Isotopes in Environmental and Health Studies
Basic Information
Isotopes in Environmental and Health Studies (IEHS) provides a unique forum for the wide application of isotopes in environmental processes and in life sciences with the emphasis on novel developments in isotope research of spatial and temporal wide scaled processes. The primary focus is on publishing isotope applications in the fields of; ecology, biogeochemistry, hydro-and hydrogeology, geology and geochemistry, stable isotope tracer techniques in soil, water, plants, animals and in the human body, isotope effects and tracer theory including mathematical modelling, novel methodical developments, diagnostic stable isotopes in medicine and health studies, environmental sources of ionizing radiation and its effects on living matter. IEHS publishes original research articles and review papers, short communications, technical notes, and book reviews. Contributions from conferences, scientific panel discussions, or project reports are mostly welcome and can be edited in special issues. The journal provides authors to publish their articles open access. Peer Review Policy All submitted manuscripts are subject to initial appraisal by the Editor. If found suitable for further consideration, papers are subject to peer review by independent, anonymous expert referees. All peer review is single anonymized. Publishing Ethics The Journal adheres to the highest standards of publishing ethics, with rigorous processes in place to ensure this is achieved. Taylor & Francis is a member of Committee on Publication Ethics (COPE) and utilises CrossCheck for all Journals. More information on our ethical standards and policies can be found here: http://authorservices.taylorandfrancis.com/ethics-for-authors/.
CiteScore
| Subject | Rank | Percentile |
|---|---|---|
Environmental ScienceGeneral Environmental Science |
118 / 233 | 49% |
Journal Statistics
Submission Information
Submission Website:
http://mc.manuscriptcentral.com/giehRelated Articles
An unprecedented lanthanide phosphinidene halide: synthesis, structure and reactivity
Peng Cui, Yaofeng Chen, Xin Xu, Jie Sun
DOI: 10.1039/B813075B
Light-activation of gene function in mammalian cells viaribozymes
Douglas D. Young, R. Aaron Garner, Jeffrey A. Yoder, Alexander Deiters
DOI: 10.1039/B819375D
Chemoenzymatic synthesis of chiral 4,4′-bipyridyls and their metal–organic frameworks
Lenuta Sbircea, Narain D. Sharma, William Clegg, Ross W. Harrington, Peter N. Horton, Michael B. Hursthouse, David C. Apperley, Derek R. Boyd, Stuart L. James
DOI: 10.1039/B812366G
Facile photoinduced charge separation through a cyanoacetylide bridge in a heterobimetallic Fe(ii)–Re(i) complex
Mark E. Smith, Emma L. Flynn, Mark A. Fox, Alexandre Trottier, Eckart Wrede, Dmitri S. Yufit, Judith A. K. Howard, Kate L. Ronayne, Michael Towrie, Anthony W. Parker, František Hartl, Paul J. Low
DOI: 10.1039/B811357B
A cavitand with a fluorous rim acts as an amine receptor
Richard J. Hooley, Per Restorp, Julius Rebek Jr
DOI: 10.1039/B814069C
Synthesis of tri- and tetraynes using a butadiynyl synthon
Khalid Azyat, Eike Jahnke, Trent Rankin, Rik R. Tykwinski
DOI: 10.1039/B816177A
Titanocene-catalyzed alkylative dimerization of vinylGrignard reagent using alkyl halides
Yuuki Fujii, Jun Terao, Yuichiro Kato, Nobuaki Kambe
DOI: 10.1039/B813596G
Palladium-catalysed direct synthesis of benzo[b]thiophenes from thioenols
Kiyofumi Inamoto, Yukari Arai, Kou Hiroya, Takayuki Doi
DOI: 10.1039/B811362A
Modular synthesis of multivalent glycoarchitectures and their unique selectin binding behavior
Ilona Papp, Jens Dernedde, Sven Enders, Rainer Haag
DOI: 10.1039/B813414F
Dynamic kinetic resolution of β-keto sulfonesvia asymmetric transfer hydrogenation
Zhenhua Ding, Jin Yang, Ting Wang, Zongxuan Shen, Yawen Zhang
DOI: 10.1039/B818257D
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