This document summarizes the open access publication workflows at four Helmholtz research centers in Germany. It discusses the frame conditions for open access publishing, including agreements to make publications freely available. It then describes how each center implements open access, whether through central or decentralized funding of publication fees, and which publications are eligible for funding. Several centers fund publication fees through a central library fund, while one center leaves funding decentralized to research groups.
This presentation was used in the Open Access Week 2013. I organised a succesfull afternoon symposium at the TU DElft Library. My presentation was in overall introduction, so and others could go more into depth.
Subscription costs versus open access costs, & Dissolving journals' boundariesAlex Holcombe
draft of talk for Reclaiming the Knowledge Commons http://www.eventbrite.com.au/e/reclaiming-the-knowledge-commons-the-ethics-of-academic-publishing-and-the-futures-of-research-tickets-17560178968
Institutionalisation of an open access – a new possibility for research. A s...Birute Railiene
Birute Railiene. Institutionalisation of an open access – a new possibility for research : a survey of perception and demand
Paper for the 5th International Conference of the European Society of History of Science, Athens, 1-3 November 2012
This presentation was used in the Open Access Week 2013. I organised a succesfull afternoon symposium at the TU DElft Library. My presentation was in overall introduction, so and others could go more into depth.
Subscription costs versus open access costs, & Dissolving journals' boundariesAlex Holcombe
draft of talk for Reclaiming the Knowledge Commons http://www.eventbrite.com.au/e/reclaiming-the-knowledge-commons-the-ethics-of-academic-publishing-and-the-futures-of-research-tickets-17560178968
Institutionalisation of an open access – a new possibility for research. A s...Birute Railiene
Birute Railiene. Institutionalisation of an open access – a new possibility for research : a survey of perception and demand
Paper for the 5th International Conference of the European Society of History of Science, Athens, 1-3 November 2012
Presentation at the “Open Science: connecting the actors” event on the 21st of November 2022:
Share best practices, foster community, and encourage knowledge-sharing on Open Science.
At the heart of the Open Access Belgium community is the ambition to open up the way we organize and conduct scientific research.
The Open Science teams of the Belgian universities have developed and tested a wide range of training methods, training materials, networking activities
and data solutions to facilitate and foster Open Science. Achievements, tools and lessons learned by different institutions will be shared in this networking event.
Programme can be found here: https://openaccess.be/2022/10/04/open-science-connecting-the-actors/
Open Access has many advantages for an early carreer scientist including greater visibility, use of the research and even in many cases increased citations.
This factsheet is produced for the webinar Open Access for Global Climate Change Scientists 2011 ()
This talk gives an overview of current research data management practice with special emphasis on the role libraries can play as actors within larger information infrastructures. Such infrastructures are being increasingly summarized under the term Research Data Repositories (RDR).
[Sommer] [7 into 1. Integration and Collaboration: The new library for Humani...Diane Koen
Presentation made by [Dorothea Sommer] at the IFLA Library Buildings and Equipment Satellite Meeting. Illinois Institute of Technology, Chicago, Aug.10-11, 2016.
Chcete vědět víc? Mnoho dalších prezentací, videí z konferencí, fotografií i jiných dokumentů je k dispozici v institucionálním repozitáři NTK: http://repozitar.techlib.cz
Would you like to know more? Find presentations, reports, conference videos, photos and much more in our institutional repository at: http://repozitar.techlib.cz/?ln=en
Seminar of U.V. Spectroscopy by SAMIR PANDASAMIR PANDA
Spectroscopy is a branch of science dealing the study of interaction of electromagnetic radiation with matter.
Ultraviolet-visible spectroscopy refers to absorption spectroscopy or reflect spectroscopy in the UV-VIS spectral region.
Ultraviolet-visible spectroscopy is an analytical method that can measure the amount of light received by the analyte.
Cancer cell metabolism: special Reference to Lactate PathwayAADYARAJPANDEY1
Normal Cell Metabolism:
Cellular respiration describes the series of steps that cells use to break down sugar and other chemicals to get the energy we need to function.
Energy is stored in the bonds of glucose and when glucose is broken down, much of that energy is released.
Cell utilize energy in the form of ATP.
The first step of respiration is called glycolysis. In a series of steps, glycolysis breaks glucose into two smaller molecules - a chemical called pyruvate. A small amount of ATP is formed during this process.
Most healthy cells continue the breakdown in a second process, called the Kreb's cycle. The Kreb's cycle allows cells to “burn” the pyruvates made in glycolysis to get more ATP.
The last step in the breakdown of glucose is called oxidative phosphorylation (Ox-Phos).
It takes place in specialized cell structures called mitochondria. This process produces a large amount of ATP. Importantly, cells need oxygen to complete oxidative phosphorylation.
If a cell completes only glycolysis, only 2 molecules of ATP are made per glucose. However, if the cell completes the entire respiration process (glycolysis - Kreb's - oxidative phosphorylation), about 36 molecules of ATP are created, giving it much more energy to use.
IN CANCER CELL:
Unlike healthy cells that "burn" the entire molecule of sugar to capture a large amount of energy as ATP, cancer cells are wasteful.
Cancer cells only partially break down sugar molecules. They overuse the first step of respiration, glycolysis. They frequently do not complete the second step, oxidative phosphorylation.
This results in only 2 molecules of ATP per each glucose molecule instead of the 36 or so ATPs healthy cells gain. As a result, cancer cells need to use a lot more sugar molecules to get enough energy to survive.
Unlike healthy cells that "burn" the entire molecule of sugar to capture a large amount of energy as ATP, cancer cells are wasteful.
Cancer cells only partially break down sugar molecules. They overuse the first step of respiration, glycolysis. They frequently do not complete the second step, oxidative phosphorylation.
This results in only 2 molecules of ATP per each glucose molecule instead of the 36 or so ATPs healthy cells gain. As a result, cancer cells need to use a lot more sugar molecules to get enough energy to survive.
introduction to WARBERG PHENOMENA:
WARBURG EFFECT Usually, cancer cells are highly glycolytic (glucose addiction) and take up more glucose than do normal cells from outside.
Otto Heinrich Warburg (; 8 October 1883 – 1 August 1970) In 1931 was awarded the Nobel Prize in Physiology for his "discovery of the nature and mode of action of the respiratory enzyme.
WARNBURG EFFECT : cancer cells under aerobic (well-oxygenated) conditions to metabolize glucose to lactate (aerobic glycolysis) is known as the Warburg effect. Warburg made the observation that tumor slices consume glucose and secrete lactate at a higher rate than normal tissues.
More Related Content
Similar to Publication fees for open access journals
Presentation at the “Open Science: connecting the actors” event on the 21st of November 2022:
Share best practices, foster community, and encourage knowledge-sharing on Open Science.
At the heart of the Open Access Belgium community is the ambition to open up the way we organize and conduct scientific research.
The Open Science teams of the Belgian universities have developed and tested a wide range of training methods, training materials, networking activities
and data solutions to facilitate and foster Open Science. Achievements, tools and lessons learned by different institutions will be shared in this networking event.
Programme can be found here: https://openaccess.be/2022/10/04/open-science-connecting-the-actors/
Open Access has many advantages for an early carreer scientist including greater visibility, use of the research and even in many cases increased citations.
This factsheet is produced for the webinar Open Access for Global Climate Change Scientists 2011 ()
This talk gives an overview of current research data management practice with special emphasis on the role libraries can play as actors within larger information infrastructures. Such infrastructures are being increasingly summarized under the term Research Data Repositories (RDR).
[Sommer] [7 into 1. Integration and Collaboration: The new library for Humani...Diane Koen
Presentation made by [Dorothea Sommer] at the IFLA Library Buildings and Equipment Satellite Meeting. Illinois Institute of Technology, Chicago, Aug.10-11, 2016.
Chcete vědět víc? Mnoho dalších prezentací, videí z konferencí, fotografií i jiných dokumentů je k dispozici v institucionálním repozitáři NTK: http://repozitar.techlib.cz
Would you like to know more? Find presentations, reports, conference videos, photos and much more in our institutional repository at: http://repozitar.techlib.cz/?ln=en
Seminar of U.V. Spectroscopy by SAMIR PANDASAMIR PANDA
Spectroscopy is a branch of science dealing the study of interaction of electromagnetic radiation with matter.
Ultraviolet-visible spectroscopy refers to absorption spectroscopy or reflect spectroscopy in the UV-VIS spectral region.
Ultraviolet-visible spectroscopy is an analytical method that can measure the amount of light received by the analyte.
Cancer cell metabolism: special Reference to Lactate PathwayAADYARAJPANDEY1
Normal Cell Metabolism:
Cellular respiration describes the series of steps that cells use to break down sugar and other chemicals to get the energy we need to function.
Energy is stored in the bonds of glucose and when glucose is broken down, much of that energy is released.
Cell utilize energy in the form of ATP.
The first step of respiration is called glycolysis. In a series of steps, glycolysis breaks glucose into two smaller molecules - a chemical called pyruvate. A small amount of ATP is formed during this process.
Most healthy cells continue the breakdown in a second process, called the Kreb's cycle. The Kreb's cycle allows cells to “burn” the pyruvates made in glycolysis to get more ATP.
The last step in the breakdown of glucose is called oxidative phosphorylation (Ox-Phos).
It takes place in specialized cell structures called mitochondria. This process produces a large amount of ATP. Importantly, cells need oxygen to complete oxidative phosphorylation.
If a cell completes only glycolysis, only 2 molecules of ATP are made per glucose. However, if the cell completes the entire respiration process (glycolysis - Kreb's - oxidative phosphorylation), about 36 molecules of ATP are created, giving it much more energy to use.
IN CANCER CELL:
Unlike healthy cells that "burn" the entire molecule of sugar to capture a large amount of energy as ATP, cancer cells are wasteful.
Cancer cells only partially break down sugar molecules. They overuse the first step of respiration, glycolysis. They frequently do not complete the second step, oxidative phosphorylation.
This results in only 2 molecules of ATP per each glucose molecule instead of the 36 or so ATPs healthy cells gain. As a result, cancer cells need to use a lot more sugar molecules to get enough energy to survive.
Unlike healthy cells that "burn" the entire molecule of sugar to capture a large amount of energy as ATP, cancer cells are wasteful.
Cancer cells only partially break down sugar molecules. They overuse the first step of respiration, glycolysis. They frequently do not complete the second step, oxidative phosphorylation.
This results in only 2 molecules of ATP per each glucose molecule instead of the 36 or so ATPs healthy cells gain. As a result, cancer cells need to use a lot more sugar molecules to get enough energy to survive.
introduction to WARBERG PHENOMENA:
WARBURG EFFECT Usually, cancer cells are highly glycolytic (glucose addiction) and take up more glucose than do normal cells from outside.
Otto Heinrich Warburg (; 8 October 1883 – 1 August 1970) In 1931 was awarded the Nobel Prize in Physiology for his "discovery of the nature and mode of action of the respiratory enzyme.
WARNBURG EFFECT : cancer cells under aerobic (well-oxygenated) conditions to metabolize glucose to lactate (aerobic glycolysis) is known as the Warburg effect. Warburg made the observation that tumor slices consume glucose and secrete lactate at a higher rate than normal tissues.
Slide 1: Title Slide
Extrachromosomal Inheritance
Slide 2: Introduction to Extrachromosomal Inheritance
Definition: Extrachromosomal inheritance refers to the transmission of genetic material that is not found within the nucleus.
Key Components: Involves genes located in mitochondria, chloroplasts, and plasmids.
Slide 3: Mitochondrial Inheritance
Mitochondria: Organelles responsible for energy production.
Mitochondrial DNA (mtDNA): Circular DNA molecule found in mitochondria.
Inheritance Pattern: Maternally inherited, meaning it is passed from mothers to all their offspring.
Diseases: Examples include Leber’s hereditary optic neuropathy (LHON) and mitochondrial myopathy.
Slide 4: Chloroplast Inheritance
Chloroplasts: Organelles responsible for photosynthesis in plants.
Chloroplast DNA (cpDNA): Circular DNA molecule found in chloroplasts.
Inheritance Pattern: Often maternally inherited in most plants, but can vary in some species.
Examples: Variegation in plants, where leaf color patterns are determined by chloroplast DNA.
Slide 5: Plasmid Inheritance
Plasmids: Small, circular DNA molecules found in bacteria and some eukaryotes.
Features: Can carry antibiotic resistance genes and can be transferred between cells through processes like conjugation.
Significance: Important in biotechnology for gene cloning and genetic engineering.
Slide 6: Mechanisms of Extrachromosomal Inheritance
Non-Mendelian Patterns: Do not follow Mendel’s laws of inheritance.
Cytoplasmic Segregation: During cell division, organelles like mitochondria and chloroplasts are randomly distributed to daughter cells.
Heteroplasmy: Presence of more than one type of organellar genome within a cell, leading to variation in expression.
Slide 7: Examples of Extrachromosomal Inheritance
Four O’clock Plant (Mirabilis jalapa): Shows variegated leaves due to different cpDNA in leaf cells.
Petite Mutants in Yeast: Result from mutations in mitochondrial DNA affecting respiration.
Slide 8: Importance of Extrachromosomal Inheritance
Evolution: Provides insight into the evolution of eukaryotic cells.
Medicine: Understanding mitochondrial inheritance helps in diagnosing and treating mitochondrial diseases.
Agriculture: Chloroplast inheritance can be used in plant breeding and genetic modification.
Slide 9: Recent Research and Advances
Gene Editing: Techniques like CRISPR-Cas9 are being used to edit mitochondrial and chloroplast DNA.
Therapies: Development of mitochondrial replacement therapy (MRT) for preventing mitochondrial diseases.
Slide 10: Conclusion
Summary: Extrachromosomal inheritance involves the transmission of genetic material outside the nucleus and plays a crucial role in genetics, medicine, and biotechnology.
Future Directions: Continued research and technological advancements hold promise for new treatments and applications.
Slide 11: Questions and Discussion
Invite Audience: Open the floor for any questions or further discussion on the topic.
Earliest Galaxies in the JADES Origins Field: Luminosity Function and Cosmic ...Sérgio Sacani
We characterize the earliest galaxy population in the JADES Origins Field (JOF), the deepest
imaging field observed with JWST. We make use of the ancillary Hubble optical images (5 filters
spanning 0.4−0.9µm) and novel JWST images with 14 filters spanning 0.8−5µm, including 7 mediumband filters, and reaching total exposure times of up to 46 hours per filter. We combine all our data
at > 2.3µm to construct an ultradeep image, reaching as deep as ≈ 31.4 AB mag in the stack and
30.3-31.0 AB mag (5σ, r = 0.1” circular aperture) in individual filters. We measure photometric
redshifts and use robust selection criteria to identify a sample of eight galaxy candidates at redshifts
z = 11.5 − 15. These objects show compact half-light radii of R1/2 ∼ 50 − 200pc, stellar masses of
M⋆ ∼ 107−108M⊙, and star-formation rates of SFR ∼ 0.1−1 M⊙ yr−1
. Our search finds no candidates
at 15 < z < 20, placing upper limits at these redshifts. We develop a forward modeling approach to
infer the properties of the evolving luminosity function without binning in redshift or luminosity that
marginalizes over the photometric redshift uncertainty of our candidate galaxies and incorporates the
impact of non-detections. We find a z = 12 luminosity function in good agreement with prior results,
and that the luminosity function normalization and UV luminosity density decline by a factor of ∼ 2.5
from z = 12 to z = 14. We discuss the possible implications of our results in the context of theoretical
models for evolution of the dark matter halo mass function.
THE IMPORTANCE OF MARTIAN ATMOSPHERE SAMPLE RETURN.Sérgio Sacani
The return of a sample of near-surface atmosphere from Mars would facilitate answers to several first-order science questions surrounding the formation and evolution of the planet. One of the important aspects of terrestrial planet formation in general is the role that primary atmospheres played in influencing the chemistry and structure of the planets and their antecedents. Studies of the martian atmosphere can be used to investigate the role of a primary atmosphere in its history. Atmosphere samples would also inform our understanding of the near-surface chemistry of the planet, and ultimately the prospects for life. High-precision isotopic analyses of constituent gases are needed to address these questions, requiring that the analyses are made on returned samples rather than in situ.
Multi-source connectivity as the driver of solar wind variability in the heli...Sérgio Sacani
The ambient solar wind that flls the heliosphere originates from multiple
sources in the solar corona and is highly structured. It is often described
as high-speed, relatively homogeneous, plasma streams from coronal
holes and slow-speed, highly variable, streams whose source regions are
under debate. A key goal of ESA/NASA’s Solar Orbiter mission is to identify
solar wind sources and understand what drives the complexity seen in the
heliosphere. By combining magnetic feld modelling and spectroscopic
techniques with high-resolution observations and measurements, we show
that the solar wind variability detected in situ by Solar Orbiter in March
2022 is driven by spatio-temporal changes in the magnetic connectivity to
multiple sources in the solar atmosphere. The magnetic feld footpoints
connected to the spacecraft moved from the boundaries of a coronal hole
to one active region (12961) and then across to another region (12957). This
is refected in the in situ measurements, which show the transition from fast
to highly Alfvénic then to slow solar wind that is disrupted by the arrival of
a coronal mass ejection. Our results describe solar wind variability at 0.5 au
but are applicable to near-Earth observatories.
The increased availability of biomedical data, particularly in the public domain, offers the opportunity to better understand human health and to develop effective therapeutics for a wide range of unmet medical needs. However, data scientists remain stymied by the fact that data remain hard to find and to productively reuse because data and their metadata i) are wholly inaccessible, ii) are in non-standard or incompatible representations, iii) do not conform to community standards, and iv) have unclear or highly restricted terms and conditions that preclude legitimate reuse. These limitations require a rethink on data can be made machine and AI-ready - the key motivation behind the FAIR Guiding Principles. Concurrently, while recent efforts have explored the use of deep learning to fuse disparate data into predictive models for a wide range of biomedical applications, these models often fail even when the correct answer is already known, and fail to explain individual predictions in terms that data scientists can appreciate. These limitations suggest that new methods to produce practical artificial intelligence are still needed.
In this talk, I will discuss our work in (1) building an integrative knowledge infrastructure to prepare FAIR and "AI-ready" data and services along with (2) neurosymbolic AI methods to improve the quality of predictions and to generate plausible explanations. Attention is given to standards, platforms, and methods to wrangle knowledge into simple, but effective semantic and latent representations, and to make these available into standards-compliant and discoverable interfaces that can be used in model building, validation, and explanation. Our work, and those of others in the field, creates a baseline for building trustworthy and easy to deploy AI models in biomedicine.
Bio
Dr. Michel Dumontier is the Distinguished Professor of Data Science at Maastricht University, founder and executive director of the Institute of Data Science, and co-founder of the FAIR (Findable, Accessible, Interoperable and Reusable) data principles. His research explores socio-technological approaches for responsible discovery science, which includes collaborative multi-modal knowledge graphs, privacy-preserving distributed data mining, and AI methods for drug discovery and personalized medicine. His work is supported through the Dutch National Research Agenda, the Netherlands Organisation for Scientific Research, Horizon Europe, the European Open Science Cloud, the US National Institutes of Health, and a Marie-Curie Innovative Training Network. He is the editor-in-chief for the journal Data Science and is internationally recognized for his contributions in bioinformatics, biomedical informatics, and semantic technologies including ontologies and linked data.
Introduction:
RNA interference (RNAi) or Post-Transcriptional Gene Silencing (PTGS) is an important biological process for modulating eukaryotic gene expression.
It is highly conserved process of posttranscriptional gene silencing by which double stranded RNA (dsRNA) causes sequence-specific degradation of mRNA sequences.
dsRNA-induced gene silencing (RNAi) is reported in a wide range of eukaryotes ranging from worms, insects, mammals and plants.
This process mediates resistance to both endogenous parasitic and exogenous pathogenic nucleic acids, and regulates the expression of protein-coding genes.
What are small ncRNAs?
micro RNA (miRNA)
short interfering RNA (siRNA)
Properties of small non-coding RNA:
Involved in silencing mRNA transcripts.
Called “small” because they are usually only about 21-24 nucleotides long.
Synthesized by first cutting up longer precursor sequences (like the 61nt one that Lee discovered).
Silence an mRNA by base pairing with some sequence on the mRNA.
Discovery of siRNA?
The first small RNA:
In 1993 Rosalind Lee (Victor Ambros lab) was studying a non- coding gene in C. elegans, lin-4, that was involved in silencing of another gene, lin-14, at the appropriate time in the
development of the worm C. elegans.
Two small transcripts of lin-4 (22nt and 61nt) were found to be complementary to a sequence in the 3' UTR of lin-14.
Because lin-4 encoded no protein, she deduced that it must be these transcripts that are causing the silencing by RNA-RNA interactions.
Types of RNAi ( non coding RNA)
MiRNA
Length (23-25 nt)
Trans acting
Binds with target MRNA in mismatch
Translation inhibition
Si RNA
Length 21 nt.
Cis acting
Bind with target Mrna in perfect complementary sequence
Piwi-RNA
Length ; 25 to 36 nt.
Expressed in Germ Cells
Regulates trnasposomes activity
MECHANISM OF RNAI:
First the double-stranded RNA teams up with a protein complex named Dicer, which cuts the long RNA into short pieces.
Then another protein complex called RISC (RNA-induced silencing complex) discards one of the two RNA strands.
The RISC-docked, single-stranded RNA then pairs with the homologous mRNA and destroys it.
THE RISC COMPLEX:
RISC is large(>500kD) RNA multi- protein Binding complex which triggers MRNA degradation in response to MRNA
Unwinding of double stranded Si RNA by ATP independent Helicase
Active component of RISC is Ago proteins( ENDONUCLEASE) which cleave target MRNA.
DICER: endonuclease (RNase Family III)
Argonaute: Central Component of the RNA-Induced Silencing Complex (RISC)
One strand of the dsRNA produced by Dicer is retained in the RISC complex in association with Argonaute
ARGONAUTE PROTEIN :
1.PAZ(PIWI/Argonaute/ Zwille)- Recognition of target MRNA
2.PIWI (p-element induced wimpy Testis)- breaks Phosphodiester bond of mRNA.)RNAse H activity.
MiRNA:
The Double-stranded RNAs are naturally produced in eukaryotic cells during development, and they have a key role in regulating gene expression .
Observation of Io’s Resurfacing via Plume Deposition Using Ground-based Adapt...Sérgio Sacani
Since volcanic activity was first discovered on Io from Voyager images in 1979, changes
on Io’s surface have been monitored from both spacecraft and ground-based telescopes.
Here, we present the highest spatial resolution images of Io ever obtained from a groundbased telescope. These images, acquired by the SHARK-VIS instrument on the Large
Binocular Telescope, show evidence of a major resurfacing event on Io’s trailing hemisphere. When compared to the most recent spacecraft images, the SHARK-VIS images
show that a plume deposit from a powerful eruption at Pillan Patera has covered part
of the long-lived Pele plume deposit. Although this type of resurfacing event may be common on Io, few have been detected due to the rarity of spacecraft visits and the previously low spatial resolution available from Earth-based telescopes. The SHARK-VIS instrument ushers in a new era of high resolution imaging of Io’s surface using adaptive
optics at visible wavelengths.
This pdf is about the Schizophrenia.
For more details visit on YouTube; @SELF-EXPLANATORY;
https://www.youtube.com/channel/UCAiarMZDNhe1A3Rnpr_WkzA/videos
Thanks...!
1. Helmholtz Open Access Workshop, 10-11 June 2013
Mitglied der Helmholtz-GemeinschaftSeite 1
Edith Reschke| HZDR, Bibliothek| www.hzdr.de
Publication fees for open access
journals – work flows at Helmholtz
Centres
Source: Wikipedia
2. Helmholtz Open Access Workshop, 10-11 June 2013
Mitglied der Helmholtz-GemeinschaftSeite 2
Edith Reschke| HZDR, Bibliothek| www.hzdr.de
AGENDA
1. Frame conditions
2. Implementation in Helmholtz Centres
3. Funding Open Access – but how? Praxis examples
Publication fees for open access journals – work flows at Helmholtz Centres
3. Helmholtz Open Access Workshop, 10-11 June 2013
Mitglied der Helmholtz-GemeinschaftSeite 3
Edith Reschke| HZDR, Bibliothek| www.hzdr.de
1.Frame conditions
22.10.2003 – Berlin Declaration on Open Access to Knowledge in the
Sciences and Humanities.
27.09.2004 - Agreement of the Assembly of Members: ”Publications from the
Helmholtz Association shall in future, without exception, be available free of
charge, in so fare no conflicting Agreement with the publishers or others
exists.”
Rules for good scientific practice (Regeln guter wissenschaftlicher Praxis)
Recommendations of the Deutsche Forschungsgemeinschaft „Vorschläge
zur Sicherung guter wissenschaftlicher Praxis“
Regulation for publication according to the Helmholtz Center
4. Helmholtz Open Access Workshop, 10-11 June 2013
Mitglied der Helmholtz-GemeinschaftSeite 4
Edith Reschke| HZDR, Bibliothek| www.hzdr.de
2. Implementation in Helmholtz Centres
Within the publication process there is one point more:
Publication fees for Open Access publications
Ways to organize the funding:
Central publication fund, administraded by the library (or by other departments)
Decentral funding by the scientific units
No funding at all
Conditions for funding by the Helmholtz Centres should be:
Corresponding author must be a member of the Helmholtz Center
Journal must be a Gold Open Access Journal, not a hybrid journal
No budget is available within a project
5. Helmholtz Open Access Workshop, 10-11 June 2013
Mitglied der Helmholtz-GemeinschaftSeite 5
Edith Reschke| HZDR, Bibliothek| www.hzdr.de
3. Funding Open Access – but how? 4 Praxis examples
3.1. Deutsches Elektronen-Synchrotron DESY Hamburg
3.2. Forschungszentrum Jülich
3.3. GSI Helmholtzzentrum für Schwerionenforschung
Darmstadt
3.4. Helmholtz-Zentrum Dresden – Rossendorf
Hermann von Helmholtz
(1821 – 1894)
6. Helmholtz Open Access Workshop, 10-11 June 2013
Mitglied der Helmholtz-GemeinschaftSeite 6
Edith Reschke| HZDR, Bibliothek| www.hzdr.de
3.1. Deutsches Elektronen-Synchrotron DESY Hamburg
Text and photos by Dr. M. Köhler
In accordance with the “Berlin Declaration on Open Access to
Knowledge in the Sciences and Humanities” DESY supports the open
access movement.
Rules for good scientific practice (Regeln guter wissenschaftlicher Praxis)
Recommendations of the DFG „Vorschläge zur Sicherung guter
wissenschaftlicher Praxis“
Regulations for publication according to DESY operational procedures
and company rules (Geschäfts- und Betriebsordnung GO/BO)
apply for all DESY staff members,
and to all guests who use the DESY facilities.
7. Helmholtz Open Access Workshop, 10-11 June 2013
Mitglied der Helmholtz-GemeinschaftSeite 7
Edith Reschke| HZDR, Bibliothek| www.hzdr.de
3.1. Deutsches Elektronen-Synchrotron DESY Hamburg
Decision of the Directorate on August 25th, 2006
All scientists at DESY are asked to
transfer preprints of their approved publications to publicly accessible electronic
print archives,
preferably publish in open access journals,
see to it that, when submitting articles for publication in other journals, DESY
retains the right to make the article accessible in its latest version and in
electronically readable form, e.g. in an institutional repository.
The DESY makes its own publications accessible to the public in an
institutional repository.
Adequate fees for the publication in open access journals will be accepted by
DESY.
The Library administered the OA publication fund of DESY.
Text by Dr. Martin Köhler
8. Helmholtz Open Access Workshop, 10-11 June 2013
Mitglied der Helmholtz-GemeinschaftSeite 8
Edith Reschke| HZDR, Bibliothek| www.hzdr.de
Publication Guidelines of Forschungszentrum Jülich GmbH
(Veröffentlichungsrichtlinie) since ~1960s, new ed. 01/2013
Rules of good scientific practice
Data archival
Approval of publications:
Singed prior to publication (institute directors, authors)
Agree to follow good scientific practice
No conflicts with possible patenting
Appropriate data archival
Publishing house
3.2. Publishing @ Jülich: Framework
Text by Dr. A. Wagner
9. Helmholtz Open Access Workshop, 10-11 June 2013
Mitglied der Helmholtz-GemeinschaftSeite 9
Edith Reschke| HZDR, Bibliothek| www.hzdr.de
Guideline 01/2013
Now mandantory:
Open Access for all publications of the publishing house JuSER:
Service of the library
Preprint of every paper for Open Access and archiving
Final version PDF for archiving
Funding via library
Corresponding Author is from FZ Jülich
Gold Open Access Journal (no hybrids)
All other charges involved
Central funding of all electronic and print publications as a
library service
3.2. Publishing @ Jülich: Framework
Text by Dr. Wagner
(http://bit.ly/10UXKMg)
10. Helmholtz Open Access Workshop, 10-11 June 2013
Mitglied der Helmholtz-GemeinschaftSeite 10
Edith Reschke| HZDR, Bibliothek| www.hzdr.de
3.3. Publication workflows @ GSI
The library supports the publication process especially to:
Service to the GSI institutional repository (in approval; OA visibility)
Services to metadata for the GSI institutional repository and the
evaluations
Advisory service (copy rights, image rights...) in connection to the
legal department
Information to open access (esp. questions to the Helmholtz
contracts)
Handling of supplementary materials (program code...)
Handling of receipts (only in cased of missing groups‘ regulations)
Green OA via Alliance licences is considered in close connection to
the library of FZ Jülich
No central OA funding
Text by Katrin Grosse
11. Helmholtz Open Access Workshop, 10-11 June 2013
Mitglied der Helmholtz-GemeinschaftSeite 11
Edith Reschke| HZDR, Bibliothek| www.hzdr.de
HZDR Board decision 06.04.2011:
OA publication fees have to be paid by project fund and if not available by the
central publication fund, administrated by the library.
The author decides to publish in Open Access.
The author requestes the absorption of costs.
Complete electronic workflow : publication database of HZDR
3.4. Helmholtz-Zentrum Dresden - Rossendorf
12. Helmholtz Open Access Workshop, 10-11 June 2013
Mitglied der Helmholtz-GemeinschaftSeite 12
Edith Reschke| HZDR, Bibliothek| www.hzdr.de
3.4. Helmholtz-Zentrum Dresden - Rossendorf
Approval of cost covering:
Corresponding author is from HZDR
The journal is a Gold Open Access Journal (no hybrid).
Absorption of cost
Department „Research Programs and International Projects“
checked whether project budget is available. If yes fees paid by
project budget
If a project budget is not available and for all other publications the
library absorps the OA publishing fees.
Central OA funding as a library service
13. Helmholtz Open Access Workshop, 10-11 June 2013
Mitglied der Helmholtz-GemeinschaftSeite 13
Edith Reschke| HZDR, Bibliothek| www.hzdr.de
Information technology
Scientist Research Programs and
International Projects
Library
3.4. Helmholtz-Zentrum Dresden - Rossendorf
14. Helmholtz Open Access Workshop, 10-11 June 2013
Mitglied der Helmholtz-GemeinschaftSeite 14
Edith Reschke| HZDR, Bibliothek| www.hzdr.de
Thank you for your attention.
Publication fees for open access journals – work flows at Helmholtz Centres
Edith Reschke
Helmholtz-Zentrum Dresden-Rossendorf
e.reschke@hzdr.de
http://www.hzdr.de