Professor Dr. Atta-ur-Rahman an outstanding academician and one of
the leading scientists in Pakistan completed his Masters in Organic
Chemistry from the University of Karachi in 1964 and obtained his PhD
from Cambridge University in 1968, where he later on had the rare
distinction of being appointed as Don at Kings College, Cambridge
(1969-1973) and D.A.A.D. Fellow of University of Tuebingen, Germany in
1979. He is also the only scientist from the Pakistan, other than the
late Prof. Abdul Salam (Nobel Laureate), who has been awarded the
prestigious degree of Doctor of Science (ScD) by Cambridge University.
Three Pakistani Universities, Sir Syed Engineering University (2003),
Gomal University (2004) and Karachi University (2005) each awarded him
D.Sc. degree
He is internationally renowned in the field of Natural Product
Chemistry. He has hundreds of publications to his credit including 15
Patents, 94 Books, 59 Chapters in Books published by major US and
European presses while more than 70 students have completed Ph.D
researches under his supervision.
He is an eminent writer and the level of his writings can be judged
from the fact that his first book "Biosynthesis of Indole
Alkaloids" was published by Oxford University Press, England as
Vol. 7 of their prestigious "International Series of Monographs in
Chemistry' in 1983 while another book "Nuclear Magnetic
Resonance Spectroscopy" is considered to be the first text book to
have a detailed discussion on 2D-NMR spectroscopy. Its success in USA
and Europe prompted it to be translated into Japanese language by Prof.
H. Hirota from Tokyo University and Prof. Motoo Tori from Tokushima
Bunri University. Another title "Stereoselective Synthesis in
Organic Chemistry", published by Springer-Verlag, Germany was
appreciated by the Nobel Laureate Sir D.H.R. Barton, who wrote its
foreword and called it "a monumental tome."
The Government of Pakistan has conferred four civil awards on him
in recognition of his eminent contributions in the field of Organic
Chemistry. He has also won several national and international prizes. He
is the first scientist from the Islamic World to have received the
prestigious UNESCO Science Prize (1999) in the 35 year old history of
the award. He has secured numerous other national and international
prizes and awards including the Federation of Asian Chemical Societies
Award (Hiroshima, Japan, 1997), the ECO Prize (2000), ISESCO Prize
(2001), the Islamic Organization Prize by Government of Kuwait (1988),
the First Prize at the 6th Khwrazmi Festival by the President of Iran
(1993), the FPCCI Prize for Technological Innovation (1985), the
"Best Scientist of the Year" Award of the Government of
Pakistan (1986), and the Prime Minister's Gold Medal and Pakistan
Academy of Sciences-INFAQ Foundation Prize in Science (1995).
He is Fellow of three major international science academies and
Editor-in-Chief/Executive Editor of fifteen leading European Chemistry
journals. He is also the Editor of five book-series entitled
"Studies in Natural Product Chemistry", 32 volumes of which
have been published under his editorship during the last 14 years. He is
also editing "Frontiers in Medicinal Chemistry".,
"C-13-NMR of Natural Products", "Advances in Organic
Chemistry", "Advances in Organic Synthesis" and
"Frontiers in Drug Design and Discovery".(Taken from
Dr.Atta-ur-Rahamn's Bio).
Study Objective
The prime purpose of the study is to document quantitatively the
publication productivity pattern of Dr. Atta-ur-Rahman and particularly
it highlights:
* Year-wise, quinquennium-wise and domain-wise productivity
* Domain-wise authorships and collaborative pattern
* Identify prominent collaborators
* Collaborator dynamics
* Mentor's authorship credibility
* Prominent, new and overlapping collaborators
* Core Channels of Communication and distribution of publications
among these channels and
* Bradford multiplier
* Geographical distribution of publications, and
* Documentation of keywords used in the titles.
Literature Review
Both terms bibliometrics and scientometrics are used for the study
of statistical analysis of scientific literature and to trace the origin
of statistical studies we have to go back about 46 years before the
coinage of these terms in early twenties of the twentieth century when
E. W. Hulme (1923) published his book "Statistical Bibliography in
Relation to the Growth of Modern Civilization."
Alfred J. Lotka (1926) conducted a study on the frequency
distribution of scientific productivity while the very next year Gross
and Gross (1927) conducted a citation-based study by examining 3633
citations and is considered to be the first citation analysis. In 1934,
Bradford conducted a study on the frequency distribution of papers over
journals while Zipf (1949) formulated an interesting law in
bibliometrics and quantitative linguistics for studying word frequency
in a text.
Until the early 60s these studies were not given much importance.
Glanzel (2003) identifies three reasons for this phenomenon.
1. These papers appeared when traditional methods of information
retrieval were still sufficient
2. They applied to different phenomena and the interrelation
between these laws which was not completely recognised; and
3. Financing systems for scientific research did not yet stand need
of quantitative or even sophisticated statistical methods.
Derek deSolla Price (1963) by analysing the system of science
communication laid down the foundation of modern research evaluation
techniques and paved a path for the modern scientometrics.
Mentionable efforts for the institutionalisation of the field are,
the launching of first international journal "Scientometrics"
by Tibor Braun in 1979 followed by the first international conference in
1983 (being held annually since then). The
bibliometricians/scientometricians contributed a number of books and
articles and developed complex models of scientific communication to
strengthen the foundation of the discipline. The bibliometrics continue
its journey passing through different phases and as a result of these
efforts "Baby Scientometrics" in the words of (Glazel, 2003)
evolve into a distinct scientific discipline with a specific research
profile, several subfields and the corresponding scientific
communication structures.
Some biographical and bio-bibliometric studies of individuals have
been carried out occasionally at the time of retirement or paying homage
to an individual after death. For some noted individuals their
contributions are highlighted in the obituary column of professional
journals (Koganurmath, 2003).
Hirsch (2005) for the quantification of scientific output of
individual scientific authors suggested the h-index, also known as the
Hirsch Number which is based on the citations each article (paper) of an
author gets. This number has several advantages over other criteria.
H-index has been suggested for use in academic promotions, tenure, grant
funding, and prediction of winning of the Nobel Prize.
Recently individual scientists including the Nobel Laureates are
becoming the focus of scientometric studies rather than gross
statistical "macro" data (Schubert and Glanzel, 1992). Among a
number of scientometric studies on Nobel Laureates few are:
Scientometric portrait of Nobel Lauriat Leland Dr. C.V. Raman
(Kademani, Kalyane & Kademani, 1994), Barbara McClintock: (Kalyane
and Kademani, 1997), S. Chandrasekhar (Gupta, 1983), Dorothy Crowfoot
Hodgkin (Kademani, Kalyane & Jange, 1999), Ahmed Hassan Zewail
(Kademani, Kalyane & Kumar, 2001), Harold W. Kroto (Kademani,
Kalyane & Kumar, 2002), Pierre--Gilles de Gennes (Kalyane & Sen,
1996), Wolfgang Ketterle (Koganuramath, et al., 2003) and H. Hartwell
(Angadi, et al., 2004).
Besides Nobel Laureates there are numerous scientometric studies on
other scientists in various disciplines, the reference is made to some
of such studies as:
The research by Kalyane & Kalyane (1993), (Kademani, Kalyane
& Balakrishnan (1994), Kalyane (1995), Prpic (1996), Kalyane &
Sen (1996), Hawkins (2001), Kalyane, Prakasan and Kumar (2001), Swarna,
Kalyane and Kumar (2002), Kademani, et al., (2005), Kademani, et al.
(2006), Sangum, Savanur and Sarathi (2006), Sangam and Savanur (2006),
Tiew (2006), van Raan (2006), (Koley & Sen 2006), Anuradha & Urs
(2007), Fred Y. Ye (2007), Sagar, Kademani and Kumar (2007), Leydesdorff
& Meyer (2007), Ocholla & Ocholla (2007), Pouris (2007) and
Yazit & Zainab (2007).
Few examples of bibliometric/citation studies from Pakistan are:
Kousar & Mahmood (2010). Naseer & Mahmood (2009), Mahmood &
Rehman (2009), Javed & Shah (2008), Ullah, Butt & Haroon (2008),
Ullah (2006), Sharif & Mahmood (2004), Majid (1995, 2000), Anwar and
Saeed (1999), Khan and Samdani (1997) and Mahmood (1996).
The bibliometricians, scientometricians and information specialists
also contributed a number of books on theory and applications of the
discipline. A few examples of such publications are:
Introduction to informetrics: quantitative methods in library,
documentation and information science (Egghe and Rousseau, 1990),
Handbook of quantitative studies of science & technology (van Raan,
1988), Bibliometric mapping as a science policy and research management
tool (Noyons, 1999), The challenge of scientometrics: The development,
measurement and self-organization of scientific communications
(Leydesdorff, 1995) and Scholarly communication and bibliometrics
(Borgman, ed. 1990).
Among a large number of useful web-sites providing information on
different aspects of bibliometrics few are:
* Applications in Teaching Bibliometrics by Sara von
Ungern-Sternberg. htp://www.ifla.org/IV/ifla61/61-ungs.htm
* Bibliometric Mapping by the Centre for Science and Technology
Studies (CWTS) at Leiden University in the Netherlands.
http://sahara.fsw.leidenuniv.nl/ed/projects.html
* BIRD: Bibliometric Retrieval of Documents, from the National
Research Council CanadaInstitute for Information Technology.
http://ai.iit.nrc.ca/II public/WebBird/index.html
* BIRD Resources: Bibliometric Systems. A list of bibliometric
systems, projects and links. http://ai.iit.nrc.ca/II
public/WebBird/bibliometric.html
* Bibliometrics, Scientometrics & Informetrics by Luc Quoniam
http://crrm.univ-mrs.fr/vl/metricts.html
Methodology
On critical study of the list down loaded from the web, it was
observed that there are certain duplicate titles in the list. After
dropping duplicate titles the list counts 766 publications which are
considered for study purpose.
The study identifies year, quinquennium and domain-wise
productivity and collaborativeships, collaborative pattern,
mentor's authorship credibility, individual collaborator dynamics,
channels of communication used and distribution of publications among
channels and geographical distribution of publications. Further, the
study find out prominent collaborators, the most productive period, top
ranking journals, publication density and concentration, Bradford
multiplier and high frequency words used in the titles.
Data Analysis & Discussion
The contribution of 766 publications during 1966-2007 by the mentor
were analyzed year, quinquennium and domain-wise, author-wise
authorships credits, mentor's authorship credibility, channels of
communication used, countries of productivity and keywords used in the
titles.
1. Productivity
The productivity can be divided into; year-wise, quinquennium-wise
and domain-wise and are discussed as under:
1.1 Year-wise Productivity
Table-1 describes year-wise contribution of 766 publications by
thementor from 1966-June 2007. He contributed 1 (0.13 %) publication in
each year 1966, 1968 and 1969 while maximum 67 (8.75 %) publications in
the year 2005. Still 4 (0.52 %) publications are in the press while 8
(1.04 %) have been submitted for acceptance. In his 42 years of research
career 1970 is the only year when he made no contribution.
The contribution of 222 (28.98 %) publications during five high
productive years (1988, 2002, 2003, 2004 and 2005) indicates that more
than one-fourth productivity is the result of less than one-eighth
period of productive years (42 years) while 50 % productivity in ten
high productive years indicates that half of the total productivity is
the result of less than one-fourth of the entire period (1966-2007) of
productivity. The productivity of 624 (81 %) publications in 20 high
productive years indicates that more than four-fifth of toal
productivity is the result of less than fifty percent of total period of
productivity. It is obvious from the above discussion that in least 22
productive years, the productivity is less than one-fifth of the entire
productivity from 1966-2007. By dividing total period of productivity
(42 years) into three clusters of 14 years each, we find that in the
first cluster of 14 years (1966-1979) the productivity is only 47 (6.14
%) publications. In the next cluster (1980- 1993) the productivity is
301 (39.3 %) while in the last cluster of 14 years from 19942007, he
contributed 418 (54.57 %) publications. It is obvious from the above
discussion that the productivity (39.3 %) in the second cluster and
(54.57 %) in the third is more than six-times and about nine-times
respectively as compared with the first cluster of 14 years of
productivity.
In case of decade-wise productivity it is 23 (3.00 %) in the first
decade (1966-75), 113 (14.75 %) in the 2nd decade (1976-85), 268 (34.99
%) in the third (1986-95) while in the fourth decade (1996-05) it is 316
(41.25 %). The decade-wise analysis of productivity indicates that only
3 % of entire productivity is during the 1st decade, about one-seventh
in the 2nd decade, about one-third in the third while more than
two-fifth of entire productivity is in the last decade. Moreover, the
collective productivity during the third & the fourth decades is
more than three-fourth (76.24 %) of the entire productivity.
The publication productivity coefficient .69 indicates his higher
productivity period just after 50 percentile age of his research career
under consideration.
1.2 Quinquennium-wise Productivity
Table-2 describes quinquennium-wise productivity which consists
over nine quinquenniums from 1966-2007. As the productivity in the 9th
quinquennium is only of two years, thus it is not reflecting the exact
productivity for the complete 9th quinquennium (2006-10).
The productivity in the 8th quinquennium at its peak point is even
more than the collective productivity of first four quinquenniums
(I-IV). The productivity from 1st to 5th quinquennium remains increasing
while decreases in the sixth and seventh quinquenniums. The collective
productivity (49.74 %) in three quinquenniums (5th to 7th) is nearly
equal as compared with the collective productivity of remaining six
quinquenniums (1st- 4th, 8th & 9th) irrespective the decade with
maximum productivity (8th) is also included in these six quinquenniums.
1.3 Domain-wise Productivity
The entire productivity in various domains is NP 90 (11.75 %),
NP-syn & NP-x-ray each 9 (1.18 %), NP-iso 423 (55.22 %), NP-nmr 14
(1.93 %), SY 132 (17.23 %), SP 27 (3.53 %), AC 8 (1.04 %), MC 24 (3.13
%) and Misc. 30 (3.92 %). Domain-wise detail of 83 (10.83 %)
single-authored contribution is NP 28 (3.66 %), NP-syn 9 (1.18 %),
NP-iso 13 (1.7 %), NP-nmr and AC each 2 (0.26 %), SY 16 (2.09 %), MC 6
(0.78 %), SP 4 (0.52 %) and Misc. 3 (0.39 %) while collaborative
productivity in various domains is NP 62 (8.09 %), NP-iso 410 (53.53 %),
NP-x-ray 9 (1.18 %), NP-nmr 12 (1.57 %), SY 116 (15.14 %), MC 18 (2.35
%), SP 23 (3.0 %), AC 6 (0.78.%) and Misc. 27 ( 3.53 %).
The single-authored productivity (3.66 %) in the domain of NP is
more than all other categories (211, 13, and 21 -authored) while
five-authored productivity (85) in the domain NP-iso is the highest
followed by six-authored (77), four-authored (71) and seven-authored
(52).
Under the domain of NP-x-ray the maximum productivity is by
6-authored while in case of NP-nmr 2-authored contribution is the
highest followed by each 3, 6, single and each five and seven-authored
respectively. Under the domain SY two-authored productivity is the
highest (39) followed by three-authored (18) and in case of domain AC
single and 6-authored productivity is the same and the highest 2 (0.26
%).
Table-4a provides the detail of 3214 (97.48 %) collaborative
authorships out of total 3297 authorships. Among these 3214
collaborativeships 274 (8.53 %) are two-authored, 285 (8.87 %)
three-authored, 400 (12.45 %) four-authored, 550 (17.11 %)
five-authored, 672 (20.91 %) six-authored, 476 (14.81 %) seven-authored,
208 (6.47%) eight-authored, 162 (5.04 %) nine-authored, 120 (3.73 %)
ten-authored, 33 (1.03 %) eleven-authored, 13 (0.4 %) thirteen-authored
and 21 (0.65 %) collaborative authorships are twenty-one-authored.
The number of collaborationships is the highest 672 (20.91 %) in
case of six-authored productivity followed by five-authored contribution
550 (17.11 %). The contribution of more than 80% coauthorships is by six
high productive categories (2 to 7-authored) while the remaining six
categories (8 to11, 13 and 21-authored) contributed less than 20 %
collaborativeships.
The number of collaborativeships from one to six-authored
productivity remains increasing and afterwards decreasing till
13-authored productivity which indicates that in case of 1-6-authored
productivity, the relationship between number of collaborativeships and
category of productivity is directly proportional while from 7 to
13-authored productivity this relationship is inversely proportional.
The authorship per paper is 4.3.
Table 4b provides the detail of 2531 collaborations made by
co-authors. The most prolific collaborator contributed 398 (15.73 %)
authorships while 250 collaborators contributed 250 (9.88 %)
co-authorships one each.
The contribution of 398 (15.73 %) collaborativeships by one
collaborator indicates that the credit of one-seventh of total
co-authorships goes to only one collaborator. The contribution of 846
(33.43 %) co-authorships out of total 2531 by only 18 out of total 547
collaborators indicates that 3.3 % of total collaborators contributed
one-third of the total collaborativeships while only 57 co-authors
contributed 50 % of the total collaborativeships.
It is evident from the data that the contribution of 50 %
collaborativeships only by 57 reseachers is equal to the remaining 490
collaborators while the contribution of 94.47 % collaborativeships by
only 92 collaborators indicates that collaborativeships contribution
exceeds the general rule of 80/20.
2.1 Year-wise Collaborativeships
Table-4c describes year-wise contribution of co-authors. More than
three-fifth (61.52 %) of the total collaborativeships is the result of
ten most productive years (1988, 1991, 1995, 1998 and 2001-2006) while
more than four-fifth (88.27 %) of the entire collaborativeships is the
result of 20 most productive years. It is obvious from the data that the
contribution of more than 80 % of collaborativeships is in 20 years
while in the remaining 22 years these are only 12 %.
2.2 Quinquennium-wise Collaborativeships
Table-4d about quinquennium-wise collaborationships indicates that
the highest number of collaborationships 950 (37.53 %) are in the 8th
quinquennium (2001-05) followed by 401 (15.84 %) in the 6th quinquennium
(1991-95).
3. Mentor's Authorship Credibility
The credit of contributing 766 out of 3297 authorships goes to the
mentor. Table 5 describes his authorship credibility. The credibility of
444 (57.96 %) publications as first author and 74 (9.66 %) as second
author indicates that being the first or the second author he is mainly
responsible for the contents and productivity of 67.62 % publications.
In case of 86.55 % publications his authorship credibility varies from 1
to 5 while in case of only 13.45 % publications the authorship
credibility is either seventh or beyond.
4. Collaborator Dynamics
Individual author's domain-wise profile of productivity is
presented in table-6 (See Appendix A). The 547 authors contributed 2531
(76.77 %) collaborative authorships with the mentor. The top
collaborator has 398 (12.07 %) co-authorships while coauthorships
contributed by 296 authors varies from 43 (1.3 %) to 2(.06 %). The
remaining 250 authors contributed 1(.03 %) authorship each.
4.1 Year-wise Collaborator Dynamics
During the 42 years of mentor's productivity (1966-2007), the
number of colaborators varies in different years. There are only three
authors including the mentor in the year of the first publication (1966)
and maximum number of co-authors are 318 (12.56 %) in the year 2005.
In the year 1966 all collaborators are new while in the years 1967,
1968, 1971,1975,1978, 1979 and 1981 all collaborators are those who
continue to collaborate from previous years. Maximum number of new and
overlapping collaborators at one time are 55 (2.17 %) and 263 (10.39 %)
in the year 2005 respectively while maximum number of collaborativeships
318 (12.56 %) at one time are also in the same year. The collaborators
joining the mentor for the first time contributed 369 (14.58 %)
co-authorships in 10 high collaborativeships years while in the same
period collaborators who continue to collaborate contributed 1209 (47.77
%) collaborativeships. It is evident from the above discussion that the
number of overlapping collaborators is four-times than the new
collaborators in high ten years of collaborativeships. It can be
inferred from the above ratio of new comers and overlapping
collaborators that the co-authors once join the group seems to be
satisfied with their output and group.
4.2 Quinquennium-wise Collaborator Dynamics
During the 9 quinquenniums from (1966-2007) 2531 reseachers
collaborate with the mentor. During the three quinquenniums (6th to 8th)
371(67.82 %) new collaborators join the mentor while during the same
period (6th & 8th quinquenniums) the overlapping collaborators are
69 %. It is evident from the data that with the passage of time the
number of collaborators in each quinquennium increased.
5. Channels of Communication:
The mentor used 113 channels of communication to publish 756 out of
total 766 publications in which 106 (13.84 %) are published locally
while 660 (86.16 %) from abroad. For the remaining ten titles the names
of publishers are not mentioned in the list provided by the mentor.
Channel-wise scattering of publications is depicted in the table-8 as
below.
The Photochemistry by publishing 93 (12.14 %) titles is at the top
followed by Elsevier Science Publishers and J. Nat. Prod 56 (7.31 %)
each. Fourteen channels each publish 2 (.26 %) titles while 55 channels
of communication (12 local and 43 foreign) publish only 1 (.13 %) title
each. It is interesting to note that among the most prolific publishers,
the top seven belongs to foreign countries.
The publication of 346 (45.17 %) titles by 7 top publishers
indicates that one-sixteenth numbers of publishers publish more than
forty percent of titles and all are foreign. The publication of 413
(53.9 %) titles in ten channels of communication indicates that less
than one-eleventh numbers of channels publish more than fifty percent
titles and among these ten publishers, local is only one. It is evident
from the above discussion that 90% channels of communication used among
top ten are foreign.
The publication density in this case is 6.69, (the ratio of total
number of papers published to the total number of channels in which the
papers were publishedwhile publication concentration is 7.96 (as the
ratio in percentage of the journals containing half of the papers
published to the total number of journals in which those papers were
published during the period under study) (Vinkler (1990).
6. Bradford Distribution:
Dr. Atta-ur-Rahman contributed 766 publications during the entire
period of productivity (1966- June 2007). For the ten publications the
names of channels of communication are not mentioned. To test for the
remaining 756 publications whether his contribution follows Bradford
distribution or not, the productivity is divided into three zones each
having approximately 252 papers.
The first 4 channels published 253 titles, the next 16 published
250 while in case of 3 rd zone 64 channels published 253 publications.
The below table provides zone-wise distribution of publications and
journals.
Bradford multiplier is 4 in this case. According to this multiplier
the number of publications in the third zone should be 4x4x4 = 64 which
is exactly the same as actual number 64. Thus the data follows the
Bradford Law of distribution, Garfield, E. (1979).
Zones Papers Journals
1st 253 4
2nd 250 16
3rd 253 64
7. Geographical Distribution of Publications
The table below explains countrywise distribution of the
publications. The publishers from 23 countries published 766 titles. UK
is at the top by publishing 220 (28.72 %) titles followed by USA 131
(17.1 %) and Pakistan 106 (13.84 %)., Germany 91 (11.88 %), The
Netherlands 89 (11.62 %), Japan 57 (7.41 %) while 11 countries publish 1
(0.13 %) title each. The numbers of locally published titles are 106
(13.84 %) while the numbers of titles published abroad are 660 (86.16
%). The top seven countries published 95.14 % titles and the titles
published in developing countries is about 16 % as compared with the
developed world.
8. Keywords Tomography:
Titles of publications convey precisely the thought contents of
publications. Therefore, if a word occurs more frequently than expected
to be occurred, then it reflects the emphasis given by the author about
the domain of his research (Angadi, et. al., 2006). The list of keywords
with frequencies in parenthesis appeared in the titles of publications
is provided in descending order as under. The words without frequencies
are those which appear once in the titles.
Natural (84), Synthesis (77), Products (74), Chemistry (69),
Isolation (68), Natural Products (54), Alkaloids (53), Studies (45), New
(42), Structure (41), Natural Products Chemistry (36), Bioactive Natural
Products (32), Alkaloid (29), Constituents (26), Novel (25), Steroidal
Alkaloids (26), Recent (22), Rhazya stricta (22), Stereoselective ( 22),
Microbial Transformation (21), Buxus papillosa (20), Chemical
Constituents (19), Vinblastine (19), Derivatives (18), Synthetic (18),
Medicinal Plants (17), New Steroidal Alkaloids (16), Structural Studies
(16), Bioactive (15), Chemists (15), Publications (15), Their (15),
Atharanthus roseus (14), Activity (14), Directory (14), OIC Members
(14), Sarcococca saligna (14), Scientific (14), States (14),Some (13),
Structure Elucidation (13), Leaves of Buxus papillosa (12), Structural
(12), Frontiers (11), Inhibitors (11 ), Syntheses (11), Synthetic
Studies (11), Total (11), Antifungal (10), Inhibiting (10), Vincristine
(10), a-Carbolines (9), Crystal (9), Leaves of Rhazya stricta (9),
Medicinal (9), Reactions (9), Alstonia macrophylla (8), Buxus
sempervirens (8), Harmaline (8), Indigenous (8), Isolated (8), Leaves
(8), Pakistan (8), Tinospora malabarica (8), Withania coagulance (8),
13C-NMR (7), Antibacterial (7), Ervatamia coronaria (7), Inhibition (7),
Plants (7), Prolyl Endopeptidase (7), Structure and Chemistry (7),
Tyrosinase (7), Using (7), Withania somnifera (7), Acetylcholinesterase
(6), Compounds (6), Procedure (6), Rhizomes (6), Urease (6), Veratrum
album (6), Advances (5), Alstonia scholaris (5), Analogues (5),
Biotransformation (5), Butyrylcholinesterase (5), Characterization (5),
Delphinium denudalum (5), Elucidation (5), Fungal Transformation (5),
Indole Alkaloids (5), Inhibitory Activity (5), Microbial Transformations
(5), Nepalese Origin (5), New Cholinesterase (5), New Indole Alkaloid
(5), New Triterpenoidal Alkaloids (5), Nigella sativa (5), Nigellicine
(5), Phytochemical Studies (5), Seeds (5), Skimmia laureola (5),
Spectroscopy (5), Strictamine (5), Suregada multiflora (5),Transformed
Products (5),Triterpenoid (5), Withanolides (5), a-Glucosidase (4),
Amides (4), Anti-Inflammatory (4), Biological (4), Buxus hyrcana (4),
Coumarins (4), Diterpenoid (4), 11-Methoxyrutaecarpine (4), Fagonia
indica (4), Fumaria indica (4), Handbook of Natural Products Data (4),
Handbook (4), Indole (4), Iris bungei (4), Iris germanica (4), Leaves of
Catharanthus roseus (4), 2D NMR Techniques (4) 2D NMR Techniques (4),
Source (4), Leucosceptrum canum (4), Medicinal Plants of Pakistan (4),
Molecular (4), New Isoquinoline Alkaloid (4), New Withanolides (4),
Norditerpenoid Alkaloids (4), Organic (4), Petchia ceylanica (4),
Potential Biological Importance (4), Reduction (4), Rhazimol (4), Roots
of Buxus papillosa (4), Selected (4), Sphaeranthus indicus (4), Study
(4), Towards (4), Two (4), Vinrosidine (4), Alkaloidal (3), Anti
leukaemic Alkaloids (3), Anticancer Alkaloids (3), Anticonvulsant
Activities (3), Antioxidant (3), pproaches (3), Aqueous Fraction (3),
Bongardia chrysogonum (3), Buxus hildebrandtii (3), Catharanthine (3),
Cephalosporium aphidicola (3), Cholinesterase Inhibitory Activity (3),
16-epi-19S-Vindolinine (3), Conformational (3), Cyclization (3), Datura
fastuosa (3), Diterpenoids (3), Encyclopaedia (3), Fritillaria
imperialis (3), Fruits (3), Haplophyllum buxbaumii (3), Imides (3),
Inhibitory(3), Inhibitory Activity (3), Leaves of Buxus sempervirens
(3), Leucosceptrine (3), Magnetic (3), Medica (3), Method (3), Modern
(3), Moenjodaramine (3), Molecular Structure (3), New Indole Alkaloids
(3), New Natural Products (3), New Pregnane-Type Steroidal Alkaloid (3),
NMR Studies (3), Nnovel (3), Nuclear Magnetic Resonance (3), Nuclear
(3), Organic Chemistry (3), Partial (3), Planta Medica (3), Planta (3),
Quinoline Alkaloid (3), Relationship (3), Resonance (3), Roots of Buxus
sempervirens Roots of Delphinium denudatum (3), Saponins (3),
Semperviramidine (3), Sesquiterpene (3), Sesterterpenes (3), Sodium
Borohydride (3), Sophora griffithii (3), Spatoglossum variabile (3),
Spices (3), Structure-Activity (3), Tiliacora racemosa (3), Trends (3),
Triterpenes (3), Absolute (2), Allium (2), Alstonia species (2),
Alternative Method (2), Analytical Chemistry (2), Antihypertensive
Alkaloids (2), Antileukaemic (2), Arylnaphthalene Lignans (2),
Asymmetric Synthesis (2), Autocrine Inflammatory Mediator (2), Bacopa
monniera (2), Bioactive Constituents (2), Benzopyrone Derivatives (2),
Betula utilis (2), Bioactivities (2), Biodiversity (2), Biological
Evaluations (2), Biological Screening (2), Bisbenzylisoquinoline
Alkaloids (2), Botrytis cinerea (2), Bridged (2), Buxus longifolia(2),
Buxus sempervirens L. (2), Buxuspapilosa (2), Cadaba fruticosa (2),
Calcium Channel Blocking (2), Cell Suspension Culture (2),
Cholinesterase Inhibiting Withanolides (2), Cocculus hirsute (2),
Cocculus pendulus (2), Colchicum decaisnei (2), Complex Natural Products
(2), Configuration (2), Dihydrocleavamines (2), Delphinium nordhagenii
(2), Drug Design (2), Cytotoxic (2), Demethoxycarbonyldeoxyvinblastine
(2), Cunninghamella elegans (2), Design (2), Determination (2), Dimeric
Tropane Alkaloids (2), Diphenylbisbenzylisoquinoline Alkaloid (2),
Diterpene Lactones (2), Diterpenoid Alkaloids (2), Dynamics (2),
Economical (2), Efficient (2), Enamine (2), Erratum (2), Ervaticine (2),
Erythroxylum moonii (2), Essential (2), Ethanolic Extract (2), Ethers
(2), Evaluation (2), Facile (2), Field (2), Five New Peltogynoids (2),
Furanoid Diterpene (2), Furanoid (2), Further (2), Gomaline (2), Growth
(2), Halenia corniculata (2), Harappamine (2), Hecubine (2),
Hypoglycemic Activity (2), Identification (2),Imine-Enamine (2),
Immunomodulatory Properties (2), Indolic (2), Indolic Imides (2),
Inhibitor (2), Inhibitory Constituents (2), Intermediates (2), Isodon
rugosus (2), Isoflavonoid Glycosides (2), Karachic acid (2), Kinetics
(2), Lactones (2), Leaves of Alstonia macrophylla (2), Leaves of
Sarcococca oriacea (2), Legumes of Rhazya Stricta (2), Leontice
leontopetalum (2), Leuconollam sesquihydrate (2), Lindelofia stylosa
(2), Lupine Alkaloids (2), Marine Brown Alga (2), Marine Organisms (2),
Mestranol (2),Methods (2), Microbial (2), Microbial Metabolism (2),
Mixture (2), New Antioxidant (2), New Dihydroindole Alkaloid (2), New
Indolenine Alkaloid (2), New Isoflavone (2), New Theory of Memory (2),
Nigellimine (2), N-oxide (2), Oil (2), One step Synthesis (2), Oxindole
Alkaloid (2), Paeonia emodi (2), Papilamine (2), Partial Syntheses (2),
Pentacyclic Triterpenes (2), Pentacyclic (2), Perspectives (2),
Pharmacophores (2), Phosphodiesterase (2), Phytochemical (2), Potential
(2), Pregnane-Type Steroidal Alkaloids (2), Presence (2), Process (2),
Protecting Groups (2), Protoberberine Alkaloids (2), Pteleopsis
hylodendron (2), Quinovic Acid Glycosides (2), Rapid (2), Reactions of
Harmaline (2), Rearrangement (2), Recent (2), Recent Advances (2),
Recognition (2), Reductive (2), Relationship (2), Revisiting Diterpene
Lactones (2), Rhazimal (2), Rhazimine (2), Rhazya orientalis (2), Roots
of Rhazya stricta (2), Rosamine (2), Saponin (2), Sarcococca brevifolia
(2), Sarcococca hookeriana (2), Sesterterpene (2), Sodium Bromate (2),
Sodium Hydrogen Sulfite (2), Spectral Deductions (2), Spectroscopic (2),
Spectrum (2), Stereochemistry (2), Stricticine (2), Taxus wallichiana
Zucc. (2), Terminalia glaucescens (2), Trachelospermum jasminoides (2),
Triterpene (2), Triterpenodal Alkaloids (2), Triterpenoid Alkaloids (2),
Triterpenoids (2), Utilization (2), FS-1 Subfraction (2), Interleukin-8
(2), 1H/13C-NMR (2) (-)- Caryophyllene Oxide (2), (-)-Ambrox (2),
(+)-Androsta-1,4-Diene-3,17-Dione (2), (+)-Catharanthine (2),
(+)-Eburnamonine (2), (+)-Vincamine (2), 11-Methoxynauclefine (2),
11-Methoxynauclefine (2), 5-Disubstituted-1,3,4-Oxadiazoles (2).
(-) -Ambrox, (-) Pinene, (-)-Isolongifolol, (-)-isolongifolol,
(+)-16-Hydroxydihydrocleavamine, (+)-Adrenosterone,
(+)-Cycloisolongifol-5-ol, (+)-a- and a-Dihydrocleavamines,
(+)-Cycloisolongifol-5-beta-ol,
(+)-16-Methoxy-carbonyldihydrocleavamine, (+)-Dihydrocatharanthine,
(+)-di-OMethyl Syringaresinol, (+)-N-Formylharappamine, (+)-epi
-Ibogamine, (+)-Ibogamine, (+)-N-formylpapilicine,
(+)-N-Methyltiliamosine, \ (+)-N-Acetyl-N-dimethylcyclomicrobuxeine,
+)-Methifloramine, (+)-Scareolide, (1R,2S,5R)-(-)-Menthol,
(2,4,6-trihydroxyphenyl), (4 Hydroxyphenyl), (4R)-Thiazolidine
Carboxylic Acid, (D)-Pinene, (deacetylakuammiline), (R)-synephrine
hydrochloride, 1,2,3,6, 11-Hexahydro-3-oxoindolizino (8,7-b), 1,2
Dehydroaspidospermidine N-oxide, 1,5-Benzothiazepine Derivatives,
10,12,12-Tris(3,3-dimethylallyl)-6,7-Dihydroxy
-2,2,9-Trimethyl-1H-pyrano [2,3-b]antr-acen-5(12H)-one,
11Hydroxyepipachysamine-E, 11-methoxy Indoloquinolizidines,
11-Methoxy-5,6-dihydrosempervirine, 12-Epinapelline,
16-Hydroxydihydrocleavamines, 20-dihydrocondylocarpine,
16-Methoxycarbonydihydrocleavamine, 19, 19,20-E-Vallesamine,
19,20-Z-Vallesamine, 1D, 15 Acetoxydihydrocatharanthine,
1-Isopropenyl-3a,5a,5b,8,8,11a-hexamethylicosahydro-1H-cyclopenta[a]chrysen- 9-yl, 4-hydroxy-3methoxycinnamate, 20-Dimethylamino-3a,
a-methylamino-5a-pregnane 217a-Ethynylestradiol, 17
a-dimethoxy-5a-estra-1, 10a-Hydroxycolumbine, 7a-Hydroxyfrullanolide,
7-Hydroxy-4-Methyl-2H-Chromen-2-One, 17-Ethynel-3,
7-Hydroxy-4,5-Dimethyl-2H-Chromen-2,One2,
20-N-Ethyl-1,8,14-trihydroxy-16a,18-dimethoxylycoctonine, 15,
20-anhydrovinblastine, 2-Amino-2-Deoxy-D-Mannose,
2-Methoxy-1,2-dihydrorhazimine, 2-Methoxycarbonyl succinanilic acid,
2-Substituted 50,6-Dihydro-5-oxo-4H-1,3,4-oxadiazine-4-propanenitriles
and of Their Intermediates, 2-Substituted Analogues,
3-(2-Furanyl)-2-Propenoic Acid, 3-(2-Thienyl)-2-Propenoic Acid,
3-(3,7-Dimethylocta-2,6-dienyloxy)-1,8-dihydroxy-6-methyl-9,10-anthraquinone, 35 (10)-triene, 30-Acetoxy-Na-benzoylbuxidienine,
3-Acetoacetyl-7-Methylpyrano-[4,3-b]pyran-2,5-Dione, 3-Substituted
Isocoumarins, 4-Vinylquinoline Alkaloid, 6-Methoxymethylmorphinol,
6S-11, 13-Dihydroeremanthine, 7-Hydroxycoumarin, 7-Hydroxyfrullanolide,
a,-Glucuronidase, Abietane Diterpenes, Absolute Configurations,
a-Carbons, Acetic acid, Acetonitrile Combination, Acetyl,
Acetylharmaline, a-Chymotrypsin, Acid Lability, Aconitum falconeri,
Aconitum karakolicum, Aconitum leave, Actinidia Deliciosa, Activation,
Active, Activities, Addition, Adhatoda vasica Nees, Against,
a-Glucuronidase, a-Lactone, Alcohols, a-Hydroxyvincadifformine,
Aldehydes, Alioline, Along with, Alstozine N-Oxide, lzheimer's
disease therapy, Aminothiophene, Analysis, Analysis Based Studies,
Anamirta cocculus, Anhydrovinblastine, Anilines Carboxamides,
Anticholinergic Activity, Anticonvulsant effect, Anti-Depressant
Activities, Antidiarrhoeal, Antiferility Agents, Antileishmanial
Activity, Antileishmanial Physalins, Antimicrobial Activities,
Antimicrobial Activity, Antimicrobial Sesquiterpene Lactone,
Antimicroial Ellagic Acid Derivatives, Antisecretory, Antispasmodic,
Aplysia juliana, Apocynaceae, Aporphine-benzylisoquinoline Alkaloid,
Apparicine, Application, Arachidonic Acid, Areca catechu, Arginine,
Arjunglucoside I chloromethane 0.25-solvate monohydrate, Aromatic
Amines, Aromatic Carboxylic Scids, Aromoline, Arylsulphonyl,
Aryltetralin, Aspergillus terreus, Aspidospermidose, Bacteria,
Bannucine, Barks of Xylopia aethiopica, Barley Extracts, Based, Basis,
enzodiazepine, Benzoyl-16-acetylcycloxobuxidine, Benzylisoquinoline
Alkaloids, Berberis aristata, Berberis waziristanica, Betaine,
Betavulganrin, Bhimberine, Bicuculline-induced Epileptiform Activity,
Binary Indole Alkaloids, Bioactive chemical constituents, Bioactive
Compounds, Bioactive Flavonoids and Saponin, Bioactive Phenolic
Compounds, Bioactive Substances, Bioassay, Biocontrol Agents,
Bio-Informatics, Biologcial Activity, Biological Activities,
Biosynthesis, Bipiperidine, Biscoumarin, Blood Pressure, Bowellia
papyrifera Brideliandellensis, Broncho, Broncho-vasodilatory Activity,
Buxaceae, BuxaminolG, Buxaminone, Buxapapilinine, Buxapapillosin,
Buxaquamarine, Buxus Species, C-6 Substituents, Cadabine, Calcium
antagonistic properties, Calcium-channel blockingpotential Calculations,
Candidate, CarbazoleSynthesis, Carbohydrate, Carbohydrate
metabolicenzyme, Case, Cassia absus L. (Chaksu), Catalyzed, Catharine,
Cathovaline, CD In situ Complexation Method, Ceiba pentandra, Centaurium
pulchellum, Centaurium pulchellum Druce, Century, Cesium
Fluoride-Celite, Cesium Iodide, Chalcone, Chalinesterase Inhibitors,
Chasmaconitine 0.5-Methanol Solvate, Chemistry and Mechanism, Chemistry
of Natural Products, Chemotaxonomy, Chemotherapy, Chloride Adduct,
Cholinestease inhibitory pregnane-type steroidal alkaloids,
Cholinesterase Inhibiting Activites, Cholinesterase Inhibiting New
Steroidal Alkaloids, Cholinesterase Inhibitory, Cholinesterases,
Cinnamate Derivatives, Cinnamates, Cinnoline Derivative, Circular
Dichroism, Cleavages, Clerodendron inerme, Climacoptera obtusifolia,
Coagulin-H: Human IL-2 Novel Natural Inhibitor, Cohirsine, Colchicine
Alkaloids, Colocynthis vulgaris, Combinational Library, Commiphora
mukul, Competitive Inhibitors, Complex, Complexes, Computer Guided
Planned Synthesis, Concurrent Inhibiton, Conformation, Conformationally
Constrained Peptide Metal Complexes, Conformations, Consolida
hohenackeri, Containing, Control, Convenient, Conversion, Coronaridine,
Cortisol, Cottonogenic, Creatinine, Crude Extracts, Cs/BF3. Et2O System,
CsF-Celite/alkyl halides/CH3CN combination, Cucurbitacin
Q-1,Cucurbitacins, Cucurbitane Glycosides, Cultured Hippocampal Neurons,
Cussonia bancoensis, Cyclic, Cycloartane, Cyclobuxoviricine,
Cyclohexanone, Cyclohexanoneoxalyl, Cyclomicrobuxine monohydrate,
Cymbopogon citrates, Cyteine Based Novel Noncompetitive Inhibitors of
Urease(s), Cytotoxic Natural Products, Cytotoxicity, Danazol,
Degradative, Dehassia kurzii, Dehydroepiandrosterone, Delphinium
carduchorum, Demulsification, Deoxyvinblastine, Desmethylpecyline,
Desorption, Detoxification, Dicarboxylic Acid, Dicoumarols, Dihydro
catharanthine, Dihydrocorynantheol, Dimensional, Dimensional Nuclear
Magnetic Resonance Spectroscopy, Discaria febrifuga, Dimeric
Hydrogen-Bonded Supramolecular Complex, Dimeric Podophyllotoxin-Type
Lignan, Diploclisia glaucescens, Discoveries, Distinctive Inhibition
Susceptibility, Distribution, Diterpene Alkaloids, Diterpenoid Lactone,
Ditopic Receptor, Docking Studies, Drug, Drug Discovery, Dual Inhibitor,
Duranta repens, Dynamic, E rvatamia coronaria, E.O. Ajaiyeoba, Easy,
Eatty Ester, Effects, Efficacy, Efficient Solvent Evaporating System,
Elixirs of Love, Emodinol,Enamine Reactions, Enantiomers, Endoperoxide
Synthase, Enzyme inhibition studies, Enzyme Inhibitory Activites, Enzyme
Inhibitory Effects, Enzymes, Enzymes Inhibition Activity,
Esterase,Examples, Exciting, Exotic Withanolides, Expedient
Esterification, Extracts, Extracts of Barley, Facile Route, Factors,
Fast atom Bombardment Mass Spectrometry, Fatty Ester, Favouring,
Fermentation, Fern Adiantum incisum, Ferula mongolica, Fight Against
Cancer, First, First Microwave-Assisted Synthesis, Five, Five New
Withanolides, Flowers, Focused Library of Oxadiazoles, Four New
Flavones, Fraction, Fragmentation, Fructo-oligosaccharides, Fruit
Extract, FS-1 isolated, Fumarizine, Fungal Metabolites of
(E)-Guggulsterone, Fungus Rhizopus stolonifer, Furanoid
Bisnorditerpenoid, Furanoid Diterpenoid, Fusarium lini, Gambirtannine,
Gelidiella acerosa, Gelomuilide, Generation, Genus Buxus, Glycolipid,
Glycopeptides, Glucose Derivatives, Gossypium herbaceum, Griffithine,
Guanidino Function of Arginine, Haloxylon griffithii, Harepermine,
Harmaline (4,9-dihydro-7-methoxy-1- methyl-3H-pyrido-[3,4-b] indole),
Harmaline (4-9-dihydro-7-methoxy-1-methyl- 3Hpyrido-[3,4-b] indole),
Harmidine, Harmine, Hederagenin, Heterocycle, Hexacyanoferrate, Highly
Selective Indination of Alcohols, Highly Versatile Iodination Method,
Hippocampal Pyramidal Neurons, Human Neutrophils, Human Platelet
Aggregation, Human sperm motility, Hunteria lkaloids, Hyderabadin,
Hydrazides, Hydroxy, Hydroxylated, Hydroxylation, Hydroxyprogesterones,
Hypolipaemic E- Guggulsterone, Identity, Imidazolone, Imines,
Immunostimulant Sesquiterpene Glycoside, Imperatives for the Promotion
of Science and Technology in Pakistan, Imperatorin, Imperialine
Derivatives, Improved, Improved Method, Improved synthesis of sildenafil
(Viagra) analogs, In vitro Inhibition, In Vitro Leishmanicidal Activity,
Incorporation of 2-Amino-2-Deoxy-D-Glucose, Indacontine 0.5-Acetone
Solvate, Indole-4-ium, Indolic Imino, Indoline Alkaloid, Induced
Platelet Aggregation, Influencing, Inhibit, Inhibitory Effects,
Inhibitory Potential, Inula viscose, Iridoid, Iris Germanica Rhizomes,
Iris soforana, Irradiation, Isobenzofuran-1(3H)-ones Phthalides),
Isoflavones Irilin B, Isoflavonoids, Isolongifolen-4-one, Isomeric
Derivatives, Iso-N-Formyl-5-en-honemorphine, Isoquino [1-2-b]
quinazoline derivative, Isoquinoline Alkaloid, Isotamarixen,
Isovallesiachotamine, Jamtine N-Oxide, Jolyna laminarioides,
Juliflorine,Karachicine, Karachine, Lahoricine, Laurencia pinnatifida,
Leading, Leaves of Buxus hildebrandtii, Leaves of Erthoxylum moonii,
Leaves of Ervatamia coronaria, Leaves of Ferula oopoda, Leaves of
Murraya paniculata, Leaves of Podophyllum hexandrum, Lectones,
Leurosine, Leurosinone, Levonorgestrel, Lignans, Linear etabolite,
Linkage, Linked Scan Measurements, Linn, Lipid Profile, Lipoxygenase,
Lipoxygenase Activity, Lipoxygenase Enzyme, Logical Approach, Loranthol,
Lowering Action of Active Principle, Macroxine, Mahanine, Malabarolide,
Malarial Glycoproteins, Marine Zoanthid, Markownikov, Mass Spectral
Fragmentation, Mass Spectroscopic Studies, Mass Spectroscopic Study,
Medicinal Lichen, Mehranine, Mesterolone, Metabolism, Metabolites, Metal
Ion-Catalyzed Reduction, Metal Salts, Metal-Ion, Methanone monohydrate
737. 18. (5R, 6S, 8S, 9R, 14R, 15R, 17R, 18S, 21S, 24R, 26S,
27R)-Chloro-16, 24-cyclo-13,
14-Secoergosta-2-ene-18,26-dioicacid-14:17,14:27-diepoxy-6,13, 20,
22-tetrahydroxy-1, 15-dioxo-a-lactone a-lactone methanol solvate
monohydrate, Methoxycarbonyldihydrocleavamines, Methyl
[2,4,5--trihydroxy-6-(hydroxymethyl)-perhydropyran-3-yl]carbamate,
Methyl Ether Analogues of Sildenafil (Viagra) Possessing,
Methylacrylate, Microbial Hydroxylation, Microbial Oxidation,
Microbiological Hydroxylation, Microwave, Microwave-Assisted Synthesis,
Mimusops elengi, Mitragyna stipulosa, Mnonuclear oxovandadium (IV)
complexes, Modification, Modified, Mongolian Medicinal Plant,
Monoterpenes, Murraya paniculata, N, N'Diphenylsuccinamide,
Nahagenin,N-Alkylation, Na-Methylsecodine, N-Arylated, Natural
cholinesterase, Natural Compounds, Natural Inhibitors, Naturally
Occurring Spatozoate, Nb-Demethylalstophylline oxindole,
N-Benzoyl-30-acetoxycycloxobuxidine-F, N-Benzylsecodine,
Nb-Methylstrictamine, Neighbouring Group Participation, Nematicidal
Activity, New Antibacterial Steroidal Alkaloids, New Anticholinergic
Steroidal Alkaloid, New Antifungal Steroidal Lactones, New Approaches,
New Arylnaphthalene Lignans Glucosides, New b-Adrenoceptor Agonist, New
Benzylisoquinoline Alkaloid, New Binary Indole Alkaloid, New Biscoumarin
Derivatives, New Bisindole Alkaloids, New Class of Acid Phosphatase
Inhibitors, New Class of Cholinesterase Inhibitors, New Class of human
recombinant nucleotide pyrophosphatase phosphodiesterase-1 inhibitors,
New Class of natural cholinesterase inhibitors, New Class of
Sesterterpene, New Class of Steroidal Alkaloids, New class of Urease
inhibitors, New Coumarin, New Crystal-Engineering Motif, New Crystalline
Cevane Alkaloid, New Cyclopeptide Alkaloids, New Diepoxy-ent-kauranoid
Regosinin, New Dimeric Indoline Alkaloid, New Dinitro Derivatives, New
Diterpene Isopimara-7,15-Dien-19-OIC Acid, New Diterpenoids, New
Eudesmane Type Sesquiterpene, New Eudesmanolides, New Fungal Metabolites
of Sclareol, New Furanoid Diterpenoidal Constituents, New Glycosides,
New Indazole Alkaloid, New Isatin Derivatives, New Life to Computer
Sciences, New Mavacurine Type Alkaloid, New Non-nitrogenous
Triterpenoids, New Natural Dibenzocycloheptylamine Alkaloids, New
Norditerpenoid, New Pharmacophores, New Piperidine Alkaloid,New
Pseudoindoxyl Alkaloid, New Sesquiterpene Lactone, New Steroidal
Lactones, New Tetrahydrofuranoid Steroidal Alkaloids, New Triterpene,
N-Formylanonaine, N-Glycosidic, N-Formylcyclomicrobuxeine,
N-Imidotryptamines, Nitric Oxide, Nitrogen Heterocycles, Nitrogenus
Compounds, N-Methyltiliamosine, NMR, Norditerpene, Norethisterone,
Nortropane Alkaloids, Nucleophilic, O-Acetyljervin, Oranthus grewinkii,
Organosulfur Compounds, Organtin, Origin, Oxazolone, Oxidative,
Oxidative Fragmentation, Oxyberberine, Pakistan Encyclopaedia Planta
Medica, Papaverine Derivative, Papilicine, Papillamidine, Papraine,
Parasitemia, Peganum harmala, Pentacyclic System Isomeric,
Pentylenetetrazole, Peptide Alkaloids, Persicanidine B, Pharmacological
Evaluation, Pharmacological Screening, Phenolic glycosides, Phenolics,
Phenyl Polypropanoids, Phospholipase D Activity, Photochemical
Cyclization, Photocyclization, Photolysis, Phyllanthus fraternus,
Physalin H, Physalis minima, Phytochemical Diversity, Podophyllum emodi,
Phytopathogens, Phytotherapy, Phytotoxic Defects, Phytotoxic Effects,
Picralima Alkaloids, Picralstonine, Pinatol, Pinnatazane, Piperidines,
Plant Pathogenic Fungus Botrytis cinerea, Plant Ureases, Plants and
Aids, Plasmodium falciparum, Platelet Activating Factor, Polymeric Over,
Possessing, Possible Catabolic Route, Potassium,Potent
Immunosuppressant, Potent natural peripheral anionic-site-binding
inhibitor, Potential Source, Prednisone, Pregnenolone Derivatives,
Prevost Reaction, Principles and Guidelines, Problems, Production,
Progress, Prolyl Endopeptidase, Promising New Free-Radical Scavengers,
Prostaglandin, Protocol, Pseudaconitine, Pseudobenzylisoquinoline
Alkaloid, Pseudomonas aeruginosa, p-Toluenesulfonic Acid, Pulegone, Pure
Constituents, Pyrazoline Derivative, Quettamine--type Alkaloids,
Quinolizidine Alkaloid, Quinolizine Alkaloids, Radical- Scavenging
Screening,Rapamycin, Rapid Metal Mediated Method of Isolation, Rapid
Procedure, Rat Hippocampal Pyramidal Neurons, Rat Liver, Rats Fed on
High-fat diet, Reactions of Imines, Recent Discoveries, Reduction
Indolic Imides, Reinvestigation,Relationships, Remarkable, Research,
Reserpine Analogues, Reserpine znalogues, Respiratory Burst, Rhazicine,
Rhazidigenine--N-oxide, Rhazimanine, Rhazizine, Ritchiea capparoides
var. longiedicellata, Rodents, Root Rot Infection in Cotton, Rosicine,
Ruta montana, Saifine-N-methylleuconolam, Salsola foetida,
Salutaridinemethine, Salvia napifolia, Sapatozoate, Sarcococca
zeylanica, Sarsasapogenin, Scareolide, Scholaricine, Scientific ducation
in Muslim Countries, Sclareolide, Secokara Conitine, Sequiterpene
Lactone Achilin, Sequiterpenes, Sesquiterpenes, Several, Showing,
Significance, Simulation Studies, Six, Solation, Solid, Snake Venom
Phosphodiesterase, Soil, Solid phase, Solving, Sophazrine, Sophora
alopecuroides, Spasmolytic Potential, Specific otations, Spectral Data,
Spectral Generalizations, Spectroscopic Studies, Sri Lankan marine red
alga, Stachydrine, StachydrineL, Stapfinine, Stems and Roots of
Caesalpinia crista, Stereochemical Aspects, Stereoselectivity,
Steroidal, Steroidal Alkaloids, III, Steroidal Glycoside, Steroids,
Stimulating, Stockerine, Stockeyia indica, Stricanol, Strictamine,
Strictine, Structures, Subcellular, Substituted, Successful,
Succinylanthranilic Acid Ester, Suggested, Sulfono, Support,
Supramolecular network, Sustained Repetitive Firing, Swertia cordata,
ynthesized, Talatisamine, Tamarix hispida, Tamarix ramosissima,
Taraxerol, Tautomerism, Tautomerism-Nucleophilic, Taxane Diterpenes,
Taxilamine, Taxus baccata, Techniques, Terminalin A, Terpinolene,
Tertiary Aromatic Amides, Testerolone, Testosterone, Tetrafluoroborate,
Tetrahydroalstonine, Tetrahydrofuranoid, The Nuts and Bolts, The Role of
Natural Products in Modern Medicine, Theory of memory, Thiadiazoles,
Three New Steroidal Amines, Three Tyrosinase Inhibitors, Three
Withanolides, Thrombin inhibitory Constituents, Thrombin nhibitory
Diterpenoids, Through, Tiliaresine, Timber of Neonauclea zeylanica, Time
for 'enlightened moderation, Tocolytic Activities, Trachyspermum
ammi (L.) Sprague, Traditional Medicine, Transformations Xenobiotic,
Trends in ethnopharmacology, Trianilinophosphine oxide, Triazoles,
Trichothecium roseum, Triterpenoid Saponins, Triterpnoidal Alkaloids,
Trosinase Inhibition Studies, Turkish, Two--Dimensional NMR
Spectroscopy, Two Isofavones and Bioactivity Spectrum, Two New Aurones,
Two New Cinnamic Acid Esters, Two New Ergostane-type Steroidal Lactones,
Two New Isoflavanoids, Two New Leucosesterterpenes, Two New Quinones,
Two New Rearranged Taxoids, Two New Triterpene Lactones, Two new
Triterpenes, Two Saponins, Tyrosinaseinhibition activities, Unique,
Unusual, Ursolic Acid, Usnea longissima, V--A One-Step Synthesis,
Variably Substituted Chalcones, Variably Substituted
Pyrazolo[4,3-d]Pyrimidin-7-ones, Varninasterol, Vasodilatory, Vinca
Alkaloid, Vinca major, Vincadine, Vindoline, Vindolinine, Viral
Diseases, Viruses, Voaphylline, Weak aromatic acids, Withania species,
Wonderful, Xanthones, Zinc/Ethano, Zizyphus lotus, Zoanthaminone.
Appendix A
Table-6 Collaborator Dynamics (Comprehensive)
Sr. Authors NP [NP.sub. [NP.sub.
No. syn] isol]
1 Atta-ur-Rahman 90 9 428
2 M. I. Chaudhary 57 252
3 K. M. Khan 5 12
4 B. Sener 6 35
5 S. Anjum 14 20
6 S. Pervin 1 18
7 F. Shaheen 27
8 Habib-ur-Rahman 1 18
9 A. Farooq 4 18
10 M. Parvez 2 17
11 V. U. Ahmad 2 6
12 S. Ahmed 1 17
13 S. Turkoz 1 21
14 Hoong-Kun Fun 10 10
15 S. Malik 19
16 A. Dar 1 4
17 M. Bashir 16
18 A. Khalid 3 13
19 S. G. Musharraf 1 17
20 K. Zaman 1 11
21 M. Nisa 15
22 A. Pervin 12
23 S. Hayat 7
24 S. A. Nawaz 14
25 A. Basha
26 A. Muzaffar 15
27 W. Voelter 10
28 I. Ali 14
29 M. R. Khan 4 10
30 S. Khanum 14
31 K.T.D. De. Selva 14
32 A. Ata 2 10
33 G. M. Maharvi 1 4
34 K. A. Alvi 12
35 R. A. Ali 1 11
36 J. Clardy 11
37 N. Sultana 2 6
38 M. M. Qureshi 10
39 S. S. Ali 10
40 Zaheer-ul-Haq 2 6
41 Zia-Ullah 2
42 S. Jalil 1 8
43 M. Ghazala1 1
44 A. A. Ansari 9
45 Habib Nasir 10
46 Z. Shah 10
47 N. Fatima 2 7
48 A. H. Gilani 2 6
49 M. Shamma 10
50 T. Fatima 9
51 D. Ahmad 1 9
52 F. Nighat 10
53 S. S. Sabri 10
54 M. Abu Zarga 10
55 S. Ali 5 4
56 D. Shahwar 2 8
57 F. Akhtar 8
58 A. Abbas Khan 10
59 N. Waheed
60 S. Firdous 4
61 Y. Ahmad 5
62 M. Alam 9
63 M. S. Shekhani 1 6
64 S. Naz 3 6
65 S. A. Jamal 8
66 A. Ahmad 2 4
67 M. T. H. Khan 5
68 K. P. Devkota 1 8
69 P. W. Le Quesne 3 4
70 K. Fatima 7
71 M. Sultana 1
72 G. A. Miana 1 4
73 N. Daulatabadi 6
74 Z. Iqbal 7
75 S. Zareen 5
76 Z. Perween 1 7
77 A. Nasreen 1 5
78 T. Makhmoor 1 6
79 A. Yasin 8
80 M. A. Lodhi 1 3
81 A. J. Freyer 7
82 F. N. Ngounou 6
83 R. A. Siddiqui 2 2
84 S. Qureshi 7
85 Z. Amtul 1 5
86 M. Shabbir 7
87 M. Yaqoob 7
88 W. Gul 2 3
89 A. M. Khan 5
90 N. Nahar 7
91 I. Baig 7
92 E. Bayer 2
93 S. Nasim 1 5
94 Z. A. Siddiqui 4
95 R. Ranjit 7
96 J. Harley Mason
97 S. Farhi 6
98 M. A. Khan 1 4
99 W. S. J. Silva 6
100 S. A. Abbas 6
101 A. Nelofar 5
102 E. Asif 6
103 B. L. Sondengam 6
104 M. Feroz 5
105 K. H. C. Baser 1 5
106 M. Yousuf 1 4
107 Shahida Shujaat 4
108 A. Malik 5
109 R. J. DeLorenzo 6
110 S. Sombati 6
111 Mohsin Raza 6
112 A. Suria 6
113 I. A. Jahan 6
114 Y. Tsuda 1 5
115 Zafar S. Saify 1 1
116 A. A. Rahman 2 3
117 M. N. Sultankhodzhaev 1 1
118 S. Yousaf 1 5
119 M. A. Mesaik 1 2
120 M. N. Ghayur 2 3
121 T.M. Shrestha 6
122 L. Kenne 4
123 J. Fatima 5
124 N. M. Hasan 3
125 H. Ahmad 1 3
126 D. Lontsi 5
127 E. Dagne 2 3
128 T. H. Al-Tel 5
129 F. Noor-e-Ain 1 4
130 M. Ashraf 1 4
131 I. Orhan 4
132 M. N. Akhtar 1 4
133 S. Sultan 5
134 Atia-tul-Vakhab 2
135 M. Ahmad 4
136 N. Hasan 4
137 S. Hasan 3
138 Y. Badar 4
139 A. K. Ray 3
140 B. Mukherjee 3
141 G. Ahmad 4
142 S. K. Mitra 3
143 S. A. Saeed 4
144 G. Mukhopadhyay 3
145 M. K. Bhatti 4
146 M. Shameel 4
147 U. L. B. Jayasinghe 4
148 Khalid Aftab 2
149 N. Ahmad 4
150 O. Purev 4
151 A. Ulubelen 4
152 S. Begum 1
153 F. Asif 4
154 S. A. M. Ayatollahi 3
155 F. Demirci 1 2
156 Z. A. Abilov 1 3
157 M. Mosihuzzaman 4
158 M. Z. Khan
159 Azizuddin 4
160 S. A. A. Shah 4
161 F. Feroz 4
162 S. Hussain 3
163 S. T. A. Shah 2
164 F. Zehra 2
165 N. Perveen 2
166 G. Blasko 3
167 I. Hassan 1
168 T. Zamir 3
169 H. M. Said 1
170 K. P. Guha 2
171 D. S. Rycroft 3
172 P.M. Shah 3
173 Y. Al Abed 3
174 M. A. Maqbool 2 1
175 M. Abid 2 1
176 M. Z. Iqbal 3
177 U. Ghani 1 1
178 S. Anwar 1
179 M. Nadeem 3
180 L. M. Tillekeratne 2
181 A. Naz 3
182 K. F. Khattak 3
183 S. Jahan 1 2
184 Purev O. Ndocnii 3
185 M. Nur-e-Alam 3
186 N. Alam 3
187 S. K. Kalauni 2
188 V. B. Omurkamzinova 3
189 S. Tahara 2
190 F. Noor
191 S. Rahat
192 Mudassir Asrar 1 2
193 S. Shahnaz. 3
194 F. Ayanoglu 2
195 S. Channa 1 2
196 S. Murad
197 C. T. Supuran
198 H. Y. Gondal 3
199 M. Rani
200 S. Iqbal 1
201 Allan B. Reitz
202 Cheryl P. Kordik
203 S. Khan 3
204 Z. Ismail
205 A. Sami 3
206 M. Atif 3
207 S. Nahar Khan 1
208 B. Tashkhodzhaev 1
209 C. Karalai 2 1
210 K. K. Turgunov 1
211 S. Chantrapromma 2 1
212 J. A. Beisler
213 M. Hafeez 2
214 N. Munugesan 2
215 S. A. Drexler 2
216 A. N. Mistry 2
217 S. Kaleem 2
218 K. Albert 2
219 M. Asif 2
220 K. Jahan 2
221 I. H. Qureshi
222 T. Begum
223 T. Rasheed 2
224 S. Wasti 2
225 M. Shaiq Ali 1
226 I. I. Vohra 2
227 S. Juma Karimini 2
228 T. Wehler 1
229 K. Wurst 2
230 P. Hutter 2
231 W. Hiller 2
232 S. Balasubrama-niam 2
233 R. Zaidi 1
234 D.Shehnaz 2
235 A. Yasmin 2
236 M.Y. Khan
237 G. Topc 2
238 M. Hasan 1
239 H. Echner 1
240 A. Ghaffar 2
241 S. Shamim 2
242 S. N. Ali 2
243 A. Sultana 2
244 G. Odontuya 2
245 M. S. Ajaz 1
246 K. Usman Ghani
247 A. Jabbar 2
248 S. Z. Sultani 2
249 I. Naeem 2
250 N. Khan 2
251 S. Khatoon 1
252 D. C. Hoessli 1
253 A. Majeed 2
254 M. Iqbal 1 1
255 K. D. Hemalal 2
256 A. H. Mericli 2
257 F. Mericli 2
258 G. Toker 2
259 H. Ozcelik 2
260 K. Parvez 1
261 A. S. Mynzhasarovich
262 G. Purevsuran 2
263 M. N. Alam 2
264 T. Badarchiin 2
265 E. Anis 2
266 G. Mustafa 2
267 K. A. Tabylovich
268 N. Afza 1
269 Pir Muhammad Khan 2
270 H. Bibi 1
271 M. B. Gewali 2
272 M. D. Manandhar 2
273 I. Anis 2
274 N. Sultanova 1 1
275 B. Tuya 2
276 L. A. Tapondjou 2
277 Z. Ahmed 1
278 R. B. Tareen 2
279 N. T. Khan 1
280 N. Riaz 2
281 S. M. Haider
282 Zahid H. Chohan
283 S. Nawaz 2
284 M. K. Azim 1
285 N. Ambreen 2
286 S. Naheed 1
287 T. H. Khan 2
288 Afshan Begum 2
289 M. U. Anwar 1
290 N. Butt 1 1
291 N. R. Abdullah
292 S. Goswami 2
293 Samreen 2
294 Shafique-ur-Rehman 2
295 B. Coldman 1
296 B. Springer (ed.) 1
297 M. Zeeshan 2
298 W. Kausar 1
299 E. Foresti Serantoni
300 L. Riva de Sanseverino
301 T. Burney
302 N. H. Khan
303 B. A. Solheim
304 J. L. Occolowitz
305 R. L. Garnic
306 D. Smith
307 A. Urzaua 1
308 T. Z. Ismail 1
309 G. Sariyar 1
310 He Cun-Heng 1
311 A. Q. Khan 1
312 Ademir F. Morel 1
313 Chitra K. Ratnayake 1
314 H. Guinaudeau 1
315 L. S. R. Arambewala 1
316 M. D. Colton 1
317 A. L. Gunatilaka 1
318 C. B. Gamlath 1
319 F. Amjad 1
320 G. Crank 1
321 H. W. M. W. Herath 1
322 Helen S.M. Lu 1
323 I. Haq 1
324 K. M. I. Navaratne 1
325 L. B. De Silva 1
326 L. Paskanyi 1
327 S. Bano 1
328 S. Salam 1
329 A. Panthong 1
330 A. Z. Haq 1
331 D. Kanjanapothi 1
332 D. Shaikh 1
333 K. Bhatti 1
334 T. Taesofikul 1
335 A. Yensew 1
336 R. Ali 1
337 S. U. Kazmi 1
338 A. Kazmi
339 B. H. Shah
340 F. C. Nachnai
341 M. U. Memon
342 M. U. Valhari
343 N. Molla
344 R. R. Naqvi
345 T. Parveen 1
346 T. Sultana 1
347 Z. H. Zaidi
348 A. Badshah
349 A. Jamal 1
350 F. Mahmood 1
351 G. P. Wannigama 1
352 M. Danish
353 M. Mazhar
354 Nazar-ul-Islam
355 R. U. Simjee 1
356 G. Snatzke 1
357 T. Hussain 1
358 A. Zaman
359 C. Schroder 1
360 E. Ehtesham ul Hawue 1
361 I. Mir 1
362 K. A. Aziz 1 1
363 M. I. Khan
364 Mujeeb-ur-Rahman 1
365 Rafiuddin
366 Z. S. Siddiqui
367 M. H. Kazmi 1
368 A. Al Aboudi 1
369 B. S. Siddiqui
370 C. Muni 1
371 Chao-Zhou Ni 1
372 G. Davaa Sambuu 1
373 Ghiasuddin
374 H. Oyun 1
375 M. I. Zaidi 1
376 M. K. Kazmi 1
377 M. Kartal 1
378 M. M. Ahmad 1
379 N. M. Tirmzi 1
380 Omm-e-Hany 1
381 R. Siddiqui 1
382 S. H. Khan
383 S. Kurucu 1
384 S. Sadiq Hasan 1
385 T. L. Maksimovna 1
386 U. Sonmez 1
387 R. A. O'Neill
388 S. I. Ahmad
389 T. Sarfaraz
390 A. A. Davidson 1
391 A. H. Khan1 1
392 A. R. Siddiqui 1
393 A. S. Ijaz 1
394 G. Rahman 1
395 Nasir-ud-Din 1
396 R. Ahmad 1
397 R. Swaleh 1
398 S. Ehteshamul Haque 1
399 S. Saied 1
400 A. Hoff 1
401 A. Rauf 1
402 D. Hohnholz 1
403 E.O. Ajaiyeoba 1
404 F. Jens 1
405 H. Becker 1
406 H. D. Ratnayake 1
407 H. Zapp 1
408 J. Baumgold 1
409 N. Sattar 1
410 E. Dogru 1
411 H. Zhang
412 K. Harvey 1
413 K. Varvey 1
414 M. Shabbir Yousaf 1
415 R. Thurmer
416 W. Thomson 1
417 Y. Wang
418 A. G. Abdulkakhimovna
419 A. L. Meli1 1
420 A. Weerasooriya 1
421 B. Demirci
422 B. M. M. Kumarihamy 1
423 D.A. Dmitrievich
424 Dris Touati 1
425 F. Toker 1
426 Hafiz Rub Nawaz 1
427 J. F. Ayafor 1
428 K.B. Baurzhanovich
429 M. Bunderya 1
430 N.Jahan 1
431 S. Y. Melsovich
432 T.K. Muboryakovich
433 Z. Oyun 1
434 A. S. Amarasekare
435 G. A. Premakumara
436 K. K. S. Ng 1
437 M. N. G. James 1
438 N. Ullah 1
439 W. D. Ratnasooriya
440 W. Schumann
441 A. Kursheed
442 A. Qazi
443 E. M. Hamed 1
444 H. Latif 1
445 K. H.C. Basaric 1
446 Klaus-Peter Zeller 1
447 M. A. Khanfar 1
448 M. Ovais
449 N. A. Sultanov 1
450 A. Arfan
451 Aziz ur Rahman 1
452 D. Abdul Rahman 1
453 E. Shaheen 1
454 F. R. V. Heerden 1
455 Hee-Juhn Park 1
456 I. Erdogan 1
457 Kyung TaeLee 1
458 M. A. Anwar
459 M. A. Zaidi 1
460 M. Mizuno 1
461 M. Ozguven
462 M. Saleem
463 R. B. Bagdatovna
464 S. M. Hai
465 Y. Mimaki 1
466 Y. Sashida 1
467 Z. Sultani 1
468 A. Ajaz 1
469 A. Ejaz 1
470 A. Iqbal
471 A. Nasim
472 A. R. Raza
473 D. Brezina
474 F. I. Ansari
475 G. Musharraf 1
476 L. Hussain
477 M. A. Abbasi 1
478 M. Arfan 1
479 M. Mahroof Tahir
480 M. Moin 1
481 M. N. Sultankhod 1
482 M. Rasheed 1
483 N. M. Akhtar
484 R. Supino 1
485 S. A. Shahzad
486 A. Hasan
487 B. M. Rode 1
488 B. T. Ngadjui 1
489 C. Pakhathirathien 1
490 C. Ponglimanont 1
491 Fadimatou 1
492 H. Naz 1
493 I. Batool 1
494 I. E. Muhammad 1
495 J. M. Alam
496 K. Chantrapromma 1
497 K. Yasmen 1
498 M. Fecker
499 M. Imran-ul-Haq 1
500 M. Sajid 1
501 M. Sher
502 N. Boonnak 1
503 N. Silvere 1
504 N. Sultankhodjaev 1
505 N. T. Diderot 1
506 R. J. Abdel Jalil
507 R. Srisuwan 1
508 S. Aijaz 1
509 S. Cheenpracha 1
510 S. Dey 1
511 S. F. Kimbu 1
512 S. G. Mascara 1
513 S. I. Awan 1
514 S. Kharim 1
515 S. R Ali 1
516 S. Umbreen
517 Simeon F. Kouam 1
518 T. Etienne 1
519 T. Yousuf
520 U. T. Teshebaeva 1
521 Z. Fabien 1
522 Z. A. Khan
523 A. A. M. Ayatollahi 1
524 A. Anwar
525 A. Hazra 1
526 A. Kulsoom 1
527 A. Nasib 1
528 B. Yeskaliyeva 1
529 C. Follmer 1
530 G. Sh. Burasheva 1
531 H. K. Gill
532 J. L. Eriksen 1
533 M. A. Agzamova
534 M. Ali
535 M. I. Isaev
536 M. Mostafa 1
537 M. Q. Fatimi 1
538 N. Kausar 1
539 R. F. Rozmahel1 1
540 R. P. Mamedova
541 S. A. Kazmi 1
542 S. D. Sokeng 1
543 S. Jana 1
544 S. K. Sadozai
545 Saifullah 1
546 M. Nasir 1
547 S. M. Khalil 1
548 Z. Ali 1
Total 312 9 2149
Percentage 9.5 .27 65.2
Sr. [NP.sub. [NP.sub. SY MC SP AC Misc. F
No. x-ray] nmr]
1 9 16 131 24 23 8 28 766
2 9 3 55 10 5 5 2 398
3 25 1 43
4 1 42
5 1 3 38
6 1 15 35
7 3 1 31
8 1 3 3 1 27
9 2 24
10 3 2 24
11 4 4 4 2 22
12 2 2 22
13 22
14 1 21
15 1 20
16 1 14 20
17 3 19
18 1 2 19
19 1 19
20 2 2 1 17
21 1 16
22 2 2 16
23 9 16
24 2 16
25 2 12 1 15
26 15
27 5 15
28 1 15
29 1 15
30 14
31 14
32 1 1 14
33 1 8 14
34 1 13
35 1 13
36 1 12
37 4 12
38 2 12
39 2 12
40 1 2 1 12
41 10 12
42 1 1 1 12
43 10 11
44 1 1 11
45 1 11
46 1 11
47 1 1 11
48 1 1 1 11
49 10
50 1 10
51 10
52 10
53 10
54 10
55 1 10
56 10
57 2 10
58 10
59 9 9
60 4 1 9
61 4 9
62 9
63 1 1 9
64 9
65 1 9
66 2 1 9
67 3 1 9
68 9
69 1 8
70 1 8
71 7 8
72 2 1 8
73 1 1 8
74 1 8
75 3 8
76 8
77 2 8
78 1 8
79 8
80 4 8
81 7
82 1 7
83 2 1 7
84 7
85 1 7
86 7
87 7
88 2 7
89 1 1 7
90 7
91 7
92 5 7
93 1 7
94 3 7
95 7
96 6 6
97 6
98 1 6
99 6
100 6
101 1 6
102 6
103 6
104 1 6
105 6
106 1 6
107 1 1 6
108 1 6
109 6
110 6
111 6
112 6
113 6
114 6
115 4 6
116 1 6
117 1 1 2 6
118 6
119 2 1 6
120 1 6
121 6
122 1 5
123 5
124 1 1 5
125 1 5
126 5
127 5
128 5
129 5
130 5
131 1 5
132 5
133 5
134 1 1 1 5
135 1 5
136 4
137 1 4
138 4
139 1 4
140 1 4
141 4
142 1 4
143 4
144 1 4
145 4
146 4
147 4
148 2 4
149 4
150 4
151 4
152 3 4
153 4
154 1 4
155 1 4
156 4
157 4
158 4 4
159 4
160 4
161 4
162 1 4
163 2 4
164 1 3
165 1 3
166 3
167 2 3
168 3
169 2 3
170 1 3
171 3
172 3
173 3
174 3
175 3
176 3
177 1 3
178 2 3
179 3
180 1 3
181 3
182 3
183 3
184 3
185 3
186 3
187 1 3
188 3
189 1 3
190 3 3
191 3 3
192 3
193 3
194 1 3
195 3
196 2 1 3
197 3 3
198 3
199 3 3
200 1 1 3
201 3 3
202 1 2 3
203 3
204 2 1 3
205 3
206 3
207 2 3
208 1 1 3
209 3
210 1 1 3
211 3
212 2 2
213 2
214 2
215 2
216 2
217 2
218 2
219 2
220 2
221 2 2
222 2 2
223 2
224 2
225 1 2
226 2
227 2
228 1 2
229 2
230 2
231 2
232 2
233 1 2
234 2
235 2
236 2 2
237 2
238 1 2
239 1 2
240 2
241 2
242 2
243 2
244 2
245 1 2
246 2 2
247 2
248 2
249 2
250 2
251 1 2
252 1 2
253 2
254 2
255 2
256 2
257 2
258 2
259 2
260 1 2
261 2 2
262 2
263 2
264 2
265 2
266 2
267 2 2
268 1 2
269 2
270 1 2
271 2
272 2
273 2
274 2
275 2
276 2
277 1 2
278 2
279 1 2
280 2
281 2 2
282 2 2
283 2
284 1 2
285 2
286 1 2
287 2
288 2
289 1 2
290 2
291 1 1 2
292 2
293 2
294 2
295 1 2
296 1 2
297 2
298 1 2
299 1 1
300 1 1
301 1 1
302 1 1
303 1 1
304 1 1
305 1 1
306 1 1
307 1
308 1
309 1
310 1
311 1
312 1
313 1
314 1
315 1
316 1
317 1
318 1
319 1
320 1
321 1
322 1
323 1
324 1
325 1
326 1
327 1
328 1
329 1
330 1
331 1
332 1
333 1
334 1
335 1
336 1
337 1
338 1 1
339 1 1
340 1 1
341 1 1
342 1 1
343 1 1
344 1 1
345 1
346 1
347 1 1
348 1 1
349 1
350 1
351 1
352 1 1
353 1 1
354 1 1
355 1
356 1
357 1
358 1 1
359 1
360 1
361 1
362 1
363 1
364 1 1
365 1 1
366 1 1
367 1
368 1
369 1 1
370 1
371 1
372 1
373 1 1
374 1
375 1
376 1
377 1
378 1
379 1
380 1
381 1
382 1 1
383 1
384 1
385 1
386 1
387 1 1
388 1 1
389 1 1
390 1
391 1
392 1
393 1
394 1
395 1
396 1
397 1
398 1
399 1
400 1
401 1
402 1
403 1
404 1
405 1
406 1
407 1
408 1
409 1
410 1
411 1 1
412 1
413 1
414 1
415 1 1
416 1
417 1 1
418 1 1
419 1
420 1
421 1 1
422 1
423 1 1
424 1
425 1
426 1
427 1
428 1 1
429 1
430 1
431 1 1
432 1 1
433 1
434 1 1
435 1 1
436 1
437 1
438 1
439 1 1
440 1 1
441 1 1
442 1 1
443 1
444 1
445 1
446 1
447 1
448 1 1
449 1
450 1 1
451 1
452 1
453 1
454 1
455 1
456 1
457 1
458 1 1
459 1
460 1
461 1 1
462 1 1
463 1 1
464 1 1
465 1
466 1
467 1
468 1
469 1
470 1 1
471 1 1
472 1 1
473 1 1
474 1 1
475 1
476 1 1
477 1
478 1
479 1 1
480 1
481 1
482 1
483 1 1
484 1
485 1 1
486 1 1
487 1
488 1
489 1
490 1
491 1
492 1
493 1
494 1
495 1 1
496 1
497 1
498 1 1
499 1
500 1
501 1 1
502 1
503 1
504 1
505 1
506 1 1
507 1
508 1
509 1
510 1
511 1
512 1
513 1
514 1
515 1
516 1 1
517 1
518 1
519 1 1
520 1
521 1
522 1 1
523 1
524 1 1
525 1
526 1
527 1
528 1
529 1
530 1
531 1 1
532 1
533 1 1
534 1 1
535 1 1
536 1
537 1
538 1
539 1
540 1 1
541 1
542 1
543 1
544 1 1
545 1
546 1
547 1
548 1
48 34 527 66 59 39 54 3297
1.5 1.0 16.0 2.0 1.8 1.2 1.6
Sr. CF % C. Period
No.
1 766 23.23 1966-07
2 1164 12.07 1984-07
3 1207 1.31 1990-05
4 1249 1.27 1988-05
5 1287 1.15 1996-07
6 1322 1.06 1987-06
7 1353 0.94 1994-07
8 1380 0.82 1985-96
9 1404 0.73 1992-02
10 1428 0.73 1997-07
11 1450 0.67 1976-04
12 1472 0.67 1976-91
13 1494 0.67 1988-91
14 1515 0.64 2003-06
15 1535 0.61 1984-07
16 1555 0.61 1997-06
17 1574 0.58 1980-87
18 1593 0.58 1998-06
19 1612 0.58 2002-07
20 1629 0.52 1984-96
21 1645 0.49 1983-89
22 1661 0.49 1988-95
23 1677 0.49 1999-06
24 1693 0.49 2003-07
25 1708 0.46 1972-98
26 1723 0.46 1983-96
27 1738 0.46 1984-05
28 1753 0.46 1984-06
29 1768 0.46 1997-06
30 1782 0.43 1984-96
31 1796 0.43 1987-95
32 1810 0.43 1991-02
33 1824 0.43 2003-06
34 1837 0.39 1985-91
35 1850 0.39 1991-07
36 1862 0.36 1977-97
37 1874 0.36 1980-02
38 1886 0.36 1987-95
39 1898 0.36 1989-95
40 1910 0.36 2002-03
41 1922 0.36 2002-06
42 1934 0.36 2003-06
43 1945 0.33 1976-85
44 1956 0.33 1982-88
45 1967 0.33 1989-95
46 1978 0.33 1989-95
47 1989 0.33 1990-06
48 2000 0.33 1991-05
49 2010 0.3 1982-88
50 2020 0.3 1983-90
51 2030 0.3 1988-92
52 2040 0.3 1988-98
53 2050 0.3 1990-02
54 2060 0.3 1990-02
55 2070 0.3 1992-06
56 2080 0.3 1993-03
57 2090 0.3 1994-01
58 2100 0.3 2002-06
59 2109 0.27 1976-81
60 2118 0.27 1976-93
61 2127 0.27 1977-96
62 2136 0.27 1987-94
63 2145 0.27 1989-06
64 2154 0.27 1991-02
65 2163 0.27 1991-05
66 2172 0.27 1997-06
67 2181 0.27 2003-06
68 2190 0.27 2003-07
69 2198 0.24 1977-88
70 2206 0.24 1977-96
71 2214 0.24 1982-84
72 2222 0.24 1982-96
73 2230 0.24 1983-86
74 2238 0.24 1989-94
75 2246 0.24 1990-05
76 2254 0.24 1995-06
77 2262 0.24 1995-99
78 2270 0.24 2000-05
79 2278 0.24 2002-05
80 2286 0.24 2004-06
81 2293 0.21 1982-87
82 2300 0.21 1990-05
83 2307 0.21 1990-06
84 2314 0.21 1995-05
85 2321 0.21 1997-07
86 2328 0.21 1997-99
87 2335 0.21 1998-06
88 2342 0.21 1998-99
89 2349 0.21 1999-03
90 2356 0.21 2000-04
91 2363 0.21 2001-04
92 2370 0.21 2001-06
93 2377 0.21 2002- 05
94 2384 0.21 2003-07
95 2391 0.21 2004-07
96 2397 0.18 1966-80
97 2403 0.18 1983-89
98 2409 0.18 1984-95
99 2415 0.18 1987-90
100 2421 0.18 1987-91
101 2427 0.18 1987-91
102 2433 0.18 1988-92
103 2439 0.18 1990-05
104 2445 0.18 1991-95
105 2451 0.18 1998-02
106 2457 0.18 1998-06
107 2463 0.18 2000-04
108 2469 0.18 2000-05
109 2475 0.18 2001-01
110 2481 0.18 2001-04
111 2487 0.18 2001-04
112 2493 0.18 2001-04
113 2499 0.18 2002-04
114 2505 0.18 2002-04
115 2511 0.18 2002-04
116 2517 0.18 2003-03
117 2523 0.18 2003-05
118 2529 0.18 2004-05
119 2535 0.18 2004-06
120 2541 0.18 2004-06
121 2547 0.18 2004-07
122 2552 0.15 1982-88
123 2557 0.15 1983-86
124 2562 0.15 1989-00
125 2567 0.15 1989-89
126 2572 0.15 1990-03
127 2577 0.15 1990-95
128 2582 0.15 1991-95
129 2587 0.15 1992-97
130 2592 0.15 1994-02
131 2597 0.15 2002-04
132 2602 0.15 2002-04
133 2607 0.15 2002-04
134 2612 0.15 2003-05
135 2617 0.15 2003-07
136 2621 0.12 1983-93
137 2625 0.12 1985-00
138 2629 0.12 1986-96
139 2633 0.12 1988-91
140 2637 0.12 1988-91
141 2641 0.12 1988-91
142 2645 0.12 1988-91
143 2649 0.12 1988-95
144 2653 0.12 1989-91
145 2657 0.12 1989-95
146 2661 0.12 1991-97
147 2665 0.12 1992-00
148 2669 0.12 1993-96
149 2673 0.12 1993-97
150 2677 0.12 1995-06
151 2681 0.12 1995-99
152 2685 0.12 1997-04
153 2689 0.12 1998-00
154 2693 0.12 1998-06
155 2697 0.12 2000-02
156 2701 0.12 2001-06
157 2705 0.12 2002- 06
158 2709 0.12 2002-04
159 2713 0.12 2002-06
160 2717 0.12 2003-04
161 2721 0.12 2004-04
162 2725 0.12 2004-07
163 2729 0.12 2005-06
164 2732 0.09 1973-84
165 2735 0.09 1980-83
166 2738 0.09 1982-84
167 2741 0.09 1983-84
168 2744 0.09 1984-85
169 2747 0.09 1986-86
170 2750 0.09 1988-90
171 2753 0.09 1988-91
172 2756 0.09 1990-97
173 2759 0.09 1990-98
174 2762 0.09 1994-97
175 2765 0.09 1994-97
176 2768 0.09 1997-00
177 2771 0.09 1997-97
178 2774 0.09 1998-00
179 2777 0.09 1998-00
180 2780 0.09 1998-01
181 2783 0.09 1998-03
182 2786 0.09 1998-03
183 2789 0.09 1998-05
184 2792 0.09 2000-00
185 2795 0.09 2000-03
186 2798 0.09 2000-06
187 2801 0.09 2001-03
188 2804 0.09 2001-04
189 2807 0.09 2002-02
190 2810 0.09 2002-04
191 2813 0.09 2002-05
192 2816 0.09 2002-06
193 2819 0.09 2003-03
194 2822 0.09 2003-04
195 2825 0.09 2003-06
196 2828 0.09 2003-06
197 2831 0.09 2004-04
198 2834 0.09 2004-04
199 2837 0.09 2004-05
200 2840 0.09 2004-06
201 2843 0.09 2004-06
202 2846 0.09 2004-06
203 2849 0.09 2004-06
204 2852 0.09 2004-06
205 2855 0.09 2004-07
206 2858 0.09 2004-07
207 2861 0.09 2004-07
208 2864 0.09 2005-05
209 2867 0.09 2005-05
210 2870 0.09 2005-05
211 2873 0.09 2005-05
212 2875 0.06 1966-80
213 2877 0.06 1980-83
214 2879 0.06 1982-84
215 2881 0.06 1982-84
216 2883 0.06 1983-84
217 2885 0.06 1983-84
218 2887 0.06 1984-86
219 2889 0.06 1985-86
220 2891 0.06 1985-87
221 2893 0.06 1986-87
222 2895 0.06 1986-87
223 2897 0.06 1987-87
224 2899 0.06 1987-88
225 2901 0.06 1988-03
226 2903 0.06 1988-88
227 2905 0.06 1988-88
228 2907 0.06 1988-88
229 2909 0.06 1988-89
230 2911 0.06 1988-89
231 2913 0.06 1988-89
232 2915 0.06 1988-92
233 2917 0.06 1988-93
234 2919 0.06 1988-97
235 2921 0.06 1989-90
236 2923 0.06 1990-91
237 2925 0.06 1993-95
238 2927 0.06 1994-94
239 2929 0.06 1994-95
240 2931 0.06 1994-97
241 2933 0.06 1994-97
242 2935 0.06 1995-05
243 2937 0.06 1995-95
244 2939 0.06 1995-95
245 2941 0.06 1995-95
246 2943 0.06 1995-96
247 2945 0.06 1995-97
248 2947 0.06 1996-02
249 2949 0.06 1996-04
250 2951 0.06 1996-04
251 2953 0.06 1997-02
252 2955 0.06 1997-02
253 2957 0.06 1997-97
254 2959 0.06 1997-97
255 2961 0.06 1998-98
256 2963 0.06 1998-99
257 2965 0.06 1998-99
258 2967 0.06 1998-99
259 2969 0.06 1998-99
260 2971 0.06 1999-00
261 2973 0.06 2000-00
262 2975 0.06 2000-00
263 2977 0.06 2000-00
264 2979 0.06 2000-00
265 2981 0.06 2000-01
266 2983 0.06 2000-01
267 2985 0.06 2000-03
268 2987 0.06 2000-03
269 2989 0.06 2000-03
270 2991 0.06 2000-06
271 2993 0.06 2001-02
272 2995 0.06 2001-02
273 2997 0.06 2001-03
274 2999 0.06 2001-04
275 3001 0.06 2001-06
276 3003 0.06 2002-02
277 3005 0.06 2002-03
278 3007 0.06 2003-03
279 3009 0.06 2003-03
280 3011 0.06 2003-05
281 3013 0.06 2004-04
282 3015 0.06 2004-04
283 3017 0.06 2004-05
284 3019 0.06 2005-05
285 3021 0.06 2005-05
286 3023 0.06 2005-05
287 3025 0.06 2005-05
288 3027 0.06 2005-06
289 3029 0.06 2005-06
290 3031 0.06 2005-06
291 3033 0.06 2005-06
292 3035 0.06 2005-06
293 3037 0.06 2005-06
294 3039 0.06 2005-06
295 3041 0.06 2005-07
296 3043 0.06 2005-07
297 3045 0.06 2006-06
298 3047 0.06 2006-06
299 3048 0.03 1972-72
300 3049 0.03 1972-72
301 3050 0.03 1972-72
302 3051 0.03 1974-74
303 3052 0.03 1977-77
304 3053 0.03 1977-77
305 3054 0.03 1977-77
306 3055 0.03 1983-83
307 3056 0.03 1984-84
308 3057 0.03 1984-84
309 3058 0.03 1985-85
310 3059 0.03 1985-85
311 3060 0.03 1987-87
312 3061 0.03 1987-87
313 3062 0.03 1987-87
314 3063 0.03 1987-87
315 3064 0.03 1987-87
316 3065 0.03 1987-87
317 3066 0.03 1988-88
318 3067 0.03 1988-88
319 3068 0.03 1988-88
320 3069 0.03 1988-88
321 3070 0.03 1988-88
322 3071 0.03 1988-88
323 3072 0.03 1988-88
324 3073 0.03 1988-88
325 3074 0.03 1988-88
326 3075 0.03 1988-88
327 3076 0.03 1988-88
328 3077 0.03 1988-88
329 3078 0.03 1989-89
330 3079 0.03 1989-89
331 3080 0.03 1989-89
332 3081 0.03 1989-89
333 3082 0.03 1989-89
334 3083 0.03 1989-89
335 3084 0.03 1990-90
336 3085 0.03 1990-90
337 3086 0.03 1990-90
338 3087 0.03 1991-91
339 3088 0.03 1991-91
340 3089 0.03 1991-91
341 3090 0.03 1991-91
342 3091 0.03 1991-91
343 3092 0.03 1991-91
344 3093 0.03 1991-91
345 3094 0.03 1991-91
346 3095 0.03 1991-91
347 3096 0.03 1991-91
348 3097 0.03 1992-92
349 3098 0.03 1992-92
350 3099 0.03 1992-92
351 3100 0.03 1992-92
352 3101 0.03 1992-92
353 3102 0.03 1992-92
354 3103 0.03 1992-92
355 3104 0.03 1992-92
356 3105 0.03 1993-93
357 3106 0.03 1993-93
358 3107 0.03 1994-94
359 3108 0.03 1994-94
360 3109 0.03 1994-94
361 3110 0.03 1994-94
362 3111 0.03 1994-94
363 3112 0.03 1994-94
364 3113 0.03 1994-94
365 3114 0.03 1994-94
366 3115 0.03 1994-94
367 3116 0.03 1994-95
368 3117 0.03 1995-95
369 3118 0.03 1995-95
370 3119 0.03 1995-95
371 3120 0.03 1995-95
372 3121 0.03 1995-95
373 3122 0.03 1995-95
374 3123 0.03 1995-95
375 3124 0.03 1995-95
376 3125 0.03 1995-95
377 3126 0.03 1995-95
378 3127 0.03 1995-95
379 3128 0.03 1995-95
380 3129 0.03 1995-95
381 3130 0.03 1995-95
382 3131 0.03 1995-95
383 3132 0.03 1995-95
384 3133 0.03 1995-95
385 3134 0.03 1995-95
386 3135 0.03 1995-95
387 3136 0.03 1996-96
388 3137 0.03 1996-96
389 3138 0.03 1996-96
390 3139 0.03 1997-97
391 3140 0.03 1997-97
392 3141 0.03 1997-97
393 3142 0.03 1997-97
394 3143 0.03 1997-97
395 3144 0.03 1997-97
396 3145 0.03 1997-97
397 3146 0.03 1997-97
398 3147 0.03 1997-97
399 3148 0.03 1997-97
400 3149 0.03 1998-98
401 3150 0.03 1998-98
402 3151 0.03 1998-98
403 3152 0.03 1998-98
404 3153 0.03 1998-98
405 3154 0.03 1998-98
406 3155 0.03 1998-98
407 3156 0.03 1998-98
408 3157 0.03 1998-98
409 3158 0.03 1998-98
410 3159 0.03 1999-99
411 3160 0.03 1999-99
412 3161 0.03 1999-99
413 3162 0.03 1999-99
414 3163 0.03 1999-99
415 3164 0.03 1999-99
416 3165 0.03 1999-99
417 3166 0.03 1999-99
418 3167 0.03 2000-00
419 3168 0.03 2000-00
420 3169 0.03 2000-00
421 3170 0.03 2000-00
422 3171 0.03 2000-00
423 3172 0.03 2000-00
424 3173 0.03 2000-00
425 3174 0.03 2000-00
426 3175 0.03 2000-00
427 3176 0.03 2000-00
428 3177 0.03 2000-00
429 3178 0.03 2000-00
430 3179 0.03 2000-00
431 3180 0.03 2000-00
432 3181 0.03 2000-00
433 3182 0.03 2000-00
434 3183 0.03 2001-01
435 3184 0.03 2001-01
436 3185 0.03 2001-01
437 3186 0.03 2001-01
438 3187 0.03 2001-01
439 3188 0.03 2001-01
440 3189 0.03 2001-01
441 3190 0.03 2002-02
442 3191 0.03 2002-02
443 3192 0.03 2002-02
444 3193 0.03 2002-02
445 3194 0.03 2002-02
446 3195 0.03 2002-02
447 3196 0.03 2002-02
448 3197 0.03 2002-02
449 3198 0.03 2002-02
450 3199 0.03 2003-03
451 3200 0.03 2003-03
452 3201 0.03 2003-03
453 3202 0.03 2003-03
454 3203 0.03 2003-03
455 3204 0.03 2003-03
456 3205 0.03 2003-03
457 3206 0.03 2003-03
458 3207 0.03 2003-03
459 3208 0.03 2003-03
460 3209 0.03 2003-03
461 3210 0.03 2003-03
462 3211 0.03 2003-03
463 3212 0.03 2003-03
464 3213 0.03 2003-03
465 3214 0.03 2003-03
466 3215 0.03 2003-03
467 3216 0.03 2003-03
468 3217 0.03 2004-04
469 3218 0.03 2004-04
470 3219 0.03 2004-04
471 3220 0.03 2004-04
472 3221 0.03 2004-04
473 3222 0.03 2004-04
474 3223 0.03 2004-04
475 3224 0.03 2004-04
476 3225 0.03 2004-04
477 3226 0.03 2004-04
478 3227 0.03 2004-04
479 3228 0.03 2004-04
480 3229 0.03 2004-04
481 3230 0.03 2004-04
482 3231 0.03 2004-04
483 3232 0.03 2004-04
484 3233 0.03 2004-04
485 3234 0.03 2004-04
486 3235 0.03 2005-05
487 3236 0.03 2005-05
488 3237 0.03 2005-05
489 3238 0.03 2005-05
490 3239 0.03 2005-05
491 3240 0.03 2005-05
492 3241 0.03 2005-05
493 3242 0.03 2005-05
494 3243 0.03 2005-05
495 3244 0.03 2005-05
496 3245 0.03 2005-05
497 3246 0.03 2005-05
498 3247 0.03 2005-05
499 3248 0.03 2005-05
500 3249 0.03 2005-05
501 3250 0.03 2005-05
502 3251 0.03 2005-05
503 3252 0.03 2005-05
504 3253 0.03 2005-05
505 3254 0.03 2005-05
506 3255 0.03 2005-05
507 3256 0.03 2005-05
508 3257 0.03 2005-05
509 3258 0.03 2005-05
510 3259 0.03 2005-05
511 3260 0.03 2005-05
512 3261 0.03 2005-05
513 3262 0.03 2005-05
514 3263 0.03 2005-05
515 3264 0.03 2005-05
516 3265 0.03 2005-05
517 3266 0.03 2005-05
518 3267 0.03 2005-05
519 3268 0.03 2005-05
520 3269 0.03 2005-05
521 3270 0.03 2005-05
522 3271 0.03 2005-05
523 3272 0.03 2006-06
524 3273 0.03 2006-06
525 3274 0.03 2006-06
526 3275 0.03 2006-06
527 3276 0.03 2006-06
528 3277 0.03 2006-06
529 3278 0.03 2006-06
530 3279 0.03 2006-06
531 3280 0.03 2006-06
532 3281 0.03 2006-06
533 3282 0.03 2006-06
534 3283 0.03 2006-06
535 3284 0.03 2006-06
536 3285 0.03 2006-06
537 3286 0.03 2006-06
538 3287 0.03 2006-06
539 3288 0.03 2006-06
540 3289 0.03 2006-06
541 3290 0.03 2006-06
542 3291 0.03 2006-06
543 3292 0.03 2006-06
544 3293 0.03 2006-06
545 3294 0.03 2006-06
546 3295 0.03 2007-07
547 3296 0.03 2007-07
548 3297 0.03 2007-07
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Manzoor Ahmad Khan Anjum *
Dr. Munir Ahmad **
* Libraian, National Library of Engineering Sciences (NLES),
University of Engineering & Technology (UET), GT Road, Lahore
** Rector, National College of Busines Administration &
Economics (NCBA&E), Gulberg, Lahore
Table -1 Year-wise Productivity
S. Year Number CP % Single- %
No. of Pub author
1 196 1 1 .13 0 0
2 196 2 3 .26 0 0
3 196 1 4 .13 0 0
4 196 1 5 .13 1 0.13
5 197 3 8 .39 1 0.13
6 197 5 13 .65 3 0.39
7 197 3 16 .39 0 0
8 197 3 19 .39 0 0
9 197 4 23 .52 0 0
10 197 10 33 1.3 2 0.2
11 197 6 39 .78 3 0.39
12 197 2 41 .26 1 0.13
13 197 6 47 .78 3 0.39
14 198 7 54 .91 1 0.13
15 198 5 59 .65 2 0.2
16 198 11 70 1.4 0 0
17 198 17 87 2.2 1 0.13
18 198 31 118 4.0 3 0.39
19 198 18 13 2.3 2 0.2
20 198 27 163 3.5 3 0.39
21 198 27 19 3.5 3 0.39
22 198 39 22 5.0 5 0.65
23 198 28 25 3.6 7 0.9
24 199 23 28 3.0 4 0.52
25 199 32 312 4.1 2 0.2
26 199 25 33 3.2 4 0.52
27 199 11 348 1.4 2 0.20
28 199 22 37 2.8 3 0.39
29 199 34 40 4.4 4 0.52
30 199 14 41 1.8 1 0.13
31 199 25 44 3.2 0 0
32 199 33 47 4.3 0 0
33 199 21 49 2.7 2 0.2
34 200 20 51 2.6 3 0.39
35 200 20 53 2.6 2 0.2
36 200 37 57 4.8 4 0.52
37 200 38 612 4.9 1 0.13
38 200 41 65 5.3 1 0.13
39 200 67 72 8.7 4 0.52
40 200 34 75 4.4 3 0.39
41 2007 12 76 1.5 1 0.13
Total 766 100 83 10.8
S. Multi- % Productive
No. author A
1 1 0.13 1
2 2 0.2 2
3 1 0.13 3
4 0 0 4
5 2 0.2 6
6 2 0.2 7
7 3 0.39 8
8 3 0.39 9
9 4 0.52 10
10 8 1.05 11
11 3 0.39 12
12 1 0.13 13
13 3 0.39 14
14 6 0.78 15
15 3 0.39 16
16 11 1.44 17
17 16 2.09 18
18 28 3.6 19
19 16 2.09 20
20 24 3.13 21
21 24 3.13 22
22 34 4.44 23
23 21 2.74 24
24 19 2.48 25
25 30 3.92 26
26 21 2.74 27
27 9 1.1 28
28 19 2.48 29
29 30 3.92 30
30 13 1.7 31
31 25 3.2 32
32 33 4.3 33
33 19 2.48 34
34 17 2.22 35
35 18 2.35 36
36 33 4.3 37
37 37 4.83 38
38 40 5.22 39
39 63 8.22 40
40 31 4.05 41
41 11 1.44 42
683 89.1
* In the press or submitted for publication
Table 2--Quinquennium-wise Productivity
Q Period Number of CP % Single- CP %
Pubs. (F authored
I 1966-7 5 5 .65 2 2 0.26
II 1971-7 18 23 2.35 4 6 0.52
iii 1976-8 31 54 4.05 10 16 1.31
IV 1981-8 82 13 10.7 8 24 1.04
V 1986-9 144 28 18.8 22 46 2.87
VI 1991-9 124 40 16.19 15 61 1.96
VII 1996-0 113 51 14.75 6 67 0.78
VIII 2001-0 203 72 26.5 12 79 1.57
IX 2006-0 46 76 6.00 4 83 0.52
766 100 83 10.8
Q Multi- CP %
authored
I 3 3 0.39
II 14 17 1.83
iii 21 38 2.74
IV 74 11 9.66
V 122 23 15.9
VI 109 34 14.2
VII 107 45 13.9
VIII 191 64 24.9
IX 42 68 5.48
89.1
Q = Quinquennium
Table-3 provides detail of domain-wise authorship pattern, number of
publications and authorships in each domain of 766 publications as:
NP Natural Products
[NP.sub.syn] Natural Products--Synthesis
[NP.sub.iso] Natural Products -Isolation
[NP.sub.x-ray] Natural Products--X-Rays
[NP.sub.nmr] Natural Products--NMR
SY Synthesis
SP Spectroscopy
AC Analytical Chemistry
MC Medicinal Chemistry
Misc. Encyclopedias, Handbooks, Directories, General
topics, etc.
Table -3 Domain-wise Productivity
Domains
Papers
NP [NP.sub. [NP.sub. [NP.sub. [NP.sub. SY
syn] iso] x-ray] nmr]
1-authored 28 9 13 2 16
2-authored 18 39 1 4 39
3-authored 11 47 3 18
4-authored 7 71 1 14
5-authored 6 85 2 1 10
6-authored 13 77 4 3 11
7-authored 4 52 1 1 7
8-authored 3 19 4
9-authored 12 6
10-authored 5 6
11-authored 1 1
13-authored 1
21-authored 1
Total 90 9 423 9 14 132
Percentage 11. 1.2 55.2 1.2 1.8 17.
NP = Natural Product MC=Medicinal Chemistry
[NP.sub.syn], [NP.sub.iso], AC= Analytical Chemistry
[NP.sub.x-ray], [NP.sub.nmr]
Domains
Papers
MC SP AC Mis Tot %
1-authored 6 4 2 3 83 10.83
2-authored 5 8 1 22 13 17.89
3-authored 3 10 3 95 12.4
4-authored 6 1 10 13.05
5-authored 2 3 1 11 14.36
6-authored 2 2 11 14.62
7-authored 1 1 1 68 8.88
8-authored 26 3.39
9-authored 18 2.35
10-authored 1 12 1.57
11-authored 1 3 .39
13-authored 1 .13
21-authored 1 .13
Total 24 27 8 30 76
Percentage 3.1 3.5 1.1 3.9 100
Misc.=Reference SP=Spectroscopy
General Books SY= Synthesis
Table--4a Collaborativeships
Type of Number of % Author CF %
Productivity Contribution ships
(Y) F=X*Y
1-authored 83 10.83 83 83 2.52
2- authored 137 17.89 274 357 8.31
3-authored 95 12.4 285 642 8.65
4-authored 100 13.0 400 1042 12.13
5-authored 110 14.3 550 1592 16.68
6-authored 112 14.62 672 2264 20.38
7-authored 68 8.88 476 2740 14.44
8-authored 26 3.39 208 2948 6.31
9-authored 18 2.35 162 3110 4.91
10-authored 12 1.57 120 3230 3.64
11-authored 3 0.39 33 3263 1.00
13-authored 1 0.13 13 3276 0.39
21-authored 1 0.13 21 3297 0.64
Total 766 100 3297 100
Type of Collabora- CF %
Productivity tiveship
1-authored 0
2- authored 274 274 8.53
3-authored 285 559 8.87
4-authored 400 959 12.45
5-authored 550 1509 17.1
6-authored 672 2181 20.9
7-authored 476 2657 14.8
8-authored 208 2865 6.47
9-authored 162 3027 5.04
10-authored 120 3147 3.73
11-authored 33 3180 1.03
13-authored 13 3193 0.4
21-authored 21 3214 0.65
Total 3214 100
Table -4b Collaborativeships
Number of Number of Total
S. No. Collaborators Collaboration Collaborativeship
(X) (Y) X*Y= F
1 250 1 250
2 87 2 174
3 48 3 144
4 28 4 112
5 14 5 70
6 26 6 156
7 15 7 105
8 12 8 96
9 10 9 90
10 10 10 100
11 6 11 66
12 7 12 84
13 2 13 26
14 4 14 56
15 5 15 75
16 4 16 64
17 1 17 17
18 3 19 57
19 2 20 40
20 1 21 21
21 3 22 66
22 2 24 48
23 1 27 27
24 1 31 31
25 1 35 35
26 1 38 38
27 1 42 42
28 1 43 43
29 1 398 398
S. No. CF %
1 250 9.88
2 424 6.87
3 568 5.69
4 680 4.43
5 750 2.77
6 906 6.16
7 1011 4.15
8 1107 3.79
9 1197 3.56
10 1297 3.95
11 1363 2.61
12 1447 3.32
13 1473 1.03
14 1529 2.21
15 1604 2.96
16 1668 2.53
17 1685 0.67
18 1742 2.25
19 1782 1.58
20 1803 0.83
21 1869 2.61
22 1917 1.9
23 1944 1.07
24 1975 1.23
25 2010 1.38
26 2048 1.5
27 2090 1.66
28 2133 1.7
29 2531 15.73
Table-4c Year-wise Collaborativeships
S. No. Year Collaborativeship CF %
(F)
1 196 2 2 0.08
2 196 2 4 0.08
3 196 1 5 0.04
4 196 0 5 0
5 197 2 7 0.08
6 197 3 10 0.12
7 197 6 16 0.24
8 197 5 21 0.2
9 197 7 28 0.28
10 197 16 44 0.63
11 197 9 53 0.36
12 197 2 55 0.08
13 197 5 60 0.2
14 198 11 71 0.44
15 198 3 74 0.12
16 198 27 101 1.07
17 198 30 131 1.19
18 198 66 197 2.61
19 198 38 235 1.5
20 198 47 282 1.86
21 198 66 348 2.61
22 1988 99 447 3.91
23 1989 66 513 2.61
24 1990 71 584 2.81
25 1991 119 703 4.7
26 1992 64 767 2.53
27 1993 32 799 1.2
28 1994 76 875 3.00
29 1995 110 985 4.35
30 1996 32 101 1.2
31 1997 85 110 3.3
32 1998 119 122 4.7
33 1999 71 129 2.81
34 2000 82 137 3.24
35 2001 97 147 3.83
36 2002 143 161 5.65
37 2003 185 179 7.31
38 2004 207 200 8.18
39 2005 318 232 12.5
40 2006 160 248 6.32
41 Sub 47 253 1.86
Total 253
Table -4d Quinquennium-wise Collaborativeships
Quinquennium Period Collaborativeships CF %
(F)
I 1966-70 5 5 0.2
II 1971-75 23 28 0.91
III 1976-80 43 71 1.7
IV 1981-85 164 235 6.48
V 1986-90 349 584 13.79
VI 1991-95 401 985 15.84
VII 1996-00 389 1374 15.37
VIII 2001-05 950 2324 37.53
IX 2006-07 207 2531 8.18
Table-5 Mentor's Authorship Credibility
Authorship Position Frequency (F) CF %
1st author 444 444 57.96
2nd author 74 518 9.66
3rd author 41 559 5.35
4th author 49 608 6.4
5th author 55 663 7.18
6th author 49 712 6.4
7th author 26 738 3.39
8th author 11 749 1.44
9th author 12 761 1.57
10th author 2 763 0.26
11th author 3 766 0.39
Table-7 Year-wise Detail of New & Overlapping Collaborators
S. No. Year (F) CF % (F-1)
1 1966 2 2 0.08 2
2 1967 2 4 0.08 0
3 1968 1 5 0.04 0
4 1969 0 5 0 0
5 1971 2 7 0.08 0
6 1972 3 10 0.12 2
7 1973 6 16 0.24 3
8 1974 5 21 0.2 1
9 1975 7 28 0.28 0
10 1976 16 44 0.63 5
11 1977 9 53 0.36 7
12 1978 2 55 0.08 0
13 1979 5 60 0.2 0
14 1980 11 71 0.44 4
15 1981 3 74 0.12 0
16 1982 27 101 1.07 9
17 1983 30 131 1.19 11
18 1984 66 197 2.61 11
19 1985 38 235 1.5 7
20 1986 47 282 1.86 4
21 1987 66 348 2.61 15
22 1988 99 447 3.91 35
23 1989 66 513 2.61 16
24 1990 71 584 2.81 16
25 1991 119 703 4.7 18
26 1992 64 767 2.53 12
27 1993 32 799 1.26 6
28 1994 76 875 3.00 19
29 1995 110 985 4.35 30
30 1996 32 1017 1.26 7
31 1997 85 1102 3.36 23
32 1998 119 1221 4.7 28
33 1999 71 1292 2.81 11
34 2000 82 1374 3.24 34
35 2001 97 1471 3.83 21
36 2002 143 1614 5.65 30
37 2003 185 1799 7.31 37
38 2004 207 2006 8.18 40
39 2005 318 2324 12.5i 55
40 2006 160 2484 6.32 25
41 2007 47 2531 1.86 3
2531 100 547
S. No. CF % (F-2) CF %
1 2 0.08 0 0 0
2 2 0 2 2 0.08
3 2 0 1 3 0.04
4 2 0 0 3 0
5 2 0 2 5 0.08
6 4 0.08 1 6 0.04
7 7 0.12 3 9 0.12
8 8 0.04 4 13 0.16
9 8 0 7 20 0.28
10 13 0.2 11 31 0.44
11 20 0.28 2 33 0.08
12 20 0 2 35 0.08
13 20 0 5 40 0.2
14 24 0.16 7 47 0.28
15 24 0 3 50 0.12
16 33 0.36 18 68 0.71
17 44 0.44 19 87 0.75
18 55 0.44 55 142 2.17
19 62 0.28 31 173 1.23
20 66 0.16 43 216 1.7
21 81 0.6 51 267 2.02
22 116 1.38 64 331 2.53
23 132 0.63 50 381 1.98
24 148 0.63 55 436 2.17
25 166 0.71 101 537 3.99
26 178 0.47 52 589 2.06
27 184 0.24 26 615 1.03
28 203 0.75 57 672 2.25
29 233 1.19 80 752 3.16
30 240 0.28 25 777 0.99
31 263 0.91 62 839 2.45
32 291 1.11 91 930 3.6
33 302 0.44 60 990 2.37
34 336 1.34 48 1038 1.9
35 357 0.83 76 1114 3.0
36 387 1.19 113 1227 4.47
37 424 1.46 148 1375 5.85
38 464 1.58 167 1542 6.6
39 519 2.17 263 1805 10.39
40 544 0.99 135 1940 5.33
41 547 0.12 44 1984 1.74
21.6 1984 78.44
F = Total Collaboratorships, F-1 = New collaborators, F-2 =
Overlapping collaborators
Table-8 Quinquennium-wise detail of New & Overlapping Collaborators
Q Period (F) CF % (F-1)
I 1966-7 5 5 0.2 2
II 1971-7 23 28 0.9 6
III 1976-8 43 71 1.7 16
IV 1981-8 164 235 6.5 38
V 1986-9 349 584 13.8 86
VI 1991-9 401 985 15.8 85
VI 1996-0 389 1374 15.4 103
VII 2001-0 950 2324 37.5 183
IX 2006-0 207 2531 8.2 28
2531 100
Q CF % (F-2) CF %
I 2 0.08 3 3 0.12
II 8 0.24 17 20 0.67
III 24 0.63 27 47 1.07
IV 62 1.5 126 173 4.98
V 148 3.4 263 436 10.39
VI 233 3.36 316 752 12.49
VI 336 4.1 286 1038 11.3
VII 519 7.23 767 1805 30.3
IX 547 1.11 179 1984 7.07
21.6 1984 78.39
Q=Quinquennium, F=Collaboratorships, F-1= New collaborators, F-2=
Overlapping collaborators
Table 9-Channels of communication
S. No. Channel of Communication F % CF
1 Photochemistry 93 12.14 93
2 Elsevier Science Publishers 56 7.31 149
3 J. Nat. Prod 56 7.31 205
4 Planta Medica 48 6.27 253
5 Heterocycles 35 4.57 288
6 Nat. Prod. Letters 30 3.92 318
7 Z. Naturforch 28 3.66 346
8 J. Chem. Soc. Pak 27 3.53 373
9 Acta Cryst. 21 2.74 394
10 Chem. Pharm. Bull. 19 2.48 413
11 Natural product research 17 2.22 430
12 Tetrahedron Lett 17 2.22 447
13 Fitoterapia 15 1.96 462
14 Patent Offices 15 1.96 477
15 COMSTECH 14 1.84 491
16 Bioorganic & Med. Chemistry 12 1.57 503
17 Helv. Chim. Acta 12 1.57 515
18 J. of Ethnopharmacology 12 1.57 527
19 Tetrahedron 11 1.44 538
20 Bentham Science 9 1.18 547
21 Chem & biodver 9 1.18 556
22 Elite Publishers 9 1.18 565
23 J. Chem. Soc 9 1.17 574
24 Pure & Applied Chemistry 9 1.18 583
25 B.C.C. & T. Press 7 0.91 590
26 Pak. J. Sci. Indus. Res. 7 0.91 597
27 Springer Verlag 7 0.91 604
28 Academic Press 6 0.78 610
29 J. of Enzyme Inhibition 6 0.78 616
and Me Chemistry
30 Phytotheraphy Research 6 0.78 622
31 Hamdard Foundation Press 5 0.65 627
32 Biochemical and Biophysical 4 0.52 631
Re Comm.
33 Harwood Academic 4 0.52 635
34 J. Chem. Soc. Perkin Trans. 4 0.52 639
35 Letters in Organic Chemistry 4 0.52 643
36 Nat. Prod. Rep 4 0.52 647
37 Quaid-e-Azam University 4 0.52 651
38 Shamim Printing Press 4 0.52 655
39 Chem. of Natural Compounds 3 0.39 658
40 Curr. Pharm. Design 3 0.39 661
41 J. Am. Chem. Soc. 3 0.39 664
42 Pak. J. Science 3 0.39 667
43 Phytomedicine 3 0.39 670
44 Steroids 3 0.39 673
45 Alken Inc 2 0.26 675
46 Arzneim Forsch. Drug Res. 2 0.26 677
47 Biochemica 2 0.26 679
48 Chem. of Hetrocyclic Comps. 2 0.26 681
49 Crystal Structure Comm. 2 0.26 683
50 Current Organic Chemistry 2 0.26 685
51 Experientia 2 0.26 687
52 J. Org. Chem. 2 0.26 689
53 Molecular Diversity 2 0.26 691
54 Nature 2 0.26 693
55 Organic Lettres 2 0.26 695
56 Plenum 2 0.26 697
57 Proc. Pak. Acad. Sciences 2 0.26 699
58 Synthetic Communications 2 0.26 701
59 Acta Agrobotanica 1 0.13 702
60 Arch. Pharm. Res. 1 0.13 703
61 Asian J. Androl 1 0.13 704
62 Biochem. Soc. Trans.actions 1 0.13 705
63 Biosci. Biotechnol. Biochem. 1 0.13 706
64 Blackwell Scientific 1 0.13 707
65 Bulgarian Academy of Sc. 1 0.13 708
66 Carbohydrate research 1 0.13 709
67 Chem. Nat. comp. 1 0.13 710
68 Chemistry and Industry 1 0.13 711
69 Chemistry in Britain 1 0.13 712
70 Clarendon 1 0.13 713
71 Cryst. Eng. Comm. 1 0.13 714
72 Current Medicinal Chemistry 1 0.13 715
73 Frontiers in Nat. Prod. Chem. 1 0.13 711
74 Hamdard Medicus 1 0.13 717
75 I. U. P. A. C 1 0.13 718
76 Indian J. Chem. 1 0.13 719
77 Ins. Union of Crystallography 1 0.13 720
78 J. of Science 1 0.13 721
79 J. Chem. Educ. 1 0.13 722
80 J. Chem. Res. 1 0.13 723
81 J. FASEB 1 0.13 724
82 J. Mol. Bio. 1 0.13 725
83 J. Natn. Sci. Coun. 1 0.13 726
84 J. of Inorganic Biochemistry 1 0.13 727
85 J. Pharm. Med. 1 0.13 728
86 J. Pharm. Sci. 1 0.13 729
87 J. Pract. Chem. 1 0.13 730
88 J. Science & Medicine 1 0.13 731
89 Journal of Pharm. Society 1 0.13 732
90 J. of Heterocyclic Chemitry 1 0.13 733
91 Kluwer Plenum 1 0.13 734
92 Letters in Drug Desing 1 0.13 735
& Discovery
93 Magn. Reson. Chem. 1 0.13 736
94 Molecular Immunology 1 0.13 737
95 Munksgaard, Copenhagen 1 0.13 738
96 N. Triter. Alkl. Cholines 1 0.13 739
97 Neuroscience Letters 1 0.13 740
98 New Trends in Nat Prod. 1 0.13 741
Chemistry
99 Organic Mass Spectrometry 1 0.13 742
100 Oxford University 1 0.13 743
101 Pak. J. Anal. Chem. 1 0.13 744
102 Pakistan J. of Hematology 1 0.13 745
103 Pakistan Med. Jour. 1 0.13 746
104 Print Arts 1 0.13 747
105 Proc. ISBBP Symp. 1 0.13 748
Biochem. Biophys
106 Recent Trends in Biomed. 1 0.13 749
Res. i Pakistan
107 Royal Society of Chemistry 1 0.13 750
108 Social and Natural Sciences 1 0.13 751
109 Synthesis 1 0.13 752
110 Turk. J. Chem. 1 0.13 753
111 UGC Press 1 0.13 754
112 Vanguard Books 1 0.13 755
113 Yaulor & Farncis 1 0.13 756
114 Name not mentioned 10 1.31 766
76 100
S. No. Loc % Foreig %
1 93 12.1
2 56 7.31
3 56 7.31
4 48 6.27
5 35 4.57
6 30 3.92
7 28 3.66
8 27 3.52
9 21 2.74
10 19 2.48
11 17 2.22
12 17 2.22
13 15 1.96
14 10 1.31 5 0.65
15 14 1.83
16 12 1.57
17 12 1.57
18 12 1.57
19 11 1.44
20 9 1.18
21 9 1.18
22 9 1.18
23 9 1.17
24 9 1.18
25 7 0.91
26 7 0.91
27 7 0.91
28 6 0.78
29 6 0.78
30 6 0.78
31 5 0.65
32 4 0.52
33 4 0.52
34 4 0.52
35 4 0.52
36 4 0.52
37 4 0.52
38 4 0.52
39 3 0.39
40 3 0.39
41 3 0.39
42 3 0.39
43 3 0.39
44 3 0.39
45 2 0.26
46 2 0.26
47 2 0.26
48 2 0.26
49 2 0.26
50 2 0.26
51 2 0.26
52 2 0.26
53 2 0.26
54 2 0.26
55 2 0.26
56 2 0.26
57 2 0.26
58 2 0.26
59 1 0.13
60 1 0.13
61 1 0.13
62 1 0.13
63 1 0.13
64 1 0.13
65 1 0.13
66 1 0.13
67 1 0.13
68 1 0.13
69 1 0.13
70 1 0.13
71 1 0.13
72 1 0.13
73 1 0.13
74 1 0.13
75 1 0.13
76 1 0.13
77 1 0.13
78 1 0.13
79 1 0.13
80 1 0.13
81 1 0.13
82 1 0.13
83 1 0.13
84 1 0.13
85 1 0.13
86 1 0.13
87 1 0.13
88 1 0.13
89 1 0.13
90 1 0.13
91 1 0.13
92 1 0.13
93 1 0.13
94 1 0.13
95 1 0.13
96 1 0.13
97 1 0.13
98 1 0.13
99 1 0.13
100 1 0.13
101 1 0.13
102 1 0.13
103 1 0.13
104 1 0.13
105 1 0.13
106 1 0.13
107 1 0.13
108 1 0.13
109 1 0.13
110 1 0.13
111 1 0.13
112 1 0.13
113 1 0.13
114 2 0.26 8 1.04
106 13.84 660 86.1
Table 10- Geographical Detail of Productivity
S. No. Country F CF %
1 UK 220 220 28.7
2 USA 131 351 17.1
3 Pakistan 106 457 13.84
4 Germany 91 548 11.88
5 The Netherland 89 637 11.62
6 Japan 57 694 7.41
7 Switzerland 35 729 4.57
8 Italy 13 742 1.7
9 Canada 7 749 0.91
10 Brazil 2 751 0.26
11 Ireland 2 753 0.26
12 Sri Lanka 2 755 0.26
13 Bulgaria 1 756 0.13
14 Denmark 1 757 0.13
15 Hungary 1 758 0.13
16 India 1 759 0.13
17 Indonesia 1 760 0.13
18 Kazakhstan 1 761 0.13
19 Korea 1 762 0.13
20 Nepal 1 763 0.13
21 New Zealand 1 764 0.13
22 Thailand 1 765 0.13
23 Turkey 1 766 0.13
766 100
S. No. Foreig % Loca %
1 220 28.7
2 131 17.1
3 106 13.8
4 91 11.8:
5 89 11.6
6 57 7.41
7 35 4.57
8 13 1.7
9 7 0.91
10 2 0.26
11 2 0.26
12 2 0.26
13 1 0.13
14 1 0.13
15 1 0.13
16 1 0.13
17 1 0.13
18 1 0.13
19 1 0.13
20 1 0.13
21 1 0.13
22 1 0.13
23 1 0.13
660 86.1 106 13.8.