Example of Helgoland Marine Research format
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Example of Helgoland Marine Research format Example of Helgoland Marine Research format Example of Helgoland Marine Research format Example of Helgoland Marine Research format Example of Helgoland Marine Research format Example of Helgoland Marine Research format Example of Helgoland Marine Research format Example of Helgoland Marine Research format Example of Helgoland Marine Research format Example of Helgoland Marine Research format Example of Helgoland Marine Research format Example of Helgoland Marine Research format Example of Helgoland Marine Research format Example of Helgoland Marine Research format Example of Helgoland Marine Research format Example of Helgoland Marine Research format Example of Helgoland Marine Research format Example of Helgoland Marine Research format
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Example of Helgoland Marine Research format Example of Helgoland Marine Research format Example of Helgoland Marine Research format Example of Helgoland Marine Research format Example of Helgoland Marine Research format Example of Helgoland Marine Research format Example of Helgoland Marine Research format Example of Helgoland Marine Research format Example of Helgoland Marine Research format Example of Helgoland Marine Research format Example of Helgoland Marine Research format Example of Helgoland Marine Research format Example of Helgoland Marine Research format Example of Helgoland Marine Research format Example of Helgoland Marine Research format Example of Helgoland Marine Research format Example of Helgoland Marine Research format Example of Helgoland Marine Research format
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open access Open Access

Helgoland Marine Research — Template for authors

Publisher: Springer
Categories Rank Trend in last 3 yrs
Aquatic Science #72 of 224 down down by 1 rank
Oceanography #46 of 128 down down by 5 ranks
journal-quality-icon Journal quality:
Good
calendar-icon Last 4 years overview: 76 Published Papers | 266 Citations
indexed-in-icon Indexed in: Scopus
last-updated-icon Last updated: 02/06/2020
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Related Journals

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open access Open Access

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Quality:  
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CiteRatio: 4.6
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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.

1.25

3% from 2018

Impact factor for Helgoland Marine Research from 2016 - 2019
Year Value
2019 1.25
2018 1.208
2017 0.949
2016 1.013
graph view Graph view
table view Table view

3.5

46% from 2019

CiteRatio for Helgoland Marine Research from 2016 - 2020
Year Value
2020 3.5
2019 2.4
2018 2.6
2017 3.0
2016 3.6
graph view Graph view
table view Table view

insights Insights

  • Impact factor of this journal has increased by 3% in last year.
  • This journal’s impact factor is in the top 10 percentile category.

insights Insights

  • CiteRatio of this journal has increased by 46% 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.

0.634

33% from 2019

SJR for Helgoland Marine Research from 2016 - 2020
Year Value
2020 0.634
2019 0.477
2018 0.623
2017 0.599
2016 0.632
graph view Graph view
table view Table view

1.058

34% from 2019

SNIP for Helgoland Marine Research from 2016 - 2020
Year Value
2020 1.058
2019 0.788
2018 0.748
2017 0.664
2016 0.767
graph view Graph view
table view Table view

insights Insights

  • SJR of this journal has increased by 33% in last years.
  • This journal’s SJR is in the top 10 percentile category.

insights Insights

  • SNIP of this journal has increased by 34% in last years.
  • This journal’s SNIP is in the top 10 percentile category.

Helgoland Marine Research

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Springer

Helgoland Marine Research

The journal publishes original research papers, invited reviews, and comments on any aspect and level of the biology of marine and brackish water organisms. Topics of particular interest are: - Ecological dynamics - Life cycles - Biological oceanography - Environmental biology...... Read More

Oceanography

Aquatic Science

Earth and Planetary Sciences

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Last updated on
02 Jun 2020
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ISSN
1606-8610
i
Impact Factor
Medium - 0.943
i
Open Access
No
i
Sherpa RoMEO Archiving Policy
White faq
i
Plagiarism Check
Available via Turnitin
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Endnote Style
Download Available
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Bibliography Name
SPBASIC
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Citation Type
Numbered
[25]
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Bibliography Example
Blonder, G.E., Tinkham, M., Klapwijk, T.M.: Transition from metallic to tunneling regimes in superconducting microconstrictions: Excess current, charge imbalance, and supercurrent conversion. Phys. Rev. B 25(7), 4515–4532 (1982)

Top papers written in this journal

open accessOpen access Journal Article DOI: 10.1007/BF02367105
TBT-induced imposex in marine neogastropods is mediated by an increasing androgen level
C. Bettin1, Jörg Oehlmann, E. Stroben1

Abstract:

Tributyltin (TBT) exposure at different concentrations (5, 60, and 100 ng TBT as Sn/l) induces a concentration- and time-dependent imposex (=pseudohermaphroditism) development in femaleNucella lapillus andHinia reticulata. In both species the average imposex stage, termed as vas deferens sequence (VDS) index, and the average ... Tributyltin (TBT) exposure at different concentrations (5, 60, and 100 ng TBT as Sn/l) induces a concentration- and time-dependent imposex (=pseudohermaphroditism) development in femaleNucella lapillus andHinia reticulata. In both species the average imposex stage, termed as vas deferens sequence (VDS) index, and the average female penis length increases with increasing TBT concentration and duration of TBT exposure. Testosterone added at a concentration of 500 ng/l induces a faster and more intensive imposex development compared to that induced by the TBT concentrations used in the present experiments. Radioimmunological determination of endogenous steroid content reveals increasing testosterone titres in female gastropods exposed to TBT which correlate with the TBT concentration used and the duration of the experiment. The most marked and highest increase of the endogenous testosterone level is exhibited by females, of both species exposed to testosterone. Simulataneous exposure to TBT and to the antiandrogen cyproterone acetate which suppresses imposex development completely inN. lapillus and reduces imposex development strongly inH. reticulata proves that the imposex-inducing effects of TBT are mediated by an increasing androgen level and are not caused directly by the organotin compound itself. Further-more, TBT-induced imposex development can be suppressed in both snails by adding estrogens to the aqueous medium. These observations suggest that TBT causes an inhibition of the cytochrome P-450 dependent aromatase system which catalyses the aromatization of androgens to estrogens. The increase of the androgen content or the shift of the androgen-estrogen balance in favour of androgens induces the development of pseudohermaphroditism in marine prosobranchs. Artificial inhibition of the cytochrome P-450 dependent aromatase system using SH 489 (1-methyl-1,4-androstadiene-3,17-dione) as a steroidal aromatase inhibitor and flavone as a nonsteroidal aromatase inhibitor induces imposex development inN. lapillus as well as inH. reticulata. read more read less

Topics:

Imposex (58%)58% related to the paper, Tributyltin (54%)54% related to the paper
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338 Citations
open accessOpen access Journal Article DOI: 10.1007/S10152-004-0196-0
The warming trend at Helgoland Roads, North Sea: phytoplankton response
Karen Helen Wiltshire1, Bryan F. J. Manly

Abstract:

We combine the temperature and phytoplankton data from one of the longest aquatic data sets in history, the Helgoland Roads (North Sea, 54°11.3’N, 7°54.0’E) timeseries to evaluate the effects of climate change on the base of marine food webs. The data shows that, despite an obvious warming of 1.1°C since 1962, the mean diatom... We combine the temperature and phytoplankton data from one of the longest aquatic data sets in history, the Helgoland Roads (North Sea, 54°11.3’N, 7°54.0’E) timeseries to evaluate the effects of climate change on the base of marine food webs. The data shows that, despite an obvious warming of 1.1°C since 1962, the mean diatom day of the algal spring bloom is delayed and shifted to the end of the first quarter of the year. This is apparently related to a warming of the autumn (October–December) temperatures. It is the first indication of a warming related shift in phytoplankton succession, the consequences of which would range from lifecycle/food resource mismatches to regime shifts in the North Sea system. read more read less

Topics:

Spring bloom (60%)60% related to the paper, Global warming (55%)55% related to the paper, Phytoplankton (54%)54% related to the paper
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299 Citations
open accessOpen access Journal Article DOI: 10.1007/BF02366043
Relative importance of temperature and other factors in determining geographic boundaries of seaweeds: Experimental and phenological evidence
A. M. Breeman1

Abstract:

Experimentally determined ranges of thermal tolerance and requirements for completion of the life history of some 60 seaweed species from the North Atlantic Ocean were compared with annual temperature regimes at their geographic boundaries. In all but a few species, thermal responses accounted for the location of boundaries. ... Experimentally determined ranges of thermal tolerance and requirements for completion of the life history of some 60 seaweed species from the North Atlantic Ocean were compared with annual temperature regimes at their geographic boundaries. In all but a few species, thermal responses accounted for the location of boundaries. Distribution was restricted by: (a) lethal effects of high or low temperatures preventing survival of the hardiest life history stage (often microthalli), (b) temperature requirements for completion of the life history operating on any one process (i.e. [sexual] reproduction, formation of macrothalli or blades), (c) temperature requirements for the increase of population size (through growth or the formation of asexual propagules). Optimum growth/reproduction temperatures or lethal limits of the non-hardiest stage (often macrothalli) were irrelevant in explaining distribution. In some species, ecotypic differentiation in thermal responses over the distribution range influenced the location of geographic boundaries, but in many other species no such ecotypic differences were evident. Specific daylength requirements affected the location of boundaries only when interacting with temperature. The following types of thermal responses could be recognised, resulting in characteristic distribution patterns: (A) Species endemic to the (warm) temperate eastern Atlantic had narrow survival ranges (between ca 5 and ca 25°C) preventing occurrence in NE America. In species with isomorphic life histories without very specific temperature requirements for reproduction, northern and southern boundaries in Eur/Africa are set by lethal limits. Species with heteromorphic life histories often required high and/or low temperatures to induce reproduction in one or both life history phases which further restricted distribution. (B) Species endemic to the tropical western Atlantic also had narrow survival ranges (between ca 10 and ca 35°C). Northern boundaries are set by low, lethal winter temperatures. Thermal properties would potentially allow occurrence in the (sub) tropical eastern Atlantic, but the ocean must have formed a barrier to dispersal. No experimental evidence is so far available for tropical species with an amphi-Atlantic distribution. (C) Tropical to temperate species endemic to the western Atlantic had broad survival ranges (<0 to ca 35°C). Northern boundaries are set by low summer temperatures preventing (growth and) reproduction. Thermal properties would permit occurrence in the (sub)tropical eastern Atlantic, but along potential “stepping stones” for dispersal in the northern Atlantic (Greenland, Iceland, NW Europe) summer temperatures would be too low for growth. (D) In most amphi-Atlantic (tropical-) temperate species, northern boundaries are set by low summer temperatures preventing reproduction or the increase of population size. On European shores, species generally extended into regions with slightly lower summer temperatures than in America, probably because milder winters allow survival of a larger part of the population. (E) Amphi-Atlantic (Arctic-) temperate species survived at subzero temperatures. In species with isomorphic life histories not specifically requiring low temperatures for reproduction, southern boundaries are set by lethally high summer temperatures on both sides of the Atlantic. None of the species survived temperatures over 30°C which prevents tropical occurrence. Species with these thermal responses are characterized by distribution patterns in which southern boundaries in Eur/Africa lie further south than those in eastern N America because of cooler summers. In most species with heteromorphic life histories (or crustose and erect growth forms), low temperatures were required for formation of the macrothalli (either directly or through the induction of sexual reproduction). These species have composite southern boundaries in the north Atlantic Ocean. On American coasts, boundaries are set by lethally high summer temperatures, on European coasts by winter temperatures too high for the induction of macrothalli. Species with this type of thermal responses are characterized by distribution patterns in which the boundaries in Eur/Africa lie further north than those in eastern N America because of warmer winters. read more read less

Topics:

Population (54%)54% related to the paper, Biological dispersal (52%)52% related to the paper, Temperate climate (52%)52% related to the paper, Range (biology) (51%)51% related to the paper
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268 Citations
open accessOpen access Journal Article DOI: 10.1007/S10152-004-0195-1
Introduced Pacific oysters (Crassostrea gigas) in the northern Wadden Sea: Invasion accelerated by warm summers?
Susanne Diederich1, Georg Nehls, J. E. E. van Beusekom1, Karsten Reise1

Abstract:

Among the increasing number of species introduced to coastal regions by man, only a few are able to establish themselves and spread in their new environments. We will show that the Pacific oyster (Crassostrea gigas) took 17 years before a large population of several million oysters became established on natural mussel beds in... Among the increasing number of species introduced to coastal regions by man, only a few are able to establish themselves and spread in their new environments. We will show that the Pacific oyster (Crassostrea gigas) took 17 years before a large population of several million oysters became established on natural mussel beds in the vicinity of an oyster farm near the island of Sylt (northern Wadden Sea, eastern North Sea). The first oyster, which had dispersed as a larva and settled on a mussel bed, was discovered 5 years after oyster farming had commenced. Data on abundance and size-frequency distribution of oysters on intertidal mussel beds around the island indicate that recruitment was patchy and occurred only in 6 out of 18 years. Significant proportions of these cohorts survived for at least 5 years. The population slowly expanded its range from intertidal to subtidal locations as well as from Sylt north- and southwards along the coastline. Abundances of more than 300 oysters m−2 on mussel beds were observed in 2003, only after two consecutive spatfalls in 2001 and 2002. Analyses of mean monthly water temperatures indicate that recruitment coincided with above-average temperatures in July and August when spawning and planktonic dispersal occurs. We conclude that the further invasion of C. gigas in the northern Wadden Sea will depend on high late-summer water temperatures. read more read less

Topics:

Oyster farming (64%)64% related to the paper, Pacific oyster (62%)62% related to the paper, Oyster (61%)61% related to the paper, Crassostrea (58%)58% related to the paper, Intertidal zone (52%)52% related to the paper
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242 Citations
open accessOpen access Journal Article DOI: 10.1007/BF02207862
Organisation in the pelagic ecosystem
Trevor Platt1, Kenneth L. Denman1

Abstract:

A continuous, steady-state theory has been developed for the abundance of organisms in the pelagic ecosystem as a function of their body weight. It is based on accepted relationships for the weight-dependence of metabolism and growth, in a context where individual organisms are assigned to one of a series of size classes for ... A continuous, steady-state theory has been developed for the abundance of organisms in the pelagic ecosystem as a function of their body weight. It is based on accepted relationships for the weight-dependence of metabolism and growth, in a context where individual organisms are assigned to one of a series of size classes for which the nominal weights increase in a geometric progression. Analysis of the biomass flow in such a representation leads to the conclusion that, in the steady state, the total biomass in any given size class decreases in a regular manner with increasing size. Explicitly,b(w 2)/b(w 1)~(w 2/w 1)0.22, whereb(w 2) andb(w 1) are the total biomasses in the size classes characterised by weightsw 2 andw 1, respectively. The exponent (−0.22) represents a balance between catabolism and anabolism, based on published reviews concerning the revelant parameters. This result agrees favourably with data collected by other workers in the subtropical oceans. The theory can be used to draw conclusions about the functional dynamics of the pelagic ecosystem, such as community respiration and rate of biomass flow. read more read less
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236 Citations
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Helgoland Marine Research format uses SPBASIC citation style.

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Frequently asked questions

1. Can I write Helgoland Marine Research in LaTeX?

Absolutely not! Our tool has been designed to help you focus on writing. You can write your entire paper as per the Helgoland Marine Research guidelines and auto format it.

2. Do you follow the Helgoland Marine Research guidelines?

Yes, the template is compliant with the Helgoland Marine Research guidelines. Our experts at SciSpace ensure that. If there are any changes to the journal's guidelines, we'll change our algorithm accordingly.

3. Can I cite my article in multiple styles in Helgoland Marine Research?

Of course! We support all the top citation styles, such as APA style, MLA style, Vancouver style, Harvard style, and Chicago style. For example, when you write your paper and hit autoformat, our system will automatically update your article as per the Helgoland Marine Research citation style.

4. Can I use the Helgoland Marine Research templates for free?

Sign up for our free trial, and you'll be able to use all our features for seven days. You'll see how helpful they are and how inexpensive they are compared to other options, Especially for Helgoland Marine Research.

5. Can I use a manuscript in Helgoland Marine Research that I have written in MS Word?

Yes. You can choose the right template, copy-paste the contents from the word document, and click on auto-format. Once you're done, you'll have a publish-ready paper Helgoland Marine Research that you can download at the end.

6. How long does it usually take you to format my papers in Helgoland Marine Research?

It only takes a matter of seconds to edit your manuscript. Besides that, our intuitive editor saves you from writing and formatting it in Helgoland Marine Research.

7. Where can I find the template for the Helgoland Marine Research?

It is possible to find the Word template for any journal on Google. However, why use a template when you can write your entire manuscript on SciSpace , auto format it as per Helgoland Marine Research's guidelines and download the same in Word, PDF and LaTeX formats? Give us a try!.

8. Can I reformat my paper to fit the Helgoland Marine Research's guidelines?

Of course! You can do this using our intuitive editor. It's very easy. If you need help, our support team is always ready to assist you.

9. Helgoland Marine Research an online tool or is there a desktop version?

SciSpace's Helgoland Marine Research is currently available as an online tool. We're developing a desktop version, too. You can request (or upvote) any features that you think would be helpful for you and other researchers in the "feature request" section of your account once you've signed up with us.

10. I cannot find my template in your gallery. Can you create it for me like Helgoland Marine Research?

Sure. You can request any template and we'll have it setup within a few days. You can find the request box in Journal Gallery on the right side bar under the heading, "Couldn't find the format you were looking for like Helgoland Marine Research?”

11. What is the output that I would get after using Helgoland Marine Research?

After writing your paper autoformatting in Helgoland Marine Research, you can download it in multiple formats, viz., PDF, Docx, and LaTeX.

12. Is Helgoland Marine Research's impact factor high enough that I should try publishing my article there?

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 Helgoland Marine Research?

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 Helgoland Marine Research. 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 Helgoland Marine Research?

The 5 most common citation types in order of usage for Helgoland Marine Research are:.

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

15. How do I submit my article to the Helgoland Marine Research?

It is possible to find the Word template for any journal on Google. However, why use a template when you can write your entire manuscript on SciSpace , auto format it as per Helgoland Marine Research's guidelines and download the same in Word, PDF and LaTeX formats? Give us a try!.

16. Can I download Helgoland Marine Research in Endnote format?

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 Helgoland Marine Research Endnote style according to Elsevier guidelines.

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