Hello community,
I have a silly question about betadisper() output interpretation. I am
using the function betadisper() after adonis to test for homogeneity of
variances. I have used it a lot in the years but I never get to look at the
boxplots output with the necessary attention.
Hello Luis,
I suggest you to try the vegan and BiodiversityR packages.
Best,
Gian
On Sat, 12 Dec 2020 at 02:03, Luis Fernando García
wrote:
> Dear all,
>
> I am wanting to compare the Eveness value in four localities. I found the
> sbdiv function in the simboot package which makes exactly
Hello sig-r-eco community,
I would love to have some insights on my interpretation of capscale() and
how to assess the variance explained by the interaction effect.
Imagine a model like this: Var1 + Var2 + Var1:Var2
> RsquareAdj(capscale(otu_table ~ Var1 + Var2 + Var1:Var2, metadata,
distance =
ot a statistician but software developer... hope that other members
> > of the mailing list are expert of distance matrices and can answer your
> > question.
> > Have a nice week,
> > Ákos
> >
> > 2019.06.03. 17:44 keltezéssel, Gian Maria Niccolò Benucci írta:
> &g
ecalculate
> the distance matrix (e.g. due to computer capacity or time), you can
> reorder the distance matrix (both the rows and columns).
> dist_b_reordered2 <- as.dist(as.matrix(dist_b)[attr(dist_a, "Labels"),
> attr(dist_a, "Labels")])
> all.equal(dist_
Hello,
I have two vegan::vegdist objects I want to use into a vegan::mantel test.
However, rows and columns of the two objects are not in the same order. Is
there a way to reorder them one another?
For example,
>dist_a
Lycovolu Hupeaust Lycofast Lycodeut
Hupeaust 0.9045557
Lycofast
) main
> effects and all these terms are marginal and can be removed, whereas the
> latter Stage*Growhouse expands to explicit main effects and interaction
> effects, and only the interaction effects are marginal and can be removed.
> This is also reflected in the degrees of freedom in
nly the interaction effects are marginal and can be removed.
> This is also reflected in the degrees of freedom in your anova table: In
> the first case Stage:Growhouse has 3 df, and in the latter only 1 df (and
> the main effects ignored had 2 df).
>
> Ciao, Giari
>
> > On 29 O
Hello Jari,
It is a little bit confusing. If A*B unfolds in A+B+A:B then A:B is the
real interaction component.
So, which if the code below will test the variance for the interaction
alone?
> adonis2(t(otu_fungi_out) ~ *Stage : Growhouse*, data=metadata_fungi_out,
by = "margin",
Hello dear ecologists,
I have a question for you in here. How important is to have a balanced
design for adonis? In other words, how sensitive is adonis() to differences
in sample numbers within the groups I am comparing?
To link this question to the reality, I am trying to compare the microbial
Hello all,
thank you for the interesting discussion on the topic. I have an additional
question that i thought would worth to ask directly here instead of opening
a new thread for it. How sensitive is adonis() to differences in sample
numbers of the groups I am comparing? To be more precise, I am
Good morning r-sig-ecologists,
I have a question for you on how to have a correct interpretation of
protest() output. I have read the R documentation where it is reported that
a correlation-like statistics is computed from the symmetric Procrustes sum
of squares also called squared m12 =
That's really good and useful, thank you for sharing!
G.
On 27 January 2017 at 06:11, Tania Bird wrote:
> Yes really an amazing resource!!
>
> Thank you so much for making it available.
>
> Tania
>
>
> On 27 Jan 2017 12:35, "Ralf Schäfer" wrote:
Hello everyone,
I am working on a fungal dataset with 151 OTUs distributed in 20 samples. I
have imported it as phyloseq object and as normal species matrix as well to
work with the vegan package.
I am trying to find a way to get relative abundances at different
hierarchical level goruping the
) function in the mefa4 package to get
your relative abundances.
Cheers,
Peter
Gian Maria Niccolò Benucci gian.benu...@gmail.com ezt írta (2015.
június 25., csütörtök):
Hello everyone,
I am working on a fungal dataset with 151 OTUs distributed in 20 samples.
I
have imported it as phyloseq object
need
to transpose or adjust the code I suggested before.
Peter
Gian Maria Niccolò Benucci gian.benu...@gmail.com ezt írta (2015.
június 25., csütörtök):
Hello,
thank you for the replies. My dataset is something like this:
datafungi
BR1 BR2 BR3 BR4 BR5 F1 F2 F3 F4
For SIMPER you can read this thread:
https://www.researchgate.net/post/What_do_you_think_about_Similarity_Percentage_analysis_SIMPER_to_measure_species_indicator_value
Moreover read the function help(simper) carefully, because: The results of
'simper' can be very difficult to interpret. The
Dear Martin and Mario,
thanks a lot, both of your code work greatly...
Now I have species that are common between two selected sites, but how to
to detect species that are unique between two selected sites? in other
words which species is present in the site A and which other in the site
B?
Dear Martin and dear all,
I tried your approach but I suppose it does not work...
my commands are the following, where's my mistake?
head(dune)
Belper Empnig Junbuf Junart Airpra Elepal Rumace Viclat Brarut Ranfla
Cirarv
2 3 0 0 0 0 0 0 0 0
0
Hi Martin,
thanks a lot. Also your commands are working... It's very nice to see how
different solutions in R can be found for a single problem.
I just have another question now, but... if I would know which species are
in common (and which not) between two particular selected samples?
Thanks for
Hi all R-sig-ecologists,
Sorry for the very simple and probably stupid question. I was wandering if
exist a simple method or a function in R, to detect which different species
are present among the samples of a given data community matrix.
Thanks a lot in advance,
--
Gian
wrote:
Hi Gian,
I don't understand what you're trying to do. Can you give a simple example
of your data and what your results should be?
Sarah
On Saturday, February 1, 2014, Gian Maria Niccolò Benucci
gian.benu...@gmail.com wrote:
Hi all R-sig-ecologists,
Sorry for the very simple
Hi,
Thank you very much for your help!
G.
On 19 July 2012 18:13, Gavin Simpson gavin.simp...@ucl.ac.uk wrote:
On Mon, 2012-06-25 at 16:46 +0200, Kay Cichini wrote:
Hi!
library(vegan)
data(dune)
sol - metaMDS(dune)
# use argument air! see ?orditorp:
plot(sol, type = n)
Hi community,
Very simple question. How to avoid overlap plot of species in a metaMDS()
diagram?
I used this command...
text(metaMDS_new2, display=c(species), cex=0.6)
but some species are plotted one over the other and is not simple to read
the diagram.
Thanks for helping,
--
Gian
Hallo ecologists,
I know that this is not the right place where to post my help-request so I
say sorry in advance. My question concern results of biodiversity indices
with diversityresult() tha I used to describe the diversity of two
different, comparable fungal communities.
This is what I got:
Dear Roman,
I have that book. But it is no mention on how the funtion calculate
diversity for different methods.
I assume someone used that function before, do anyone?
Thanks a lot!
Cheers,
--
Gian
2012/3/30 Roman Luštrik roman.lust...@gmail.com
If you know BiodiversityR, you probably
From: r-sig-ecology-boun...@r-project.org [
r-sig-ecology-boun...@r-project.org] on behalf of Gian Maria Niccolò
Benucci [gian.benu...@gmail.com]
Sent: 30 March 2012 11:57
To: r-sig-ecology@r-project.org
Subject: [R-sig-eco] diversityresult function - BiodiversityR package
Hi all
:
https://github.com/jarioksa/**vegan/issues/3https://github.com/jarioksa/vegan/issues/3
Let me know if your facing any problems with this function.
Cheers,
Edi
On 09/03/12 09:51, Gian Maria Niccolò Benucci wrote:
Hi members,
Do anyone know if SIMPER analysis (Clarke 1993) is implemented
Hi everyone,
I am doing a metaMDS in a sqrt() dataset of 24 samples. The NMDS diagram is
ok but when I try to see the Shepard diagram I have this result:
stressplot(metaMDS3)
Using step-across dissimilarities:
Too long or NA distances: 147 out of 276 (53.3%)
Stepping across 276
2012/2/23 Jari Oksanen jari.oksa...@oulu.fi
On 21/02/2012, at 13:38 PM, Gian Maria Niccolò Benucci wrote:
Dear All,
I just want to ask if someone can explane me how the steps are calculated
in taxa2dist().
I would know how steps are calculated because it is foundamental to
define
OTU30 OTU31 OTU32 UE1 UE2 UE3
UE4
[37] UE5 UE6
2012/2/16 Jari Oksanen jari.oksa...@oulu.fi
On 16/02/2012, at 18:39 PM, Gian Maria Niccolò Benucci wrote:
Hi everybody,
I am here for asking some kind of help about taxonimic diversity and
distinctness indices, from
taxondive
...@ucl.ac.uk
On Mon, 2012-02-20 at 16:28 +0100, Gian Maria Niccolò Benucci wrote:
Hi r-sig-ecology Members,
I would please you to examine the differences I found in metaMDS() and
nmds() outputs and possibly draw some conclusions. As I wrote in past
emails I have 24 samples of ectomycorrhizal
gavin.simp...@ucl.ac.uk
On Mon, 2012-02-20 at 17:24 +0100, Gian Maria Niccolò Benucci wrote:
Dear Gavin,
Thank you very much. I tried with your advice but the result is almost
unchanged...
Any further advice??
Yeah, what Sarah said. Read the documentation; the two functions use
different
only 15 points, instead of 24 that is the overall sample number,
becasue there is an overplotting...do is it possible?
Moreover, there is the possibility to plot in the funnel diagram the name
of the samples?
Thank you to everyone,
G.
--
Gian Maria Niccolò Benucci, Ph.D.
Department of Applied
2012/2/2 Gian Maria Niccolò Benucci gian.benu...@gmail.com:
...
Which among the 50 configuration the functions chose?
How to look to its stress and R2 values?
Forgot about the R-squared - according to the vegan FAQ 1 - stress^2
transforms nonlinear stress into quantity analogous to squared
() is that it lets you choose
a particular dimension solution rather than the lowest
available.
For your example, the same thing can be achieved with
iris.nmds$conf[[which.min(iris.nmds$stress)]]
Sarah
2012/2/2 Gian Maria Niccolò Benucci gian.benu...@gmail.com:
Hi all,
I am trying to run a nmds
of discussion and brainstorming, just let me
know how and if I can. I am a fungal eco-biologist (if the term is correct).
Cheers,
G.
--
Gian Maria Niccolò Benucci, Ph.D.
Department of Applied Biology
University of Perugia
Borgo XX Giugno, 74
06121 - Perugia, ITALY
Tel: +390755856433
Email: gian.benu
very much,
G.
2012/2/2 Jari Oksanen jari.oksa...@oulu.fi
On 02/02/2012, at 19:43 PM, Gian Maria Niccolò Benucci wrote:
Hi Members,
I tried to use a metaMDS to explore my two fungal communities data.
That's the result:
Call:
metaMDS(comm = species.data_log, distance = bray, k
be tested.
G
gabriel
On 11/16/11 11:02 PM, Gavin Simpson wrote:
On Wed, 2011-11-16 at 03:43 +0100, Gian Maria Niccolò Benucci wrote:
Hi all,
I had 84 samples collected in 7 different sites.
In each sample were individuated the different fungal species and
recorded.
I would test
-11-16 at 03:43 +0100, Gian Maria Niccolò Benucci wrote:
Hi all,
I had 84 samples collected in 7 different sites.
In each sample were individuated the different fungal species and
recorded.
I would test if exist a real difference between the sites and if exist a
sort of site effect
Hi all,
I had 84 samples collected in 7 different sites.
In each sample were individuated the different fungal species and recorded.
I would test if exist a real difference between the sites and if exist a
sort of site effect that structure the fungal communities...
Then, I did adonis test
Dear Manuel,
I did it with vegan function *diversityresult().* Look to R help for this
function there are many parameters you can modify and add to it.
The code is:
library(vegan)
diversityresult(X, index=richness)
I hope it helps,
Gian
--
Gian Maria Niccolò Benucci
Ph.D. Candidate
Hi everybody,
I have plotted a diana dendrogram. The names of samples under the dendrogram
lines are unfortunately too big. How do I reduce samples name down into the
dendrogram plot?
Every advice is greatly welcome, thank you in advance!
--
Gian
[[alternative HTML version deleted]]
Thank you a lot for your aid...
Cheers,
Gian
On 14 December 2010 13:21, Wade Wall wade.w...@gmail.com wrote:
Gian,
I have found Analysis of Ecological Communities by McCune and Grace to be
a really good resource for understanding NMDS and other multivariate
techniques. It has
Hi everybody,
I was wondering if exist something where to read about NMS outputs. In
particular about commenting a generated NMS ordination graph.
Thank you very very much in advance,
Gian
[[alternative HTML version deleted]]
___
, for a
univariate ANOVA test.
When including the results in a paper or dissertation, it would be
normal to quote both values (R and significance).
I hope that's helpful,
Barbara
- Original Message -
From: Gian Maria Niccolò Benucci gian.benu...@gmail.com
Date: Tuesday, June 8, 2010 4:57 am
software, is it true? Because I try to find the correct
function fot that but I didn't find it already.
Thanks a lot in advance to Jari who surely concern with my question, and to
all will help me in that.
G.
--
Gian Maria Niccolò Benucci
Ph.D. Candidate
Department of Applied Biology - University
0034 956832612 ext. 316
~*~*~*~*~*~*~*~*~*~*~*~*~*~*~*~*~*~*~*~*~*~*~*~*
Gian Maria Niccolò Benucci escribió:
Barbara,
Thank you very much, indeed I red the two values on a paper, that were of
R=0.15 and P=0.006, and they states that the difference between the two
groups
Hi,
Thanks a lot, I've found the functions: vegdist and designdist.
Cheers,
G.
On Wed, Jun 9, 2010 at 11:26 AM, romunov romu...@gmail.com wrote:
?vegdist
On Wed, Jun 9, 2010 at 11:21 AM, Gian Maria Niccolò Benucci
gian.benu...@gmail.com wrote:
Hi all again,
I have red
to propose to people
just starting with statistics and I still use it when I need a quick
overview on my analyses): http://folk.uio.no/ohammer/past/
Cheers
Angélique
Gian Maria Niccolò Benucci wrote:
Hi Angélique,
Many many thanks about your help, I will read the paper carefully. It's
always
-- Forwarded message --
From: Gian Maria Niccolò Benucci gian.benu...@gmail.com
Date: 2010/5/22
Subject: Re: [R-sig-eco] Graphical parameters in metaMDS
To: Jari Oksanen jari.oksa...@oulu.fi
Jari,
Sorry, in the future I will spcify the pakages where the functions
will be surely appreciated, many thank you in advance...
Gian
--
Gian Maria Niccolò Benucci
Ph.D. Candidate
Department of Applied Biology - University of Perugia
Borgo XX Giugno, 74
I-06121 - Perugia, ITALY
Tel: +39.0755856433
Fax: +39.0755856069
Email: gian.benu...@gmail.com
[[alternative HTML
*random* effects in adonis(), which was intended as the main message of my
previous posting on this issue. They are all fixed effects.
Cheers, Jari Oksanen
--
Dr. Gian Maria Niccolò Benucci
Department of Applied Biology - University of Perugia
Borgo XX Giugno, 74
I-06121 - Perugia, ITALY
on that...
Cheers,
Gian
--
Dr. Gian Maria Niccolò Benucci
Department of Applied Biology - University of Perugia
Borgo XX Giugno, 74
I-06121 - Perugia, ITALY
Email: gian.benu...@gmail.com
Tel: +39.075.5856433
2009/12/10 Maria Dulce Subida mdsub...@icman.csic.es
Dear Gian,
I'm still not quite sure
%~%~%~%~%~%~%~%~%~%~%~%~%~%~%~%~%~%~%~%~%~%~%~%~%~%~%~%~%~%~%~%~%~%~%
--
Dr. Gian Maria Niccolò Benucci
Department of Applied Biology - University of Perugia
Borgo XX Giugno, 74
I-06121 - Perugia, ITALY
Email: gian.benu...@gmail.com
Tel: +39.075.5856433
[[alternative HTML version deleted
Hi all again,
And thank you all for the kind responses...
I do not want to torture myself for sure... :) I red (lot of) publications
about fungal community ecology studies (soil fungi), my research field
indeed, and all uses NMDS or DCA as ordination techniques... So, I am only
trying to do my
Jari,
I am here again ... :)
So, to try having a comparison of the real goodness of my metaMDS data I
tried to perform a DCA (with same input table)
Then please forgive me if I do somethign wrong with it... That's my R code:
decorana(sqrtABCD, iweigh=0, ira=0) - DCA.1
DCA.1
Call:
decorana(veg
I am here again ... :)
So, to try having a comparison of the real goodness of my metaMDS data I
tried to perform a DCA (with same input table)
Then please forgive me if I do somethign wrong with it... That's my R code:
decorana(sqrtABCD, iweigh=0, ira=0) - DCA.1
DCA.1
Call:
decorana(veg =
Okey, I understood...
I have a matrix of 40 rows (samples) and 29 columns (species). In the
ordination graph the data divide in two clades ( as i supposed they must
to)... and that's my best solution for reduce the Stress...
metaMDS(sqrtABCD, distance = bray, k = 23, trymax = 50, autotransform
Jari,
Yes, you right, I am sorry I didn't say that I was talking about Euclidean
measure of distance in that passage, I know that other distance are
different, and finally I understood the non-linear regression stuff, now is
much more clear!
If you have some good book titles I would appreciate a
Hi Hi there,
I am trying to use funcion metaMDS (vegan pakage) for Community Ecology
data, but I find no way to calculate the expressed variance of the first 2
axis? is there a way to do that?
Thanks a lot in advance,
Gian
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