Questions related to CCA
Hi! My group and I are working on our undergraduate thesis about comparative study of intertidal gastropods in protected and unprotected areas. We measured the physicochemical parameters (temperature, pH, salinity, electrical conductivity, dissolved oxygen, and substrate type) in three replicates per area during sampling. Our MANOVA showed significant difference between the two areas based on the physicochemical parameters, except for temperature.
We collected 782 individual gastropods from the unprotected area and 665 individuals from the protected area. Only a few species were present in both areas.
Our CCA resulted in an Eigenvalue of 0.766 and a p-value of 1, using N = 999.
We also used One-way ANOSIM with a Bray-Curtis matrix: N = 9999; mean rank within = 2; mean rank between = 4.25; R = 0.75; p = 0.3348.
My question is: Is our data still biologically meaningful even if the p-values are > 0.05? Should we still use CCA and ANOSIM, or would you suggest more appropriate statistical analysis tools?
Thank you very much!
5' GGGGACGAAATTGGTTTCGACTGTTGTTGCCAGGGGTTATGTGGCGTGTAGAGGTTGTAGGCTCCTCTAAAAACCTTCAAACAATAACCGCTAATAACGAATTAGCTTTAGCAGCTTAATCTCTGCTACGGAACTTTAGTTTTTTCTCTCGAATTCTAAATGTTCTGACAATGATCGGGAGGCGATTCTTTTGGTTTTTGGTTCCTAAAAGAGTTTGTATTTGAGCCGAATAGGAAAGAGAGTCCTGTCTGAGGGTGAACCTCTTTCCGAAATTTTATACACAGACTACACACGTAGAGGCTGATCTGGGGCGCAATAGGACGCGGGTTCGAACCCCGCCGTCTCCAA 3' - I have this gene cloned in pTZ57R/T plasmid between the sites HindIII (forward) and KpnI (reverse). But I am unable to figure out how do I design a primer that the gene it ends with 3' CCA? Or more specifically if I want to cut and linearize the plasmid I want 3' to end with CCA. So what enzyme shall I use? Because even if I do a mutation and make sure 3' ends with CCA, how will I linearize it then?
My goal is to improvise and validate an instrument assessing various 3actors. Since my study involves new concepts that have little studies done previously therefore lack similar empirical data to confirm the hypothesis formed in the study. My question is, CCA involves several steps and the last step calls for nomological validity and predictive validity. How is it possible those out? Can it be left out?
Dear colleagues, i want to know or understand how to present CCA results and interpret them. i also want to know if there is any statistical software that can help. Please add readable materials. Thank you.
If the answer of the above question is negative, could you please recomend an analysis for that?
Thank you in advance!
Przemyslaw
I am trying to run an RDA or CCA (Redundancy Analysis, And Canonical Correlation) to illustrate the relationship between measured gene abundance and a set of env. variables. The environmental variables are measured in greatly different scales (pH, oxygen concentration, Nitrogen concentration, Temperature....). I realized that I need to standarise my data after getting some strange results in the RDA. I was wondering if I could use excel to calculate a z-score (for each variable) by just grabbing all the data for each variable and follwing the normal procedure. Then I would use those z-scores for RDA directly. Could I do that for all env. variables at once? As I understand it, I dont need to standarize my gene abundance data (response variables) since its all on the same scale.
I heard about CANOCO but it isn´t free.
Good morning researchers! Pls Sir/Madam, help me to have a research journals related to PCA and CCA regards to water quality, fish species diversity, assemblage or composition and aquatic plants
Hi guys,
I have raised a question regarding selecting proper statistical methods for the temporal analysis of community composition data. My study site is a river, and it has been implemented with a fishing ban a few years ago. On the other hand, by monitoring water quality parameters, we found the river has also benefited from slightly improved water quality in recent years.
After a long-term fish survey, we found significant changes in fish communities before and after the fishing ban (with one-way PERMANOVA analysis). However, we are not sure what is the main driver for the changes, the fishing ban or improved water quality.
I know that canonical correspondence analysis (RDA/CCA) has been widely used to determine the relationships between biological communities and associated environmental factors. I'm wondering if it's reasonable to consider time series as an environmental factor, by splitting sampling date into before and after, and using it in the CCA analysis with other water quality parameters (please find attached the figure for explanation). However, I didn't find an example for this, which makes me wonder if it's not correct.
Or if there are better statistical method that commonly used in ecology studies to slove this query?
Many thanks!
Rui

Actually, I am using this software for the analysis of different orders of insect with seven different soil parameters and want to draw a biplot graph to use CCA in PAST, and I am not sure if I am putting my variable correctly or not???
Need help in this regard?
I have two type of datasets, the first : numbers of species 2- the environmental variables of the sampling.
I am wondering if CCA (canonical correspondence analysis) is still considered valid and used with these datasets or should I follow another analysis (RDA)?
Coherence and correlation seem very similar to each other to me; while, coherence assesses similarity of the signals in frequency space rather than time space. I was wondering whether it is possible to employ coherence instead of correlation in Canonical Correlation Analysis.
I have to justify why I am not going to transform abundance vegetation data. I am using a CCA to study succession of a particular ecosystem. I get more interpretable results with non-transformation of my data. I would appreciate any scientific references why is not necessary to transform those data. Thanks a lot!
i am analysing the associations between social sustainability practices (62 observed indicators) that are grouped under 8 social categories, and sustainability enablers (10 observed indicators)
it is theoretically hypothesised that there is positive correlation between social sustainability practices and the enablers.
i'am interested in knowing the observed indicators and drawing conclusion based on that, i do not want to draw conclusions based on constructs.
can i use canonical correlation analysis (CCA) to analyse the strength of associations between 62 social indicator (dependent set) and another set of the 10 enablers ( independent set)?
or is it better to use structural equation modelling (SEM) and analyse path coefficients from independent variable (enablers) ----------------> 8 social categories each forming a latent dependent variable?
Dear Researchers!
I calculated the values of CCA, with 7 environmenta variables (independent) and 15 species (dependet variables), three different sites. The results are there in graphical form. Can anyone help me interpretate these results?
Please help!

Dear experts,
I am very new in the field of ecology and now dealing with a dataset (including community data (zero-inflated) and 10 environmental variables), with a two-level factor. I have subjected the community data to the calculation of the dissimilarity matrix (Bray-Curtis) and visualized dissimilarities using NMDS. Also, I have applied ANOSIM and confirmed the significant difference between the two groups of sites.
I want to further examine how the environmental variables affect the dissimilarities in the composition of communities. I have read some papers and found that several methods were used with the same type of data (many use CCA and others used db-RDA), both give similar visualization and coefficient.
Could you give me advice to chose the suitable one for my data?
Thanks in advance,
Linh Ha
Hi there,
I am planning to correlate microbial community with environmental variables using CCA. Is there any minimum for data replication? How many times should I go for sampling to per site ( assuming I have 5 sites ) to allow CCA? or would one time sampling be sufficient?
Thank you
Greetings,
According to Hair et al. (2020) about the Confirmatory Composite Analysis (CCA) to assess quality of the measurement model, Nomological and Predictive validity steps are suggested. would someone explain how can i apply these in Smart-PLS software and what exactly the indices or measures that i should extract?
thank you in advance.
I analyze my ecological data using Canonical Correspondence Analysis (CCA) and I am a little bit confused with the eigenvalue function in ecological interpretation, is there an eigenvalue function in ecological data interpretation, or it is just statistical?
Hi everyone,
I have longitudinal data for the same set of 300 subjects over seven years. Can I use '''year' as a control variable? Initially, I used one way ANOVA and found no significant different across seven years in each construct.
Which approach is more appropriate?. Pooling time series after ANOVA (if not significant) or using 'year' as a control variable?
Carpomyia vesuviana Costa is monophagous, destructive pests, and endogenous species infesting on Zizyphus spp.
I have tried many primers with gradient PCR for their molecular identification but they and not working properly.
Primers Names
X-F: 5′-ACG ATG ATG CGA TTG GTG AC-3 ′
X-R: 5′-TAT TGG TCG CGG AAC AAA CC-3 ′
COI CLepFolF 5'---ATT CAA CCA ATC ATAAAG ATA TTG G
CLepFolR 5'--TAA ACT TCT GGA TGT CCA AAA AAT CA
LCO1490 and HCO2198
Kindly provide your valuable inputs and suggestions regarding the procedure and usage of CCA in PLS-SEM. Please do suggest some links, videos, and references for the same. Any kind of help will be highly appreciated.
I need it for my understanding of the phenomenon of PLS-SEM (CCA)
Hello all, I'm looking for a adaptable interpretation for my data. It contains environmental factors and phylum abundance for 8 samples. I read that the CCA (canonical correspondence analysis) is a good choice to interpret the relationship between two groups of variables.
But the question is, after apply the test in R (anova.cca(phylum_cca, permutations = 999)), the model returns a Pr>F and equals 0.133. Besides, for overview the test for axis, the code doesn't work (anova.cca(phylum_cca, by = 'axis', permutations = 999), it gives the answer "model must be fitted with formula interface". I wonder it could be due to the p-value of my model > 0.05.
So what could I do in this situation? Should I ignore the significance and continue using CCA as the method? Or if there's other appropriate method that I can apply to my data?
Thanks so much!
I am working on developing a scale. I am through with EFA and in the field to gather data for assessing the structural fit.
How do I connect the dimensions of the model on a SmartPLS Canvas? Since there is no dependent variable in the model. Where should the connecting arrows go? From one construct of the proposed scale to the other?
If we want to study arthropod abundance and diversity on various managements/landscapes, we also record the temperature, RH, precipitation, or sometimes specifically, we measure soil properties, host plant's phytochemical components or landscape characteristics.
I read the book authored by Alain Zuur et al. (Mixed Effects Models and Extension in Ecology with R), but I could not understand the book well because of my inadequate knowledge of statistics. Because many studies used different approaches, I don't know when we should use PCA, CCA, GLM, or LME, or their variation.
If I record arthropod abundance and diversity on various landscapes (identified at least to family level), and I measure the physical environmental properties,
What is the best analysis that could describe the effects of the environmental factors on the arthropod abundance and diversity?
To date, I only use Pearson's correlation to determine the relationship between the observed variables with the environmental factors. But I know that the correlation analysis cannot give robust results or the analysis results could be overestimated. Even in my own experience, if there is no significant correlation, I'll just remove one of the variables/factors.
Thank you.
I have conducted regularized canonical correlation analysis using MixOmics package in R studio because the number of variables in my data are more than that number of observations. I now want conduct commonality analysis using "yhat" package but I have been getting error and I realized the rcc output is slightly different from CCA output. Can anyone help me on how to go about it please?
Hello to all.
I have a 600 surveys matrix data containing 34 response variables and 16 explaining variables. In our survey we asked respondents to give a score (from 1 to 5) to 34 species (response variables) and the 16 explaining variables are qualitative variables (gender, age ranges, job, etc). Our main goal is to see how the explaining variables influence respondents preferences for species.
I decided to apply a CCA to obtain a biplot containing the centroids of the response variables and the explaining variables. In the results I've obtained the next result:
Partitioning of scaled Chi-square:
Inertia Proportion
Total 0.10006 1.0000
Constrained 0.01200 0.1199
Unconstrained 0.08807 0.8801
As far as I know, this means that the explicative variables doesn't influence to much on the response variables.
The question is: should I keep this CCA? or should I perform an unconstrained analysis like a correspondence analysis.?
Thank you!
A common practice in community ecology studies based on multivariate techniques such as CCA, RDA, dbRDA, etc. is to try to define a parsimonious model using procedures based on p-values and R squared (e.g. forward, backward, stepwise selection).
In my experience, the parsimonious model generally "loses" most of the variable contained in the full model although retaining a similar explanatory power compared to the full model (almost the same R2). Although this seems statistically meaningful, when plotting the triplot of the full model one is able to understand much more of the ecological "story" compared with the parsimonious. For example, the gradients in the site and species are much more clear and so the relationship between species, sites and constraints.
I think this is mostly philosophy, but someone has any consideration on it?
NB: I am referring to models in which collinearity between variables is absent.
In multivariate analysis to determine the effect of environmental factors on plants, when to use RDA, and when to use CCA?
Hello!
For my thesis I have been collecting data concerning fish biomass, species richness/diversity among several marine habitats. I would like to perform a MVA to compare the species found at the 6 different marine habitats.
My plan was to perform a DCA and see whether I should continue with a PCA or a CCA based upon the rule of thumb introduced by Lepš & Šmilauer (2003) (to see whether the DCA axis is > 4 S.D. or < 3 S.D.). I suspect the outcome to be > 4 S.D. suggesting unimodal methods to be used next, in this case CCA.
I want to add the 6 different habitats as dummy variables (so K-1 is 5 categories represented by binary data). I am performing the analyses in R using the vegan package. I was wondering how to incorporate these dummy variables and in which steps of the analysis.
I now have rows of sites and columns with species counts (sites by species counts matrix). I added the 5 habitat categories as columns (so as the ones and zeros). Do I include the dummy variables for every step of the analysis (both DCA and CCA)? Does anyone have experience with this / some recommendations of papers?
Kind regards, Anne
Hello,
I'm trying to customize a CCA biplot made with the plt.var function from the CCA package. I need to reduce the size of the labels or be able to move those labels because they overlap on top of each other and nothing is seen in the graph. See below an example of a graph to modify. Is this possible? I cannot find a way to do it.
Thank you very much.
Ruth

As I am new to the ADANCO PLS software, I noticed that the ADANCO does not have CFA function but have CCA function. Are they the same thing? Can we report the CCA instead of CFA? If not, what is the alternative option if we use ADANCO?
Thank you for your input
Alex
Hello Everyone, I need to compare three methods of soil stability, i have to evaluate which could be most suitable method. Which kind of analysis model is best suited to evaluate which method was appropriate for these soils to evaluate their stability.
Being an undergraduate student, it is my intent to adopt a theoretical framework for use in my research work entitled 'Teachers' Competences as Determinants of Implementing Basic Cultural and Creative Arts (CCA) Curriculum in Primary Schools' but I'm yet to find an apt theory which can serve as the basis for the discourse of independent variable (teachers' competences) in my project topic. Meanwhile I found a revelant theory (performance theory) - though there was only a little explanation of it in the Nigerian national daily where it was cited in an opinion letter (The Nation: January 31, 2020) but it seems to be firmly grounded in performing theatre and arts which is why I am not sure whether it can be adopted or otherwise.
Kindly offer some suggestions, recommendations and/or tips with regard to my question. Thanking you in anticipation.
I study fish assemblage structures, which observed unimodal response to environmental gradient and relationships between environmental factors.
I would like to use constrained ordination methods (like RDA or CCA), which allow to use bray-curtis dissimilarity matrix.
(If I choose using RDA or CCA , I will choose CCA.)
I think CAP or db-RDA is useful for my study.
When assemblages response unimodal to environmental factors, which should I choose CAP or db-RDA?
Hello everybody, can you help me to understand the difference between correspondence analysis and canonical correspondence analysis using past application and for which type of data can i use them? Thanks in advance.
Hai friends,
I have started my research recently, working on Artifacts removal EEG signal. I have done the literature survey on PCA, ICA,CCA, EMD,EEMD. I have understood somehow. Can you please tell me how to take EEG signal as input and how to get EEG database.
What is the mechanism to achieve CCA security for cp-abe using ECC instetad of bilinear mapping? What is the mechanism to mitigate key recovery attack?
I want to correlate meteorological data and particulate matter data. Can I use both the Principal Component Analysis (PCA) and Canonical Correlation Analysis (CCA)? Or is there any preliminary test to determine which one to use? Thanks!
I have a dataset from 12 river sites which contains n/100m sq of several fish species and many environmental variables relating to habitat and water quality. I'm able to ordinate site identity with habitat variables using PCA. I'm also able to ordinate fish density with site identity using NMDS. However, I wish ordinate site, density and habitat variables on a triplot to investigate how habitat differences at each site affects the density. I've read that CCA might be the solution. However, I'm finding information on running this analysis rather impenetrable.
Can anyone advise if CCA would be the best approach, or recommend a superior approach considering my data? Secondly, if anyone has any guides to running CCA or another ordination technique in r or minitab which explains the process in simple terms, I'd be very grateful to hear from you.
Dear readers,
See image: The length of the first axis is obviously >4, suggesting I should use CCA. But it's all because of the outlier 5_2.
Is that sufficient justification to use CCA?
For some reason it feels like I should apply some bias to the data set and go for an RDA instead (just by wondering the question "what if location 5_2 (which is the second of 6 habitats in location 5) wasn't in the data set.")
What do you guys think? How should I go about this?
Thanks!

I wish to analyze the effect of tillage, nitrogen and cover crops on weed communities. The design can be described as the following:
- 4 blocks
- main plot factor: tillage (nested in blocks)
- sub plot factor: nitrogen (nested in tillage)
- sub sub plot factor: cover crops (nested in nitrogen)
Hence, in a classical univariate mixed model (lme syntax), the error structure would be defined as (1|block/tillage/nitrogen) if only one sample is present at the sub sub plot level.
Now, I wish to analyse in R the effects of tillage*nitrogen*cover crops (all simple effects, all second order interactions and the third order interaction) on weed communities through partial CCA (to filter out the block effect).
I believe the following CCA model is correct (in {vegan}):
cca2013=cca(log(cover_2013+1)~tillage*N*CC+Condition(block),data=cover_2013)
And from what I gathered on the {permute} vignette, the permutation design should be defined the following way:
h<- how(within = Within(type = "free"), plots = Plots(strata = interaction(block,tillage), type = "free"), blocks = block)
Is this correct? Am I not missing an additional level of nestedness?
Finally, the significance of each term would be tested the following way:
anova(cca2013,by="terms",permutations=h)
I would be grateful if someone could provide their expertise.
Sincerely,
Guillaume ADEUX
Number of environmental variable=5
Species abundance in each sites is used as dependent variables.
Thank you
Hello there!
Im working with a community matrix (abundance data), and i would like to check if there is a taxa indicative of different trophic state of lakes. I would to that with Indval command in R.
The problem is that my data has zeros and some taxa abundance goes up to 10000 individuals per sample.
In this scenario, would it be advisable to transform my data prior to the analisys? Should i use a Hellinger transformation?
I ask about a hellinger transformation because im thinking of doing after a CCA in this same community matrix, with some environmental data.
Any recommendation?
Thank you for your time!
I am looking for a method to assess the biomass of CCA without scraping it off the rock. Scraping CCA off the rock underwater is intense work and it often results in incomplete removal and the loss of some of the sample during the process.
Can anyone recommand an alternative?
%cover to biomass conversion tables would be an awesome way to go.
While doing pca or CCA can we keep epiphytes and lithophyte in same data sets
Hello there, i would like some advice on how to correctly perform a CCA, and if i do need to transform my data. To do so ill explain my intends abut this work and how is my data. (i'll try to be as much specific and to explain correctly in english)
Im working on a ecologic assessment using fitoplankton and environmental parameters on tropial eutrophic reservoirs. To do so i collected weekly summer samples for each site. I made a monthly mean for the biotic (density data) and abiotic parametres (Tempratura, pH, NO3, etc...). This mean, is the data that i have right now to do a CCA (60 taxons and 19 environmental variables). The taxons are in densities (Org/mL) unit, and i'm thinking abut perform a pre PCA for the abiotic parameters and biotic to exclude some data. But i'm worring about my statistical approach, if it is correctly, or if i need to do some more steps, like a data transformation in my analysis..
Dear Researchers,
I tried to plot CCA triplot using PAST v.3.2 with the same data set for a second calculation. & I experienced a difference in triplot and also in the eigen values.
In the first calculation, I got the eigen values as:
Axis Eigenvalue %
1 0.18872 75.76
2 0.060376 24.24
& in second calculation with the same data using the same software,
Axis Eigenvalue %
1 0.18202 80.37
2 0.044461 19.63
was the score!
Is it a minor/ major error? Can anybody help me to resolve this problem? & please share your experiences with PAST software, if any?
Thanks in Advance.
sincerely
Anila .P. Ajayan
I want to learn which type of li-ion cells you have choosen for automotive starter application ? Which cathode will be superior to overcome starter battery duties such as CCA, self discharge rate at elevated temperatures etc.
Best Regards.
I have site A and site B, I am getting eight Chlorophyceae species at one site and only two Chlorophyceae species at the other site. I need to do community analysis with abiotic parameters at same sites, I tried with Canonical Correspondence Analysis (CCA) but its unable to generate a plot at site B since I have only two species at this site.
I am doing CCA of taxa data with 8 explanatory variables. In the resulting triplot, those exp.var. have different lengths that represent the strength of the impact of that variable on the explained variance in the dataset. How to quantify this length/ strenght?
The DCA results are attached below.
Provide the software details?
When I get the four gradient values froma DCA,
Do I have to sum them? Or Do I have to look foor the single largest to be <4 to choose a RDA?
PRIMER is fairly costly and I can understand why many would use ordination techniques (nMDS, PCA, CCA) in R (particularly the 'vegan' package). But I was wondering if there are any differences that I ought to be concerned about (e.g. will nMDS plots from the vegan package be starkly different from the ones we get in PRIMER?)? I obviously don't have PRIMER so I can't make a comparison of results and graphs, but what makes 'vegan' in R just as good as PRIMER?
Hello,
In order to avoid re-cutting of my DNA by cas9 (after a hopefully successful knock-in), I need to change the NGG sequence in my donor plasmid. The problem is that the NGG is in the coding region of the protein and this particular codon is for proline, which means all it`s codons are essentially NGG: CCC, CCA, CCG (my PAM is in the reverse strand).
Has anyone has a creative idea of how to solve this issue? maybe change it to the amino acid most resembles Proline...?
Thanks!!
Concerns EMG artifact removal from EEG data.
Can anyone help me with the statistical analysis of my study on the diversity of algae and the effect of abiotic parameters? My data count has many zeros which I cannot use CCA or PCA. I researched online and mostly talked about using Extra Poisson Variation models which I have no idea as to how to do it. Need help desperately. This is my first time doing an ecological study for my project, am desperately in need of help.
Upon searching many literature many doubts regarding How to use CCA for downscaling of predictands.
1. How to input data into CCA?
2. How to do downscaling using CCA?
Hello!
I have attached a canonical correlation analysis (CCA) map between 10-m wind speed and rainfall over Himalayan region in this question. Please guide me, how I'll interpret this map and the time series. What is the interrelation between the three plots in the attached file?

Hi, I have a data set of around 30 sites that have braun-blanquet cover in an ordinal transformation.
I'm looking to see if species composition is affected by several variables like land management type, manure intensity, moisture level etc. and I have a few questions...
First, is a CCA graph suitable for this? Second, would it still be suitable if one of the factors was independent of the other? e.g if moisture is dependent on land management type etc. I have other analyses like ANOSIM and SIMPER for significance and similarities.
And lastly, if I were to do multiple regressions instead, would this be suitable, what's the difference really besides the fact that regressions would give us significance values? But I've already covered that with ANOSIM. I was also having trouble earlier doing regressions on braun-blanquet cover.
As we know, three algorithms (CCA system) are used in cloud detection in QA band. Is it possible to use QA band to generate cloud mask directly by setting thresholds?
Has CFMask a higher precision for cloud detection compared with CCA system, considering that CCA system is composed of three algorithms?
Should the CCA system be more precisely? This is the point where I am confused.
Details about CCA System are in Section 4.1.4.3 at http://landsat.usgs.gov/l8handbook_section4.php.
Information about CFmask at http://landsat.usgs.gov/documents/provisional_l8sr_product_guide.pdf.
Timber treated with Chromated Copper Arsenate (CCA) or Creosote is classified as hazardous waste in the UK. Has anyone conducted or know about research or analysis into whether the hazardous components degrade over time?
Hi Everyone,
I am located in Alabama and I need help with large quantity of arsenic contaminated soil for a remediation study. The higher the level of arsenic contamination the better.
i was referred to a few industries but access is a problem (it turns out no one wants to admit their soil if contaminated). I have called my regional EPA and the state’s ADEM without any luck.
If anyone has information about, or a contact at a mine, lumber treatment plant where CCA is used, or any other location with high arsenic pollution that will allow excavation of the soil for research purpose I will appreciate that a lot. Tell them I will take the bad soil off them.
Also, if you are a researcher and have access, we would like to collaborate with you on this research. You can contact me directly at oidehen1985@mytu.tuskegee.edu.
I need quite a lot for a mesocosm study.
Thank you.
I want to change CCA in ContikiMAC protocol for WSN just to handle packets at intermediate nodes. Please suggest...
There are some papers that use cca to face recognition.
I've extracted two type of features from ORL dataset, that have 400 images of 40 subjects. and, at this step by using each type of features classification accuracy is about 98%, but when i transformed feature to new space using cca, accuracy fall to just 3%.
- Where is problem?
- Are class labels not important to find directions using cca?
Thanks.
I am trying to determine how fish predator assemblage (species composition - diversity, abundance - MaxN and individual size (S,M,L) change over a distances gradient and sampling period (day, dusk, night, dawn).
My independent variables are time (fixed with four levels), tide (fixed with four levels), distance, and depth.
Would it be better to use a Permanova or a CCA?
Thank you
What is the difference between canonical correlation analysis(CCA) and multiway canonical correlation analysis(MCCA)?
After obtaining projection matrices for EEG signal using CCA, how to perform classification? (assuming there are two classes)
For Companies traded at the Stock Exchanges, Beta-Factors are available (CAPM). But most companies are not traded on the Stock Exchanges (many SMEs).
So how can the risk premium of the Equity (for the cost of capital) be calculated for an non puplic-traded company?
I and my friend conducted some research about phytoplankton abundance in some fish ponds in Yogyakarta, Indonesia. We try to use CCA using PAST version 2.17 since it can give precise visualization of how the environment controls the phytoplankton. However, this is our first time using CCA and we hope we will not mistakenly interpret this graph. Could anyone give shed some light on it?
Here attached our CCA graph
Thank you

I wanted to see the relation between species abundance and environmental parameters. I found that CCA could be a better option. But I am struggling to interpret the plot. Can any one help me in this regard?
Hello, we are working on biological traits analysis with fuzzy coding and would like to make the link with abiotic conditions.
How do you do it?
I am trying to perform a partial CCA in CANOCO 4.5. When chosing some groups of variables as variables and the rest of the environmental variables as covariables to calculate the net effect of the group, I get the error message "No explanatory variables remained" and the analysis fails. The variables in the groups could be numerical or dummy coded categorical, it happens in either case. When regrouping the respective group to another, it does increase the effect of the other group, so there should be some explanatory power! I already checked for linear combinations. All variables concerned were significant in forward selection. Does anybody have an idea what could be wrong with the data?
I haven't done habitat use studies, analyzing which local and landscape-level factors best explain bird species occurrence. for several decades, and am wondering if CCA (canonical correspondence analysis) is still considered valid (and used). Looks like most of the references are from the 1980s and 1990s, so I'd be interested to hear if some other method is used instead.