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Example of The Botanical Review format Example of The Botanical Review format Example of The Botanical Review format Example of The Botanical Review format Example of The Botanical Review format Example of The Botanical Review format Example of The Botanical Review format Example of The Botanical Review format Example of The Botanical Review format Example of The Botanical Review format Example of The Botanical Review format Example of The Botanical Review format Example of The Botanical Review format Example of The Botanical Review format Example of The Botanical Review format Example of The Botanical Review format Example of The Botanical Review format Example of The Botanical Review format
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The Botanical Review — Template for authors

Publisher: Springer
Categories Rank Trend in last 3 yrs
Plant Science #94 of 445 down down by 15 ranks
Ecology, Evolution, Behavior and Systematics #148 of 647 down down by 6 ranks
journal-quality-icon Journal quality:
High
calendar-icon Last 4 years overview: 54 Published Papers | 218 Citations
indexed-in-icon Indexed in: Scopus
last-updated-icon Last updated: 17/06/2020
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Related Journals

open access Open Access

Springer

Quality:  
High
CiteRatio: 4.0
SJR: 0.875
SNIP: 0.949
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Quality:  
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CiteRatio: 6.1
SJR: 1.095
SNIP: 1.178
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Elsevier

Quality:  
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CiteRatio: 5.1
SJR: 1.25
SNIP: 1.213

Journal Performance & Insights

Impact Factor

CiteRatio

Determines the importance of a journal by taking a measure of frequency with which the average article in a journal has been cited in a particular year.

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

1.667

34% from 2018

Impact factor for The Botanical Review from 2016 - 2019
Year Value
2019 1.667
2018 2.536
2017 2.5
2016 2.769
graph view Graph view
table view Table view

4.0

17% from 2019

CiteRatio for The Botanical Review from 2016 - 2020
Year Value
2020 4.0
2019 4.8
2018 5.0
2017 3.9
2016 3.3
graph view Graph view
table view Table view

insights Insights

  • Impact factor of this journal has decreased by 34% in last year.
  • This journal’s impact factor is in the top 10 percentile category.

insights Insights

  • CiteRatio of this journal has decreased by 17% in last years.
  • This journal’s CiteRatio is in the top 10 percentile category.

SCImago Journal Rank (SJR)

Source Normalized Impact per Paper (SNIP)

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.

0.848

18% from 2019

SJR for The Botanical Review from 2016 - 2020
Year Value
2020 0.848
2019 0.716
2018 0.878
2017 0.708
2016 0.719
graph view Graph view
table view Table view

1.375

23% from 2019

SNIP for The Botanical Review from 2016 - 2020
Year Value
2020 1.375
2019 1.118
2018 1.374
2017 1.146
2016 1.533
graph view Graph view
table view Table view

insights Insights

  • SJR of this journal has increased by 18% in last years.
  • This journal’s SJR is in the top 10 percentile category.

insights Insights

  • SNIP of this journal has increased by 23% in last years.
  • This journal’s SNIP is in the top 10 percentile category.

The Botanical Review

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Springer

The Botanical Review

For over half a century, The Botanical Review has been a leading international journal noted for its in-depth articles on a broad spectrum of botanical fields. Systematics, phytogeography, cladistics, evolution, physiology, ecology, morphology, paleobotany, and anatomy are but...... Read More

i
Last updated on
17 Jun 2020
i
ISSN
0006-8101
i
Impact Factor
High - 1.423
i
Open Access
No
i
Sherpa RoMEO Archiving Policy
Green faq
i
Plagiarism Check
Available via Turnitin
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Endnote Style
Download Available
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Bibliography Name
SPBASIC
i
Citation Type
Author Year
(Blonder et al, 1982)
i
Bibliography Example
Beenakker CWJ (2006) Specular andreev reflection in graphene. Phys Rev Lett 97(6):067,007, URL 10.1103/PhysRevLett.97.067007

Top papers written in this journal

Journal Article DOI: 10.1007/BF02912621
Positive interactions among plants
Ragan M. Callaway1
01 Oct 1995 - Botanical Review

Abstract:

Experimental evidence for positive interactions, or facilitation, among plants has increased markedly during the last 10 years. Experiments documenting facilitation have been conducted in many diverse ecological systems, which suggests that positive interactions may be fundamental processes in plant communities. Here, I revie... Experimental evidence for positive interactions, or facilitation, among plants has increased markedly during the last 10 years. Experiments documenting facilitation have been conducted in many diverse ecological systems, which suggests that positive interactions may be fundamental processes in plant communities. Here, I review the evidence for facilitation, the mechanisms by which facilitation operates, and the effects facilitation has on community structure. Facilitative mechanisms may act simultaneously with resource competition or allelopathy, and the overall effect of one species on another may be the product of multiple, complex interactions. Positive interactions may also determine community spatial patterns, permit coexistence, enhance diversity and productivity, and drive community dynamics. Once viewed as anecdotal and idiosyncratic, facilitation is now contributing to a more complete understanding of community structure and dynamics. read more read less

Topics:

Facilitation (61%)61% related to the paper
1,577 Citations
Journal Article DOI: 10.1007/BF02858763
Plant litter : its dynamics and effects on plant community structure
José M. Facelli1, Steward T. A. Pickett1
01 Jan 1991 - Botanical Review

Abstract:

We discuss the dynamics of plant litter, the effects of litter on the chemical and physical environment, the direct and indirect effects of plant litter on plant populations and communities, and different adaptative traits that may be related to litter accumulation. The production of litter depends primarily on the site produ... We discuss the dynamics of plant litter, the effects of litter on the chemical and physical environment, the direct and indirect effects of plant litter on plant populations and communities, and different adaptative traits that may be related to litter accumulation. The production of litter depends primarily on the site productivity, but other properties of the environment, as well as chance, may introduce important variation. The existence of time lags between the production of plant organs and their transformation into litter appears as a relevant character of litter dynamics seldom included in models. Herbivory, and other processes that destroy biomass or reduce productivity, may reduce the amount of litter produced. The destruction of litter encompasses a complex of interactions. The main processes, including physical and chemical degradation, consumption by invertebrates and decomposition, are differentially affected by the environment and by the physical and chemical characteristics of the litter itself. The relative importance of those processes varies among systems. read more read less

Topics:

Plant litter (69%)69% related to the paper, Litter (58%)58% related to the paper
1,437 Citations
Journal Article DOI: 10.1663/0006-8101(2006)72[1:DADOFS]2.0.CO;2
Diversity and Distribution of Floral Scent
Jette T. Knudsen1, Roger Eriksson2, Jonathan Gershenzon3, Bertil Ståhl
01 Mar 2006 - Botanical Review

Abstract:

A list of 1719 chemical compounds identified from headspace samples of floral scent is presented. The list has been compiled from some 270 published papers, including analyses of 991 species of flowering plants and a few gymnosperms, a sample including seed plants from 90 families and 38 orders. The compounds belong to seven ... A list of 1719 chemical compounds identified from headspace samples of floral scent is presented. The list has been compiled from some 270 published papers, including analyses of 991 species of flowering plants and a few gymnosperms, a sample including seed plants from 90 families and 38 orders. The compounds belong to seven major compound classes, of which the aliphatics, the benzenoids and phenylpropanoids, and, among the terpenes, the mono- and sesquiterpenes, occur in most orders of seeds plants. C5-branched compounds, irregular terpenes, nitrogen-containing compounds, and a class of miscellaneous cyclic compounds have been recorded in about two-thirds of the orders. Sulfur-containing compounds occur in a third of the orders, whereas diterpenes have been reported from three orders only. The most common single compounds in floral scent are the monoterpenes limonene, (E)-β-ocimene, myrcene, linalool, α- and β-pinene, and the benzenoids benzaldehyde, methyl 2-hydroxybenzoate (methyl salicylate), benzyl alcohol, and 2-phenyl ethanol, which occur in 54–71% of the families investigated so far. The sesquiterpene caryophyllene and the irregular terpene 6-methyl-5-hepten-2-one are also common and occur in more than 50% of the families. Orchidaceae are by far the best investigated family, followed by several families known to have many species with strongly scented flowers, such as Araceae, Arecaceae, Magnoliaceae, and Rosaceae. However, the majority of angiosperm families are still poorly investigated. Relationships between floral scent and pollination, chemistry, evolution, and phylogeny are briefly discussed. It is concluded that floral scent chemistry is of little use for phylogenetic estimates above the genus level, whereas the distribution and combinations of floral scent compounds at species and subspecific levels is a promising field of investigation for the understanding of adaptations and evolutionary processes in angiosperms. read more read less

Topics:

Linalool (51%)51% related to the paper, Terpene (50%)50% related to the paper
View PDF
1,172 Citations
Journal Article DOI: 10.1007/BF02859158
The cerrado vegetation of Brazil
George Eiten1
01 Apr 1972 - Botanical Review

Abstract:

XIV. XV. XVI. XVII. I. Cerrado as a vegetational province . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 201 II. Geographic location .............................................................................. 203 Inadequacy of vegetation maps . . . . . . . . . . . . . . ... XIV. XV. XVI. XVII. I. Cerrado as a vegetational province . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 201 II. Geographic location .............................................................................. 203 Inadequacy of vegetation maps . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 205 III. Physiognomy of individual plants and floristie composition .................. 210 IV. Tortuosity of cerrado trees and shrubs ..................................................... 221 V. Structural categories and terminology ................................................... 225 VI. Structural categories and floristic composition ....................................... 24l VII. Climate . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 242 Temperature . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 243 Rainfall ...................................................................................... 244 VIII. Substrate . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 252 Soil depth . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 252 Drainage .................................................................................. 257 Soil fertility . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 259 Laterite . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 268 Soil types and vegetation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 270 IX. Distribution of cerrado vegetation over the landscape ......................... 275 X. Transitions to other vegetation provinces .. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 284 Transition to Amazonian forest ..................................................... 284 Transition to caatinga .................................................................. 288 Transition to Atlantic coastal forest ........................................... 288 Transition to southern Brazil grasslands .................................... 290 Transition to Chaco vegetation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 290 XI. The disjunct cerrados of northeastern Brazil . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 290 XII. Water relations and leaf xeromorphism .. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 295 XIII. Man's effect on the cerrado . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 303 Fire . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 303 Is cerrado a derived vegetation? . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 306 Grazing . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 317 Cultivation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 318 Cutting . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 318 Utilization . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 319 Cerrado and the savanna concept .. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 320 The cerrado as climax . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 321 Summary ................................................................................................ 3'26 Literature Cited .......................................................................................... 327 read more read less

Topics:

Vegetation (pathology) (73%)73% related to the paper, Plant ecology (57%)57% related to the paper
1,131 Citations
Journal Article DOI: 10.1007/BF02860857
Pattern, process, and natural disturbance in vegetation
Peter S. White1
07 Mar 1979 - Botanical Review

Abstract:

Natural disturbances have been traditionally defined in terms of major catastrophic events originating in the physical environment and, hence, have been regarded as exogenous agents of vegetation change. Problems with this view are: (1) there is a gradient from minor to major events rather than a uniquely definable set of maj... Natural disturbances have been traditionally defined in terms of major catastrophic events originating in the physical environment and, hence, have been regarded as exogenous agents of vegetation change. Problems with this view are: (1) there is a gradient from minor to major events rather than a uniquely definable set of major catastrophes for each kind of disturbance, and (2) some disturbances are initiated or promoted by the biotic component of the system. Floras are rich in disturbance-adapted species. Disturbances have probably exerted selective pressure in the evolution of species strategies. Heathland cyclic successions and gap-phase dynamics in forests have been viewed as endogenous patterns in vegetation. When death in older individividuals imposes a rhythm on community reproduction, dynamics may indeed be the result of endogenous factors. However, documented cases of senescence in perennial plants are few and many cyclic successions and cases of gap-phase dynamics are initiated by physical factors. Forest dynamics range from those that are the result of individual tree senescence and fall, through those that are the result of blowdown of small groups of healthy trees, to those that are the result of large windstorms which level hectares of forest. The effect of wind ranges from simple pruning of dead plant parts to widespread damage of living trees. Wind speed is probably inversely proportional to occurrence frequency. Disturbances vary continuously. There is a gradient from those community dynamics that are initiated by endogenous factors to those initiated by exogenous factors. Evolution has mediated between species and environment; disturbances are often caused by physical factors but the occurrence and outplay of disturbances may be a function of the state of the community as well. Natural disturbances in North American vegetation are: fire, windstorm, ice storm, ice push on shores, cryogenic soil movement, temperature fluctuation, precipitation variability, alluvial processes, coastal processes, dune movement, saltwater inundation, landslides, lava flows, karst processes, and biotic disturbances. Disturbances vary regionally and within one landscape as a function of topography and other site variables and are characterized by their frequency, predictability, and magnitude. The landscape level is important in assessing disturbance regime. Disturbances and cyclic successions belong to the same class of events—that of recurrent dynamics in vegetation structure—irrespective of cause. Dynamics may result from periodic, abrupt, and catastrophic environmental factors or they may result from an interaction of the changing susceptability of the community and some regular environmental factor. In any case, the dynamics result in heterogeneous landscapes; the species adapted to this heterogeneity are numerous, suggesting their long time importance. The importance of disturbance regime as part of the environmental context of vegetation means that allogenic and autogenic models of vegetation are difficult to apply. Species composition can be seen to be a function of disturbance regime, as well as other environmental variables. Competitive replacement in succession occurs, then, only as disturbances cease to operate and can be viewed as allogenic adjustment to a new disturbance-free environment. Competitive divergence, separation of role, and competition avoidance may, in fact, underlie successional patterns traditionally viewed as the competitive replacement of inferior species by superiorly adapted climax species. The importance of ongoing dynamics is also difficult to reconcile with the concept of climax, founded as it is on the idea of autogenesis within a stable physical environment. Climax composition is relative to disturbance regime. Climax is only arbitrarily distinguished from succession. Climax as an organizing paradigm in plant ecology has obscured the full temporal-spatial dimensions important in understanding the vegetated landscape and the evolution of species which contribute to the landscape patterns. Whittaker’s coenocline concept is accepted with modifications: (1) natural disturbance gradients and Whittaker’s complex gradient are intimately related, (2) temporal variation in the community should be viewed as an added axis of community pattern, and (3) ongoing dynamics have important effects on specificity of species to site relations and the predictability of vegetation patterns. Recent work has suggested an r-K continuum in species strategy. In general, colonizing ability is seen as a trade-off against specialization. Frequent disruption of the community and the creation of open sites seems to result in mixes of species that are fleeting in time and do not repeat in space. Species in such mixes are often tolerant of wide environmental extremes but are compressed into early successional time if disturbance ceases. The composition of such communities is not predictable from site characteristics. Even communities with low disturbance frequency lack complete environmental determinism, and historical events are important in understanding present composition. Communities vary in level of environmental determinism and species differ in niche breadth and degree of site specificity. Management implications of vegetation dynamics are discussed. read more read less

Topics:

Climax species (61%)61% related to the paper, Disturbance (ecology) (58%)58% related to the paper, Ecological succession (57%)57% related to the paper, Forest dynamics (55%)55% related to the paper, Vegetation (55%)55% related to the paper
1,035 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 The Botanical Review?

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 The Botanical Review. 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 The Botanical Review?

The 5 most common citation types in order of usage for The Botanical Review 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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