Post on 28-Jul-2020
Are authors and journalson the same page?
J Peter Donnelly BSc PhD FRCPathEditor in Chief
Some metrics
Journal of Antimicrobial ChemotherapyThe Journal of the British Society for Antimicrobial Chemotherapy
A joint enterprise
Journal of Antimicrobial Chemotherapy
Journal
Establishedin 1975
A joint enterprise
Journal of Antimicrobial Chemotherapy
British Society of Antimicrobial Chemotherapy
Journal
OwnerEstablished
in 1975
A joint enterprise
Journal of Antimicrobial Chemotherapy
British Society of Antimicrobial Chemotherapy
Oxford University Press
Journal
Publisher OwnerEstablished
in 1975
EiCs through the years
0
1
2
3
4
5
6
0
100
200
300
400
500
600
19
75
19
76
19
77
19
78
19
79
19
80
19
81
19
82
19
83
19
84
19
85
19
86
19
87
19
88
19
89
19
90
19
91
19
92
19
93
19
94
19
95
19
96
19
97
19
98
19
99
20
00
20
01
20
02
20
03
20
04
20
05
20
06
20
07
20
08
20
09
20
10
20
11
20
12
20
13
20
14
20
15
20
16
20
17
20
18
Jo
urn
al Im
pa
ct
Fa
cto
r
Nu
mb
er
of
art
icle
s p
ub
lis
he
d
EiCs through the years
0
1
2
3
4
5
6
0
100
200
300
400
500
600
19
75
19
76
19
77
19
78
19
79
19
80
19
81
19
82
19
83
19
84
19
85
19
86
19
87
19
88
19
89
19
90
19
91
19
92
19
93
19
94
19
95
19
96
19
97
19
98
19
99
20
00
20
01
20
02
20
03
20
04
20
05
20
06
20
07
20
08
20
09
20
10
20
11
20
12
20
13
20
14
20
15
20
16
20
17
20
18
Jo
urn
al Im
pa
ct
Fa
cto
r
Nu
mb
er
of
art
icle
s p
ub
lis
he
d
EiCs through the years
0
1
2
3
4
5
6
0
100
200
300
400
500
600
19
75
19
76
19
77
19
78
19
79
19
80
19
81
19
82
19
83
19
84
19
85
19
86
19
87
19
88
19
89
19
90
19
91
19
92
19
93
19
94
19
95
19
96
19
97
19
98
19
99
20
00
20
01
20
02
20
03
20
04
20
05
20
06
20
07
20
08
20
09
20
10
20
11
20
12
20
13
20
14
20
15
20
16
20
17
20
18
Jo
urn
al Im
pa
ct
Fa
cto
r
Nu
mb
er
of
art
icle
s p
ub
lis
he
d
Pre-JIF
0,0
1,0
2,0
3,0
4,0
5,0
6,0
7,0
2005 2006 2007 2008 2009 2010 2011 2012 2013 2014 2015 2016 2017
JO
UR
NA
L I
MP
AC
T F
AC
TO
R
JAC = 5.217I
CMI = 5.394
AAC = 4.215
IJAA = 4.215
Journal impact factors
Submissions
Journal of Antimicrobial ChemotherapyThe Journal of the British Society for Antimicrobial Chemotherapy
0
200
400
600
800
1000
1200
1400
1600
1800
2000
2200
2400
1988 1990 1992 1994 1996 1998 2000 2002 2004 2006 2008 2010 2012 2014 2016 2018
Nu
mb
er
of
art
icle
s s
ub
mit
ted
Submissions
0
200
400
600
800
1000
1200
1400
1600
1800
2000
2200
2400
1988 1990 1992 1994 1996 1998 2000 2002 2004 2006 2008 2010 2012 2014 2016 2018
Nu
mb
er
of
art
icle
s s
ub
mit
ted
Submissions
~40 per week
Types of articles - 2018
Leading article1%
For debate1%
Letter to the Editor3%
Systematic Review3%
Review3%
Research letter11%
Original research
78%
Downloaded articles - 2018
0
50.000
100.000
150.000
200.000
250.000
Do
wn
load
s
HTML Full-text
JAC is global
80 countries
Origin of articles submitted - 2018
United States 11%
China 11%
United Kingdom 10%
France 8%
Spain 7%
Italy 5%
Australia 4%
India 4%
Brazil 4%
Netherlands 3%
Germany 3%
South Korea 3%
Taiwan 2%
Japan 2%
Canada 2%
Belgium 2%
Switzerland 1%
South Africa 1%
Iran 1%
Sweden 1%
Turkey 1%
Singapore 1%
Portugal 1%
Thailand 1%
Hong Kong 1%
Greece 1%
others (n= 57)10%
Origin of articles submitted - 2018
United States 11%
China 11%
United Kingdom 10%
France 8%
Spain 7%
Italy 5%
Australia 4%
India 4%
Brazil 4%
Netherlands 3%
Germany 3%
South Korea 3%
Taiwan 2%
Japan 2%
Canada 2%
Belgium 2%
Switzerland 1%
South Africa 1%
Iran 1%
Sweden 1%
Turkey 1%
Singapore 1%
Portugal 1%
Thailand 1%
Hong Kong 1%
Greece 1%
others (n= 57)10%
50% from 6 countries
Authorship
Journal of Antimicrobial ChemotherapyThe Journal of the British Society for Antimicrobial Chemotherapy
Criteria for authorship
The ICMJE recommends that authorship be based on EACH of the following 4 criteria:
http://www.icmje.org
Criteria for authorship
The ICMJE recommends that authorship be based on EACH of the following 4 criteria:
Substantial contributions to the conception or design of the work, or the acquisition, analysis, or interpretation of data for the work
http://www.icmje.org
Criteria for authorship
The ICMJE recommends that authorship be based on EACH of the following 4 criteria:
Substantial contributions to the conception or design of the work, or the acquisition, analysis, or interpretation of data for the work
Drafting the work or revising it critically for important intellectual content
http://www.icmje.org
Criteria for authorship
The ICMJE recommends that authorship be based on EACH of the following 4 criteria:
Substantial contributions to the conception or design of the work, or the acquisition, analysis, or interpretation of data for the work
Drafting the work or revising it critically for important intellectual content
Final approval of the version to be published
http://www.icmje.org
Criteria for authorship
The ICMJE recommends that authorship be based on EACH of the following 4 criteria:
Substantial contributions to the conception or design of the work, or the acquisition, analysis, or interpretation of data for the work
Drafting the work or revising it critically for important intellectual content
Final approval of the version to be published
Agreement to be accountable for all aspects of the work in ensuring that questions related to the accuracy or integrity of any part of the work are appropriately investigated and resolved.
http://www.icmje.org
Instructions for authors
Journal of Antimicrobial ChemotherapyThe Journal of the British Society for Antimicrobial Chemotherapy
JAC homepage
Author guidelines
Author guidelines
Background
The Journal of Antimicrobial Chemotherapy was founded in 1975 by the British
Society for Antimicrobial Chemotherapy (BSAC) as part of its mission to facilitate
the acquisition and dissemination of knowledge in the field of antimicrobial
chemotherapy. Proceeds from the Journal are used by the BSAC to further these
objectives. Articles are published continuously online in JAC Advance Access
and assembled into monthly printed and online issues. The Journal has an
Impact Factor of 5.217 (2017).
Author guidelines
BACKGROUND AND SCOPE OF THE JOURNAL
Aims
The Journal publishes articles that further knowledge and advance the science
and application of antimicrobial chemotherapy with antibiotics and antifungal,
antiviral and antiprotozoal agents. The Journal publishes primarily in human
medicine, and articles in veterinary medicine likely to have an impact on global
health.
Author guidelines
BACKGROUND AND SCOPE OF THE JOURNAL
Scope
The Journal particularly welcomes manuscripts on:
the practice of evidence-based medicine relating to antimicrobials (clinical
trials, systematic reviews and meta-analyses)
antimicrobial treatment (pharmacokinetics, pharmacodynamics and
prescribing practices)
the action of antimicrobial agents and the mechanisms, genetics and
epidemiology of antimicrobial resistance
antimicrobial stewardship
the genetic basis of antimicrobial resistance
Author guidelines
BACKGROUND AND SCOPE OF THE JOURNAL
Scope
In addition, the Journal is very keen to publish articles that:
offer evidence-based synthesis of knowledge and data useful for clinical
practice
analyse, reflect and comment on the current state of the art and practice
consolidate our knowledge of antimicrobial agents and their use
consider the future of antimicrobial chemotherapy
Author guidelines
BACKGROUND AND SCOPE OF THE JOURNAL
Scope
The Journal will consider publishing articles on:
new approaches to improving antimicrobial chemotherapy
new compounds provided evidence is offered of selective antimicrobial activity
and comparative cytotoxicity data
previously unreported antimicrobial activity relating to a marketed drug product
but such studies must take into account the exposure to the drug that can be
safely achieved with clinically acceptable doses
articles reporting the activity of bacteriophages
Author guidelines
BACKGROUND AND SCOPE OF THE JOURNAL
Scope
The Journal will not usually consider publishing material on:
the chemical synthesis or characterization of compounds. These are better
suited to chemistry journals.
the use and activity of biocides or disinfectants. These require specialist
methodology and are generally better suited to more specialist journals.
the process of turning antimicrobials into a medication i.e. pharmaceutics.
These are better suited to a pharmacy journal
drug stability studies
naturally occurring substances or extracts that exhibit antimicrobial activity but
for which no specific active ingredient has been chemically defined
Author guidelines
BACKGROUND AND SCOPE OF THE JOURNAL
The filtering process
The filtering process
The filtering process
aims and scope
The filtering process
aims and scope
editorial review
The filtering process
aims and scope
editorial review
peer review
The filtering process
aims and scope
editorial review
peer review
published
Fate of submissions
Journal of Antimicrobial ChemotherapyThe Journal of the British Society for Antimicrobial Chemotherapy
Fate of submissions
Immediate rejection -
outside scope12%
Immediate rejection -
appeal, merit, quality
25%
Rejection after review
39%
Acceptance24%
Fate of submissions - 2018
Immediate rejection -
outside scope12%
Immediate rejection -
appeal, merit, quality
25%
Rejection after review
39%
Acceptance24%
76% rejection
rate
Origin of articles published
United Kingdom 16%
United States 15%
France 12%
Netherlands 6%
Spain 6%
China 6%
Italy 5%
Australia 5%
Germany 4%
Belgium 3%
Canada 3%
Brazil 3%
Switzerland 2%
Sweden 1%
South Korea 1%
Taiwan 1%
South Africa 1%
India 1%
Hong Kong 1%
Others (n=25)9%
50% from 5 countries
Origin of articles published
United Kingdom 16%
United States 15%
France 12%
Netherlands 6%
Spain 6%
China 6%
Italy 5%
Australia 5%
Germany 4%
Belgium 3%
Canada 3%
Brazil 3%
Switzerland 2%
Sweden 1%
South Korea 1%
Taiwan 1%
South Africa 1%
India 1%
Hong Kong 1%
Others (n=25)9%
31% native English speakers
Editorial management
Journal of Antimicrobial ChemotherapyThe Journal of the British Society for Antimicrobial Chemotherapy
Editorial tree
Senior editors
Editorial tree
Senior editors
Editors
The manuscript
Editorial process
1
Mol ecul ar st r uct ur e of Nucl ei c Aci ds
WATSON, J. D. & CRICK, F. H. C.
Medical Research Council Unit for the Study of Molecular Structure
of Biological Systems, Cavendish Laboratory, Cambridge.
A St r uct ur e f or Deoxyr i bose Nucl ei c Aci d
We wish to suggest a structure for the salt of deoxyribose nucleic
acid (D.N.A.). This structure has novel features which are of
considerable biological interest.
A structure for nucleic acid has already been proposed by Pauling
and Corey1. They kindly made their manuscript available to us in
advance of publication. Their model consists of three intertwined
chains, with the phosphates near the fibre axis, and the bases on
the outside. In our opinion, this structure is unsatisfactory for
two reasons: (1) We believe that the material which gives the X-
ray diagrams is the salt, not the free acid. Without the acidic
hydrogen atoms it is not clear what forces would hold the
structure together, especially as the negatively charged
phosphates near the axis will repel each other. (2) Some of the
van der Waals distances appear to be too small.
Another three-chain structure has also been suggested by Fraser
(in the press). In his model the phosphates are on the outside and
the bases on the inside, linked together by hydrogen bonds. This
structure as described is rather ill-defined, and for this reason
we shall not comment on it.
We wish to put forward a radically different structure for the
salt of deoxyribose nucleic acid. This structure has two helical
chains each coiled round the same axis (see diagram). We have made
the usual chemical assumptions, namely, that each chain consists
of phosphate diester groups joining ß-D-deoxyribofuranose residues
with 3',5' linkages. The two chains (but not their bases) are
related by a dyad perpendicular to the fibre axis. Both chains
follow right- handed helices, but owing to the dyad the sequences
of the atoms in the two chains run in opposite directions. Each
chain loosely resembles Furberg's2 model No. 1; that is, the bases
are on the inside of the helix and the phosphates on the outside.
The configuration of the sugar and the atoms near it is close to
Furberg's 'standard configuration', the sugar being roughly
perpendicular to the attached base. There is a residue on each
every 3.4 A. in the z-direction. We have assumed an angle of 36° between adjacent residues in the same chain, so that the structure
repeats after 10 residues on each chain, that is, after 34 A. The
distance of a phosphorus atom from the fibre axis is 10 A. As the
phosphates are on the outside, cations have easy access to them.
The structure is an open one, and its water content is rather
Editorial process
AdminChecklist
1
Mol ecul ar st r uct ur e of Nucl ei c Aci ds
WATSON, J. D. & CRICK, F. H. C.
Medical Research Council Unit for the Study of Molecular Structure
of Biological Systems, Cavendish Laboratory, Cambridge.
A St r uct ur e f or Deoxyr i bose Nucl ei c Aci d
We wish to suggest a structure for the salt of deoxyribose nucleic
acid (D.N.A.). This structure has novel features which are of
considerable biological interest.
A structure for nucleic acid has already been proposed by Pauling
and Corey1. They kindly made their manuscript available to us in
advance of publication. Their model consists of three intertwined
chains, with the phosphates near the fibre axis, and the bases on
the outside. In our opinion, this structure is unsatisfactory for
two reasons: (1) We believe that the material which gives the X-
ray diagrams is the salt, not the free acid. Without the acidic
hydrogen atoms it is not clear what forces would hold the
structure together, especially as the negatively charged
phosphates near the axis will repel each other. (2) Some of the
van der Waals distances appear to be too small.
Another three-chain structure has also been suggested by Fraser
(in the press). In his model the phosphates are on the outside and
the bases on the inside, linked together by hydrogen bonds. This
structure as described is rather ill-defined, and for this reason
we shall not comment on it.
We wish to put forward a radically different structure for the
salt of deoxyribose nucleic acid. This structure has two helical
chains each coiled round the same axis (see diagram). We have made
the usual chemical assumptions, namely, that each chain consists
of phosphate diester groups joining ß-D-deoxyribofuranose residues
with 3',5' linkages. The two chains (but not their bases) are
related by a dyad perpendicular to the fibre axis. Both chains
follow right- handed helices, but owing to the dyad the sequences
of the atoms in the two chains run in opposite directions. Each
chain loosely resembles Furberg's2 model No. 1; that is, the bases
are on the inside of the helix and the phosphates on the outside.
The configuration of the sugar and the atoms near it is close to
Furberg's 'standard configuration', the sugar being roughly
perpendicular to the attached base. There is a residue on each
every 3.4 A. in the z-direction. We have assumed an angle of 36° between adjacent residues in the same chain, so that the structure
repeats after 10 residues on each chain, that is, after 34 A. The
distance of a phosphorus atom from the fibre axis is 10 A. As the
phosphates are on the outside, cations have easy access to them.
The structure is an open one, and its water content is rather
Editorial process
AdminChecklist
EICAssignment
1
Mol ecul ar st r uct ur e of Nucl ei c Aci ds
WATSON, J. D. & CRICK, F. H. C.
Medical Research Council Unit for the Study of Molecular Structure
of Biological Systems, Cavendish Laboratory, Cambridge.
A St r uct ur e f or Deoxyr i bose Nucl ei c Aci d
We wish to suggest a structure for the salt of deoxyribose nucleic
acid (D.N.A.). This structure has novel features which are of
considerable biological interest.
A structure for nucleic acid has already been proposed by Pauling
and Corey1. They kindly made their manuscript available to us in
advance of publication. Their model consists of three intertwined
chains, with the phosphates near the fibre axis, and the bases on
the outside. In our opinion, this structure is unsatisfactory for
two reasons: (1) We believe that the material which gives the X-
ray diagrams is the salt, not the free acid. Without the acidic
hydrogen atoms it is not clear what forces would hold the
structure together, especially as the negatively charged
phosphates near the axis will repel each other. (2) Some of the
van der Waals distances appear to be too small.
Another three-chain structure has also been suggested by Fraser
(in the press). In his model the phosphates are on the outside and
the bases on the inside, linked together by hydrogen bonds. This
structure as described is rather ill-defined, and for this reason
we shall not comment on it.
We wish to put forward a radically different structure for the
salt of deoxyribose nucleic acid. This structure has two helical
chains each coiled round the same axis (see diagram). We have made
the usual chemical assumptions, namely, that each chain consists
of phosphate diester groups joining ß-D-deoxyribofuranose residues
with 3',5' linkages. The two chains (but not their bases) are
related by a dyad perpendicular to the fibre axis. Both chains
follow right- handed helices, but owing to the dyad the sequences
of the atoms in the two chains run in opposite directions. Each
chain loosely resembles Furberg's2 model No. 1; that is, the bases
are on the inside of the helix and the phosphates on the outside.
The configuration of the sugar and the atoms near it is close to
Furberg's 'standard configuration', the sugar being roughly
perpendicular to the attached base. There is a residue on each
every 3.4 A. in the z-direction. We have assumed an angle of 36° between adjacent residues in the same chain, so that the structure
repeats after 10 residues on each chain, that is, after 34 A. The
distance of a phosphorus atom from the fibre axis is 10 A. As the
phosphates are on the outside, cations have easy access to them.
The structure is an open one, and its water content is rather
Editorial process
AdminChecklist
EICAssignment
Editor Assignment
1
Mol ecul ar st r uct ur e of Nucl ei c Aci ds
WATSON, J. D. & CRICK, F. H. C.
Medical Research Council Unit for the Study of Molecular Structure
of Biological Systems, Cavendish Laboratory, Cambridge.
A St r uct ur e f or Deoxyr i bose Nucl ei c Aci d
We wish to suggest a structure for the salt of deoxyribose nucleic
acid (D.N.A.). This structure has novel features which are of
considerable biological interest.
A structure for nucleic acid has already been proposed by Pauling
and Corey1. They kindly made their manuscript available to us in
advance of publication. Their model consists of three intertwined
chains, with the phosphates near the fibre axis, and the bases on
the outside. In our opinion, this structure is unsatisfactory for
two reasons: (1) We believe that the material which gives the X-
ray diagrams is the salt, not the free acid. Without the acidic
hydrogen atoms it is not clear what forces would hold the
structure together, especially as the negatively charged
phosphates near the axis will repel each other. (2) Some of the
van der Waals distances appear to be too small.
Another three-chain structure has also been suggested by Fraser
(in the press). In his model the phosphates are on the outside and
the bases on the inside, linked together by hydrogen bonds. This
structure as described is rather ill-defined, and for this reason
we shall not comment on it.
We wish to put forward a radically different structure for the
salt of deoxyribose nucleic acid. This structure has two helical
chains each coiled round the same axis (see diagram). We have made
the usual chemical assumptions, namely, that each chain consists
of phosphate diester groups joining ß-D-deoxyribofuranose residues
with 3',5' linkages. The two chains (but not their bases) are
related by a dyad perpendicular to the fibre axis. Both chains
follow right- handed helices, but owing to the dyad the sequences
of the atoms in the two chains run in opposite directions. Each
chain loosely resembles Furberg's2 model No. 1; that is, the bases
are on the inside of the helix and the phosphates on the outside.
The configuration of the sugar and the atoms near it is close to
Furberg's 'standard configuration', the sugar being roughly
perpendicular to the attached base. There is a residue on each
every 3.4 A. in the z-direction. We have assumed an angle of 36° between adjacent residues in the same chain, so that the structure
repeats after 10 residues on each chain, that is, after 34 A. The
distance of a phosphorus atom from the fibre axis is 10 A. As the
phosphates are on the outside, cations have easy access to them.
The structure is an open one, and its water content is rather
Editorial process
AdminChecklist
EICAssignment
Editor Assignment
Referee
Invitation
Selection
Assignment
Scores
1
Mol ecul ar st r uct ur e of Nucl ei c Aci ds
WATSON, J. D. & CRICK, F. H. C.
Medical Research Council Unit for the Study of Molecular Structure
of Biological Systems, Cavendish Laboratory, Cambridge.
A St r uct ur e f or Deoxyr i bose Nucl ei c Aci d
We wish to suggest a structure for the salt of deoxyribose nucleic
acid (D.N.A.). This structure has novel features which are of
considerable biological interest.
A structure for nucleic acid has already been proposed by Pauling
and Corey1. They kindly made their manuscript available to us in
advance of publication. Their model consists of three intertwined
chains, with the phosphates near the fibre axis, and the bases on
the outside. In our opinion, this structure is unsatisfactory for
two reasons: (1) We believe that the material which gives the X-
ray diagrams is the salt, not the free acid. Without the acidic
hydrogen atoms it is not clear what forces would hold the
structure together, especially as the negatively charged
phosphates near the axis will repel each other. (2) Some of the
van der Waals distances appear to be too small.
Another three-chain structure has also been suggested by Fraser
(in the press). In his model the phosphates are on the outside and
the bases on the inside, linked together by hydrogen bonds. This
structure as described is rather ill-defined, and for this reason
we shall not comment on it.
We wish to put forward a radically different structure for the
salt of deoxyribose nucleic acid. This structure has two helical
chains each coiled round the same axis (see diagram). We have made
the usual chemical assumptions, namely, that each chain consists
of phosphate diester groups joining ß-D-deoxyribofuranose residues
with 3',5' linkages. The two chains (but not their bases) are
related by a dyad perpendicular to the fibre axis. Both chains
follow right- handed helices, but owing to the dyad the sequences
of the atoms in the two chains run in opposite directions. Each
chain loosely resembles Furberg's2 model No. 1; that is, the bases
are on the inside of the helix and the phosphates on the outside.
The configuration of the sugar and the atoms near it is close to
Furberg's 'standard configuration', the sugar being roughly
perpendicular to the attached base. There is a residue on each
every 3.4 A. in the z-direction. We have assumed an angle of 36° between adjacent residues in the same chain, so that the structure
repeats after 10 residues on each chain, that is, after 34 A. The
distance of a phosphorus atom from the fibre axis is 10 A. As the
phosphates are on the outside, cations have easy access to them.
The structure is an open one, and its water content is rather
Editorial process
AdminChecklist
EICAssignment
Editor Assignment
Referee
Invitation
Selection
Assignment
Scores
EditorRecommendation
1
Mol ecul ar st r uct ur e of Nucl ei c Aci ds
WATSON, J. D. & CRICK, F. H. C.
Medical Research Council Unit for the Study of Molecular Structure
of Biological Systems, Cavendish Laboratory, Cambridge.
A St r uct ur e f or Deoxyr i bose Nucl ei c Aci d
We wish to suggest a structure for the salt of deoxyribose nucleic
acid (D.N.A.). This structure has novel features which are of
considerable biological interest.
A structure for nucleic acid has already been proposed by Pauling
and Corey1. They kindly made their manuscript available to us in
advance of publication. Their model consists of three intertwined
chains, with the phosphates near the fibre axis, and the bases on
the outside. In our opinion, this structure is unsatisfactory for
two reasons: (1) We believe that the material which gives the X-
ray diagrams is the salt, not the free acid. Without the acidic
hydrogen atoms it is not clear what forces would hold the
structure together, especially as the negatively charged
phosphates near the axis will repel each other. (2) Some of the
van der Waals distances appear to be too small.
Another three-chain structure has also been suggested by Fraser
(in the press). In his model the phosphates are on the outside and
the bases on the inside, linked together by hydrogen bonds. This
structure as described is rather ill-defined, and for this reason
we shall not comment on it.
We wish to put forward a radically different structure for the
salt of deoxyribose nucleic acid. This structure has two helical
chains each coiled round the same axis (see diagram). We have made
the usual chemical assumptions, namely, that each chain consists
of phosphate diester groups joining ß-D-deoxyribofuranose residues
with 3',5' linkages. The two chains (but not their bases) are
related by a dyad perpendicular to the fibre axis. Both chains
follow right- handed helices, but owing to the dyad the sequences
of the atoms in the two chains run in opposite directions. Each
chain loosely resembles Furberg's2 model No. 1; that is, the bases
are on the inside of the helix and the phosphates on the outside.
The configuration of the sugar and the atoms near it is close to
Furberg's 'standard configuration', the sugar being roughly
perpendicular to the attached base. There is a residue on each
every 3.4 A. in the z-direction. We have assumed an angle of 36° between adjacent residues in the same chain, so that the structure
repeats after 10 residues on each chain, that is, after 34 A. The
distance of a phosphorus atom from the fibre axis is 10 A. As the
phosphates are on the outside, cations have easy access to them.
The structure is an open one, and its water content is rather
Editorial process
AdminChecklist
EICAssignment
Editor Assignment
Referee
Invitation
Selection
Assignment
Scores
EditorRecommendation
EIC decision
1
Mol ecul ar st r uct ur e of Nucl ei c Aci ds
WATSON, J. D. & CRICK, F. H. C.
Medical Research Council Unit for the Study of Molecular Structure
of Biological Systems, Cavendish Laboratory, Cambridge.
A St r uct ur e f or Deoxyr i bose Nucl ei c Aci d
We wish to suggest a structure for the salt of deoxyribose nucleic
acid (D.N.A.). This structure has novel features which are of
considerable biological interest.
A structure for nucleic acid has already been proposed by Pauling
and Corey1. They kindly made their manuscript available to us in
advance of publication. Their model consists of three intertwined
chains, with the phosphates near the fibre axis, and the bases on
the outside. In our opinion, this structure is unsatisfactory for
two reasons: (1) We believe that the material which gives the X-
ray diagrams is the salt, not the free acid. Without the acidic
hydrogen atoms it is not clear what forces would hold the
structure together, especially as the negatively charged
phosphates near the axis will repel each other. (2) Some of the
van der Waals distances appear to be too small.
Another three-chain structure has also been suggested by Fraser
(in the press). In his model the phosphates are on the outside and
the bases on the inside, linked together by hydrogen bonds. This
structure as described is rather ill-defined, and for this reason
we shall not comment on it.
We wish to put forward a radically different structure for the
salt of deoxyribose nucleic acid. This structure has two helical
chains each coiled round the same axis (see diagram). We have made
the usual chemical assumptions, namely, that each chain consists
of phosphate diester groups joining ß-D-deoxyribofuranose residues
with 3',5' linkages. The two chains (but not their bases) are
related by a dyad perpendicular to the fibre axis. Both chains
follow right- handed helices, but owing to the dyad the sequences
of the atoms in the two chains run in opposite directions. Each
chain loosely resembles Furberg's2 model No. 1; that is, the bases
are on the inside of the helix and the phosphates on the outside.
The configuration of the sugar and the atoms near it is close to
Furberg's 'standard configuration', the sugar being roughly
perpendicular to the attached base. There is a residue on each
every 3.4 A. in the z-direction. We have assumed an angle of 36° between adjacent residues in the same chain, so that the structure
repeats after 10 residues on each chain, that is, after 34 A. The
distance of a phosphorus atom from the fibre axis is 10 A. As the
phosphates are on the outside, cations have easy access to them.
The structure is an open one, and its water content is rather
Editorial process
AdminChecklist
EICAssignment
Editor Assignment
Referee
Invitation
Selection
Assignment
Scores
EditorRecommendation
EIC decision
RejectRevisionAccept
1
Mol ecul ar st r uct ur e of Nucl ei c Aci ds
WATSON, J. D. & CRICK, F. H. C.
Medical Research Council Unit for the Study of Molecular Structure
of Biological Systems, Cavendish Laboratory, Cambridge.
A St r uct ur e f or Deoxyr i bose Nucl ei c Aci d
We wish to suggest a structure for the salt of deoxyribose nucleic
acid (D.N.A.). This structure has novel features which are of
considerable biological interest.
A structure for nucleic acid has already been proposed by Pauling
and Corey1. They kindly made their manuscript available to us in
advance of publication. Their model consists of three intertwined
chains, with the phosphates near the fibre axis, and the bases on
the outside. In our opinion, this structure is unsatisfactory for
two reasons: (1) We believe that the material which gives the X-
ray diagrams is the salt, not the free acid. Without the acidic
hydrogen atoms it is not clear what forces would hold the
structure together, especially as the negatively charged
phosphates near the axis will repel each other. (2) Some of the
van der Waals distances appear to be too small.
Another three-chain structure has also been suggested by Fraser
(in the press). In his model the phosphates are on the outside and
the bases on the inside, linked together by hydrogen bonds. This
structure as described is rather ill-defined, and for this reason
we shall not comment on it.
We wish to put forward a radically different structure for the
salt of deoxyribose nucleic acid. This structure has two helical
chains each coiled round the same axis (see diagram). We have made
the usual chemical assumptions, namely, that each chain consists
of phosphate diester groups joining ß-D-deoxyribofuranose residues
with 3',5' linkages. The two chains (but not their bases) are
related by a dyad perpendicular to the fibre axis. Both chains
follow right- handed helices, but owing to the dyad the sequences
of the atoms in the two chains run in opposite directions. Each
chain loosely resembles Furberg's2 model No. 1; that is, the bases
are on the inside of the helix and the phosphates on the outside.
The configuration of the sugar and the atoms near it is close to
Furberg's 'standard configuration', the sugar being roughly
perpendicular to the attached base. There is a residue on each
every 3.4 A. in the z-direction. We have assumed an angle of 36° between adjacent residues in the same chain, so that the structure
repeats after 10 residues on each chain, that is, after 34 A. The
distance of a phosphorus atom from the fibre axis is 10 A. As the
phosphates are on the outside, cations have easy access to them.
The structure is an open one, and its water content is rather
Editorial process
AdminChecklist
EICAssignment
Editor Assignment
Referee
Invitation
Selection
Assignment
Scores
EditorRecommendation
EIC decision
RejectRevisionAccept
1
Mol ecul ar st r uct ur e of Nucl ei c Aci ds
WATSON, J. D. & CRICK, F. H. C.
Medical Research Council Unit for the Study of Molecular Structure
of Biological Systems, Cavendish Laboratory, Cambridge.
A St r uct ur e f or Deoxyr i bose Nucl ei c Aci d
We wish to suggest a structure for the salt of deoxyribose nucleic
acid (D.N.A.). This structure has novel features which are of
considerable biological interest.
A structure for nucleic acid has already been proposed by Pauling
and Corey1. They kindly made their manuscript available to us in
advance of publication. Their model consists of three intertwined
chains, with the phosphates near the fibre axis, and the bases on
the outside. In our opinion, this structure is unsatisfactory for
two reasons: (1) We believe that the material which gives the X-
ray diagrams is the salt, not the free acid. Without the acidic
hydrogen atoms it is not clear what forces would hold the
structure together, especially as the negatively charged
phosphates near the axis will repel each other. (2) Some of the
van der Waals distances appear to be too small.
Another three-chain structure has also been suggested by Fraser
(in the press). In his model the phosphates are on the outside and
the bases on the inside, linked together by hydrogen bonds. This
structure as described is rather ill-defined, and for this reason
we shall not comment on it.
We wish to put forward a radically different structure for the
salt of deoxyribose nucleic acid. This structure has two helical
chains each coiled round the same axis (see diagram). We have made
the usual chemical assumptions, namely, that each chain consists
of phosphate diester groups joining ß-D-deoxyribofuranose residues
with 3',5' linkages. The two chains (but not their bases) are
related by a dyad perpendicular to the fibre axis. Both chains
follow right- handed helices, but owing to the dyad the sequences
of the atoms in the two chains run in opposite directions. Each
chain loosely resembles Furberg's2 model No. 1; that is, the bases
are on the inside of the helix and the phosphates on the outside.
The configuration of the sugar and the atoms near it is close to
Furberg's 'standard configuration', the sugar being roughly
perpendicular to the attached base. There is a residue on each
every 3.4 A. in the z-direction. We have assumed an angle of 36° between adjacent residues in the same chain, so that the structure
repeats after 10 residues on each chain, that is, after 34 A. The
distance of a phosphorus atom from the fibre axis is 10 A. As the
phosphates are on the outside, cations have easy access to them.
The structure is an open one, and its water content is rather
Editorial process – times taken
AdminChecklist
EICAssignment
Editor Assignment
Referee
Invitation
Selection
Assignment
Scores
EditorRecommendation
EIC decision
RejectRevisionAccept
1
Mol ecul ar st r uct ur e of Nucl ei c Aci ds
WATSON, J. D. & CRICK, F. H. C.
Medical Research Council Unit for the Study of Molecular Structure
of Biological Systems, Cavendish Laboratory, Cambridge.
A St r uct ur e f or Deoxyr i bose Nucl ei c Aci d
We wish to suggest a structure for the salt of deoxyribose nucleic
acid (D.N.A.). This structure has novel features which are of
considerable biological interest.
A structure for nucleic acid has already been proposed by Pauling
and Corey1. They kindly made their manuscript available to us in
advance of publication. Their model consists of three intertwined
chains, with the phosphates near the fibre axis, and the bases on
the outside. In our opinion, this structure is unsatisfactory for
two reasons: (1) We believe that the material which gives the X-
ray diagrams is the salt, not the free acid. Without the acidic
hydrogen atoms it is not clear what forces would hold the
structure together, especially as the negatively charged
phosphates near the axis will repel each other. (2) Some of the
van der Waals distances appear to be too small.
Another three-chain structure has also been suggested by Fraser
(in the press). In his model the phosphates are on the outside and
the bases on the inside, linked together by hydrogen bonds. This
structure as described is rather ill-defined, and for this reason
we shall not comment on it.
We wish to put forward a radically different structure for the
salt of deoxyribose nucleic acid. This structure has two helical
chains each coiled round the same axis (see diagram). We have made
the usual chemical assumptions, namely, that each chain consists
of phosphate diester groups joining ß-D-deoxyribofuranose residues
with 3',5' linkages. The two chains (but not their bases) are
related by a dyad perpendicular to the fibre axis. Both chains
follow right- handed helices, but owing to the dyad the sequences
of the atoms in the two chains run in opposite directions. Each
chain loosely resembles Furberg's2 model No. 1; that is, the bases
are on the inside of the helix and the phosphates on the outside.
The configuration of the sugar and the atoms near it is close to
Furberg's 'standard configuration', the sugar being roughly
perpendicular to the attached base. There is a residue on each
every 3.4 A. in the z-direction. We have assumed an angle of 36° between adjacent residues in the same chain, so that the structure
repeats after 10 residues on each chain, that is, after 34 A. The
distance of a phosphorus atom from the fibre axis is 10 A. As the
phosphates are on the outside, cations have easy access to them.
The structure is an open one, and its water content is rather
3 - 4 d
3 - 4 d
3 - 4 d 14 d
≤ 7 d
Editorial process – times taken
AdminChecklist
EICAssignment
Editor Assignment
Referee
Invitation
Selection
Assignment
Scores
EditorRecommendation
EIC decision
RejectRevisionAccept
?
1
Mol ecul ar st r uct ur e of Nucl ei c Aci ds
WATSON, J. D. & CRICK, F. H. C.
Medical Research Council Unit for the Study of Molecular Structure
of Biological Systems, Cavendish Laboratory, Cambridge.
A St r uct ur e f or Deoxyr i bose Nucl ei c Aci d
We wish to suggest a structure for the salt of deoxyribose nucleic
acid (D.N.A.). This structure has novel features which are of
considerable biological interest.
A structure for nucleic acid has already been proposed by Pauling
and Corey1. They kindly made their manuscript available to us in
advance of publication. Their model consists of three intertwined
chains, with the phosphates near the fibre axis, and the bases on
the outside. In our opinion, this structure is unsatisfactory for
two reasons: (1) We believe that the material which gives the X-
ray diagrams is the salt, not the free acid. Without the acidic
hydrogen atoms it is not clear what forces would hold the
structure together, especially as the negatively charged
phosphates near the axis will repel each other. (2) Some of the
van der Waals distances appear to be too small.
Another three-chain structure has also been suggested by Fraser
(in the press). In his model the phosphates are on the outside and
the bases on the inside, linked together by hydrogen bonds. This
structure as described is rather ill-defined, and for this reason
we shall not comment on it.
We wish to put forward a radically different structure for the
salt of deoxyribose nucleic acid. This structure has two helical
chains each coiled round the same axis (see diagram). We have made
the usual chemical assumptions, namely, that each chain consists
of phosphate diester groups joining ß-D-deoxyribofuranose residues
with 3',5' linkages. The two chains (but not their bases) are
related by a dyad perpendicular to the fibre axis. Both chains
follow right- handed helices, but owing to the dyad the sequences
of the atoms in the two chains run in opposite directions. Each
chain loosely resembles Furberg's2 model No. 1; that is, the bases
are on the inside of the helix and the phosphates on the outside.
The configuration of the sugar and the atoms near it is close to
Furberg's 'standard configuration', the sugar being roughly
perpendicular to the attached base. There is a residue on each
every 3.4 A. in the z-direction. We have assumed an angle of 36° between adjacent residues in the same chain, so that the structure
repeats after 10 residues on each chain, that is, after 34 A. The
distance of a phosphorus atom from the fibre axis is 10 A. As the
phosphates are on the outside, cations have easy access to them.
The structure is an open one, and its water content is rather
3 - 4 d
3 - 4 d
3 - 4 d
≤ 7 d
Peer reviewers - 2017 (n = 1,671)
0
200
400
600
800
1000
1200
1400
1 2 3 4 5 6 7 8 9 10
Num
ber
of
revie
wers
Number of reviews done
Peer reviewers - 2017 (n = 1,671)
0
200
400
600
800
1000
1200
1400
1 2 3 4 5 6 7 8 9 10
Num
ber
of
revie
wers
Number of reviews done
Overall time to first decision - 2018
0
100
200
300
400
500
600
0 10 20 30 40 50 60 70 80 90 100 110 120 130 140
Fre
qu
en
cy
Days
Overall time to first decision - 2018
0
100
200
300
400
500
600
0 10 20 30 40 50 60 70 80 90 100 110 120 130 140
Fre
qu
en
cy
Days
Mean = 33.02 daysMedian = 29.50 days
Overall time to first decision - 2018
0
100
200
300
400
500
600
0 10 20 30 40 50 60 70 80 90 100 110 120 130 140
Fre
qu
en
cy
Days
90% ≤ 70 days
Status enquiries - 2018
0
5
10
15
20
25
30
35
1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30
Fre
qu
en
cy
Weeks after submission
Status enquiries - 2018
0
5
10
15
20
25
30
35
1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30
Fre
qu
en
cy
Weeks after submission
Too eager
Status enquiries - 2018
0
5
10
15
20
25
30
35
1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30
Fre
qu
en
cy
Weeks after submission
Quite right
Status enquiries - 2018
0
5
10
15
20
25
30
35
1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30
Fre
qu
en
cy
Weeks after submission
Too patient
Status enquiries - 2018
0
5
10
15
20
25
30
35
1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30
Fre
qu
en
cy
Weeks after submission
Too polite
Status enquiries - 2018
0
5
10
15
20
25
30
35
1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30
Fre
qu
en
cy
Weeks after submission
EDITORIAL MANAGER
Colin W. E. Drummond
JAC@BSAC.org.uk
contact
Challenges
Authorship
Journal of Antimicrobial ChemotherapyThe Journal of the British Society for Antimicrobial Chemotherapy
Peer review – author’s perspective
by Nick Kim, Massey University, Wellington http://theconversation.com
Peer review – reviewer’s perspective
Peer review – reviewer’s perspective
Peer review – reviewer’s perspective
Peer review – reviewer’s perspective
Authorship disputes
Challenges
Journal of Antimicrobial ChemotherapyThe Journal of the British Society for Antimicrobial Chemotherapy
Authorship disputes
Who should be first author…..
Obviously
me ‘cos I
need it to
boost my H-
index
Who should be first author…..
Rubbish. It
must be me
‘cos I am the
most senior!
Who should be first author…..
Duh! Didn’t I
do all the
work?
Who should be first author…..
Sigh!
I have so
given up the
will to live!
Personal metrics
Challenges
Journal of Antimicrobial ChemotherapyThe Journal of the British Society for Antimicrobial Chemotherapy
Publish or perish
Impact Factor 2017
citations 2016 + citations 2015
=
Publications 2016 + publications 2015
Journal Impact Factor - 2017
Measuring performance of the journal
Measuring performance of the journal
“While the Impact Factor provides a
useful measure to show JAC’s standing
among other similar journals it should
never be used for measuring a given
authors scientific contribution to the field.”
Plan S
Challenges
Journal of Antimicrobial ChemotherapyThe Journal of the British Society for Antimicrobial Chemotherapy
Plan S
Plan S
The key principle is as follows:
“After 1 January 2020
scientific publications on the
results from research funded
by public grants provided by
national and European
research councils and
funding bodies, must be
published in compliant Open
Access Journals or on
compliant Open Access
Platforms.”
Plan S
Brussels 20th February 2019
PRESS RELEASE
Over 600 individuals and
organisations provided feedback to
cOAlition S on the implementation
guidance of Plan S. Originating from
over 40 countries, respondents
providing feedback include
researchers, librarians and libraries,
publishers and editors, universities,
learned societies, research funders
and performers, and other
interested citizens and
organisations.
Current publishing models
https://www.nature.com/articles/d41586-018-06178-7
Current publishing models
https://www.nature.com/articles/d41586-018-06178-7
Plan S
OUP operates two different open access models:
• An optional open access model (Oxford Open) for the majority of our
journals. Please see the individual journal home pages to find out
whether they offer optional open access.
• OUP also publish fully open access journals
Plan S
Open access publication fees (excluding taxes)
Elsevier
International Journal of Antimicrobial Agents (Hybrid) USD 3000
BSAC
Journal of Antimicrobial Chemotherapy (Hybrid) USD 2800 - 3200
Plan S
Journal of Antimicrobial Cheotherapy
AcknowledgementsEditorial Office Colin Drummond
Clare Jeeves
Suzanne Brockhouse
Sarah Egberger
Roya Khatiblou
Journal team Senior Editors
Editors
Referees
BSAC Phil Howard
Chris Longshaw
Kate Gould
Tracey Guise
OUP Phil Bishop
Emma Welsh
J Peter DonnellyEditor-in-Chief
JAC Editorial Office | Griffin House | 53 Regent Place | Birmingham B1 3NJ | UK
Journal of Antimicrobial
ChemotherapyA Journal of the British Society for Antimicrobial Chemotherapy
JAC
Telephone +31-(0)24-663-5188Mobile +31-(0)64-116-9297e-mail p.donnelly@usa.net