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Example of Frontiers in Ecology and Evolution format Example of Frontiers in Ecology and Evolution format Example of Frontiers in Ecology and Evolution format Example of Frontiers in Ecology and Evolution format Example of Frontiers in Ecology and Evolution format Example of Frontiers in Ecology and Evolution format Example of Frontiers in Ecology and Evolution format Example of Frontiers in Ecology and Evolution format Example of Frontiers in Ecology and Evolution format
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Example of Frontiers in Ecology and Evolution format Example of Frontiers in Ecology and Evolution format Example of Frontiers in Ecology and Evolution format Example of Frontiers in Ecology and Evolution format Example of Frontiers in Ecology and Evolution format Example of Frontiers in Ecology and Evolution format Example of Frontiers in Ecology and Evolution format Example of Frontiers in Ecology and Evolution format Example of Frontiers in Ecology and Evolution format
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Frontiers in Ecology and Evolution — Template for authors

Publisher: Frontiers Media
Categories Rank Trend in last 3 yrs
Ecology #111 of 400 down down by 36 ranks
Ecology, Evolution, Behavior and Systematics #183 of 647 down down by 44 ranks
journal-quality-icon Journal quality:
Good
calendar-icon Last 4 years overview: 1249 Published Papers | 4438 Citations
indexed-in-icon Indexed in: Scopus
last-updated-icon Last updated: 09/07/2020
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open access Open Access
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CiteRatio: 5.6
SJR: 1.167
SNIP: 1.297

Journal Performance & Insights

CiteRatio

SCImago Journal Rank (SJR)

Source Normalized Impact per Paper (SNIP)

A measure of average citations received per peer-reviewed paper published in the journal.

Measures weighted citations received by the journal. Citation weighting depends on the categories and prestige of the citing journal.

Measures actual citations received relative to citations expected for the journal's category.

3.6

20% from 2019

CiteRatio for Frontiers in Ecology and Evolution from 2016 - 2020
Year Value
2020 3.6
2019 3.0
2018 3.7
2017 4.0
graph view Graph view
table view Table view

1.317

20% from 2019

SJR for Frontiers in Ecology and Evolution from 2018 - 2020
Year Value
2020 1.317
2019 1.101
2018 0.861
graph view Graph view
table view Table view

1.196

20% from 2019

SNIP for Frontiers in Ecology and Evolution from 2017 - 2020
Year Value
2020 1.196
2019 1.0
2018 0.895
2017 1.027
graph view Graph view
table view Table view

insights Insights

  • CiteRatio of this journal has increased by 20% in last years.
  • This journal’s CiteRatio is in the top 10 percentile category.

insights Insights

  • SJR of this journal has increased by 20% in last years.
  • This journal’s SJR is in the top 10 percentile category.

insights Insights

  • SNIP of this journal has increased by 20% in last years.
  • This journal’s SNIP is in the top 10 percentile category.

Frontiers in Ecology and Evolution

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Frontiers Media

Frontiers in Ecology and Evolution

Approved by publishing and review experts on SciSpace, this template is built as per for Frontiers in Ecology and Evolution formatting guidelines as mentioned in Frontiers Media author instructions. The current version was created on 09 Jul 2020 and has been used by 359 authors to write and format their manuscripts to this journal.

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Last updated on
09 Jul 2020
i
Open Access
No
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Sherpa RoMEO Archiving Policy
Green faq
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Plagiarism Check
Available via Turnitin
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Endnote Style
Download Available
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Bibliography Name
frontiersinSCNS_ENG_HUMS
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Citation Type
Numbered
[25]
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Bibliography Example
Blonder GE, Tinkham M, Klapwijk TM. Transition from metallic to tunneling regimes in superconducting microconstrictions: Excess current, charge imbalance, and supercurrent conversion. Phys. Rev. B 25 (1982) 4515–4532.

Top papers written in this journal

open accessOpen access Journal Article DOI: 10.3389/FEVO.2015.00155
Linking Movement Ecology with Wildlife Management and Conservation
Andrew M. Allen1, Navinder J. Singh1

Abstract:

A common challenge in species conservation and management is how to incorporate species movements into management objectives. There often is a lack of knowledge of where, when and why species move. The field of movement ecology has grown rapidly in the last decade and is now providing the knowledge needed to incorporate movem... A common challenge in species conservation and management is how to incorporate species movements into management objectives. There often is a lack of knowledge of where, when and why species move. The field of movement ecology has grown rapidly in the last decade and is now providing the knowledge needed to incorporate movements of species into management planning. This knowledge can also be used to develop management strategies that are flexible in time and space and may improve the effectiveness of management actions. Therefore, wildlife management and conservation may benefit by strengthening the link with movement ecology. We present a framework that illustrates how animal movement can be used to enhance conservation planning and identify management actions that are complementary to existing strategies. The framework contains five steps that identify (1) the movement attributes of a species, (2) their impacts on ecosystems, (3) how this knowledge can be used to guide the scale and type of management, (4) the implementation, and (5) the evaluation of management actions. We discuss these five steps in detail, highlighting why the step is important and how the information can be obtained. We illustrate the framework through a case study of managing a highly mobile species, the Atlantic salmon (Salmo salar), a harvested species of conservation concern. We believe that the movement-management framework provides an important, and timely, link between movement ecology and wildlife management and conservation, and highlights the potential for complementary, dynamic solutions for managing wildlife. read more read less

Topics:

Ecosystem management (61%)61% related to the paper, Adaptive management (61%)61% related to the paper, Wildlife conservation (59%)59% related to the paper, Applied ecology (57%)57% related to the paper, Management by objectives (54%)54% related to the paper
View PDF
251 Citations
open accessOpen access Journal Article DOI: 10.3389/FEVO.2015.00065
Climate-adjusted provenancing: a strategy for climate-resilient ecological restoration

Abstract:

Investments in ecological restoration are estimated at $US 2 trillion per annum worldwide and are increasing rapidly ( Cunningham, 2008 ; Williams et al., 2014 ). These investments are occurring in an environment of accelerated climate change that is projected to continue into the next century, yet they currently take little ... Investments in ecological restoration are estimated at $US 2 trillion per annum worldwide and are increasing rapidly ( Cunningham, 2008 ; Williams et al., 2014 ). These investments are occurring in an environment of accelerated climate change that is projected to continue into the next century, yet they currently take little account of such change. This has significant implications for the long-term success of restoration plantings across millions of hectares, with germplasm used in current restoration efforts potentially poorly-adapted to future climates. New approaches that optimize the climate-resilience of these restoration efforts are thus essential ( Breed et al., 2013 ; Williams et al., 2014 ; Havens et al., 2015 ). A promising, but as yet untapped, opportunity for enhancing the climate-resilience of restoration investments rests in the exploitation of natural genetic variability of plant species. The capacity of plants to adapt to environmental change through plasticity, selection, or gene flow is only beginning to be explored ( Nicotra et al., 2010 ; Hoffmann and Sgro, 2011 ; Aitken and Whitlock, 2013 ; Alberto et al., 2013 ). Informed strategies for sourcing germplasm that capitalize on inherent genetic diversity and adaptive capacity offer significant promise for improving the success of extensive plantings to restore landscapes that are eroded, salinized, desertified, highly fragmented or degraded through introduced competitors, herbivores, or diseases. Here we describe a new strategy for sourcing germplasm for ecological restoration to promote adaptation in a changing climate. We argue that a "climate-adjusted" provenancing strategy (Figure 1A ) should combine genetic diversity and adaptability, targeting projected climate change directions whilst allowing for uncertainty in such projections as well as unforeseen selective agents. We introduce climate-adjusted provenancing in the context of historical approaches to provenancing, and highlight emerging research to test this strategy. read more read less

Topics:

Restoration ecology (54%)54% related to the paper, Adaptive capacity (52%)52% related to the paper
View PDF
238 Citations
open accessOpen access Journal Article DOI: 10.3389/FEVO.2018.00149
Modelling Palaeoecological Time Series Using Generalised Additive Models
Gavin Simpson1

Abstract:

In the absence of annual laminations, time series generated from lake sediments or other similar stratigraphic sequences are irregularly spaced in time, which complicates formal analysis using classical statistical time series models. In lieu, statistical analyses of trends in palaeoenvironmental time series, if done at all, ... In the absence of annual laminations, time series generated from lake sediments or other similar stratigraphic sequences are irregularly spaced in time, which complicates formal analysis using classical statistical time series models. In lieu, statistical analyses of trends in palaeoenvironmental time series, if done at all, have typically used simpler linear regressions or (non-) parametric correlations with little regard for the violation of assumptions that almost surely occurs due to temporal dependencies in the data or that correlations do not provide estimates of the magnitude of change, just whether or not there is a linear or monotonic trend. Alternative approaches have used LOESS-estimated trends to justify data interpretations or test hypotheses as to the causal factors without considering the inherent subjectivity of the choice of parameters used to achieve the LOESS fit (e.g. span width, degree of polynomial). Generalized additive models (GAMs) are statistical models that can be used to estimate trends as smooth functions of time. Unlike LOESS, GAMs use automatic smoothness selection methods to objectively determine the complexity of the fitted trend, and as formal statistical models, GAMs, allow for potentially complex, non-linear trends, a proper accounting of model uncertainty, and the identification of periods of significant temporal change. Here, I present a consistent and modern approach to the estimation of trends in palaeoenvironmental time series using GAMs, illustrating features of the methodology with two example time series of contrasting complexity; a 150-year bulk organic matter δ15N time series from Small Water, UK, and a 3000-year alkenone record from Braya-So, Greenland. I discuss the underlying mechanics of GAMs that allow them to learn the shape of the trend from the data themselves and how simultaneous confidence intervals and the first derivatives of the trend are used to properly account for model uncertainty and identify periods of change. It is hoped that by using GAMs greater attention is paid to the statistical estimation of trends in palaeoenvironmental time series leading to more a robust and reproducible palaeoscience. read more read less

Topics:

Statistical model (53%)53% related to the paper, Generalized additive model (53%)53% related to the paper, Additive model (50%)50% related to the paper, Parametric statistics (50%)50% related to the paper
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233 Citations
open accessOpen access Journal Article DOI: 10.3389/FEVO.2018.00165
Genetic Diversity and Conservation Units: Dealing With the Species-Population Continuum in the Age of Genomics
David J. Coates, Margaret Byrne, Craig Moritz1

Abstract:

Current approaches to biodiversity conservation are largely based on geographic areas, ecosystems, ecological communities and species, with less attention ongenetic diversity and the evolutionary continuum from populations to species. Conservation management generally rests on discrete categories, such as identified species, ... Current approaches to biodiversity conservation are largely based on geographic areas, ecosystems, ecological communities and species, with less attention ongenetic diversity and the evolutionary continuum from populations to species. Conservation management generally rests on discrete categories, such as identified species, and, for threated taxa, intraspecific units. Species, in particular, provide a common measure of biodiversity yet in both theory and nature, speciation is typically a protracted process progressing from connected populations to unambiguous species with variable rates of phenotypic, ecological and genetic divergence. Thus, most recognised species are not genetically uniform and are sometimes highly structured into historically isolated populations worthy of consideration as intraspecific units that represent unique genetic diversity for conservation. Genome screens offer unprecedented resolution of structure across taxonomic boundaries in species complexes, and have the potential to oversplit species if not interpreted conservatively. This highlights the blurred line between populations and species, and can confound simple dichotomies of ‘species’ versus ‘not species’. At the same time, like plants, there is increasing evidence than even distantly related animal species can hybridize and exchange genes. A review of conservation legislation reveals that legal definitions of ‘species’ are quite flexible and can accommodate a range of infra-specific taxa and divergent populations, as well as taxonomically recognised species. For example, the legislative definition of a species around the world can include: species, subspecies, varieties, and geographically and/or genetically distinct populations. In principle, this flexibility allows for protection of genetic diversity and maintenance of evolutionary processes at a broad range of infra-specific levels. However, evolutionary biologists often fail to adequately justify and then translate their evidence for genetically defined units into categories suited to assessment under local legislation. We recommend that (i). genomic data should be interpreted conservatively when formally naming species, (ii). concomitantly, there should be stronger impetus and a more uniform approach to identifying clearly justified intraspecific units, (iii). guidelines be developed for recognising and labelling intraspecific data that align with best scientific practice, and (iv). that the more nuanced view of species and speciation emerging from genomic analyses is communicated more effectively by scientists to decision makers. read more read less

Topics:

Genetic divergence (57%)57% related to the paper, Population (55%)55% related to the paper, Biodiversity (55%)55% related to the paper, Range (biology) (52%)52% related to the paper, Genetic diversity (51%)51% related to the paper
View PDF
226 Citations
open accessOpen access Journal Article DOI: 10.3389/FEVO.2014.00027
Phylogenetic insights into Andean plant diversification
Federico Luebert1, Federico Luebert2, Maximilian Weigend2

Abstract:

Andean orogeny is considered as one of the most important events for the developmentof current plant diversity in South America. We compare available phylogenetic studies anddivergence time estimates for plant lineages that may have diversified in response to Andeanorogeny. The influence of the Andes on plant diversification ... Andean orogeny is considered as one of the most important events for the developmentof current plant diversity in South America. We compare available phylogenetic studies anddivergence time estimates for plant lineages that may have diversified in response to Andeanorogeny. The influence of the Andes on plant diversification is separated into four major groups:The Andes as source of new high-elevation habitats, as a vicariant barrier, as a North-Southcorridor and as generator of new environmental conditions outside the Andes. Biogeographicalrelationships between the Andes and other regions are also considered. Divergence timeestimates indicate that high-elevation lineages originated and diversified during or after the majorphases of Andean uplift (Mid-Miocene to Pliocene), although there are some exceptions. Asexpected, Andean mid-elevation lineages tend to be older than high-elevation groups. Mostclades with disjunct distribution on both sides of the Andes diverged during Andean uplift.Inner-Andean clades also tend to have divergence time during or after Andean uplift. This isinterpreted as evidence of vicariance. Dispersal along the Andes has been shown to occur ineither direction, mostly dated after the Andean uplift. Divergence time estimates of plant groupsoutside the Andes encompass a wider range of ages, indicating that the Andes may not benecessarily the cause of these diversifications. The Andes are biogeographically related to allneighbouring areas, especially Central America, with floristic interchanges in both directionssince Early Miocene times. Direct biogeographical relationships between the Andes and otherdisjunct regions have also been shown in phylogenetic studies, especially with the easternBrazilian highlands and North America. The history of the Andean flora is complex and plantdiversification has been driven by a variety of processes, including environmental change,adaptation, and biotic interactions read more read less

Topics:

Andean orogeny (54%)54% related to the paper, Vicariance (51%)51% related to the paper
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221 Citations
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To be honest, the answer is no. The impact factor is one of the many elements that determine the quality of a journal. Few of these factors include review board, rejection rates, frequency of inclusion in indexes, and Eigenfactor. You need to assess all these factors before you make your final call.

13. What is Sherpa RoMEO Archiving Policy for Frontiers in Ecology and Evolution?

SHERPA/RoMEO Database

We extracted this data from Sherpa Romeo to help researchers understand the access level of this journal in accordance with the Sherpa Romeo Archiving Policy for Frontiers in Ecology and Evolution. The table below indicates the level of access a journal has as per Sherpa Romeo's archiving policy.

RoMEO Colour Archiving policy
Green Can archive pre-print and post-print or publisher's version/PDF
Blue Can archive post-print (ie final draft post-refereeing) or publisher's version/PDF
Yellow Can archive pre-print (ie pre-refereeing)
White Archiving not formally supported
FYI:
  1. Pre-prints as being the version of the paper before peer review and
  2. Post-prints as being the version of the paper after peer-review, with revisions having been made.

14. What are the most common citation types In Frontiers in Ecology and Evolution?

The 5 most common citation types in order of usage for Frontiers in Ecology and Evolution are:.

S. No. Citation Style Type
1. Author Year
2. Numbered
3. Numbered (Superscripted)
4. Author Year (Cited Pages)
5. Footnote

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Yes, SciSpace provides this functionality. After signing up, you would need to import your existing references from Word or Bib file to SciSpace. Then SciSpace would allow you to download your references in Frontiers in Ecology and Evolution Endnote style according to Elsevier guidelines.

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