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...1, split = c(1,1,2,2), more = TRUE) plot(hco32, split = c(1,1,2,2), more = TRUE) plot(hco33, split = c(1,2,2,2), more = TRUE) plot(hco34, split = c(2,2,2,2), more = FALSE) dev.off() If the error is not apparent to you, please suggest what I could try to isolate the cause. Rich -- Richard B. Shepard, Ph.D. | Integrity - Credibility - Innovation Applied Ecosystem Services, Inc. | Helping Ensure Our Clients' Futures <http://www.appl-ecosys.com> Voice: 503-667-4517 Fax: 503-667-8863

...s) end end undefined method `stringify_keys!'' for "33":String Parameters: {"commit"=>"Edit", "product"=>{"image_url"=>"shep.jpg", "price"=>"400.00", "title"=>"German Shepard Lab Mix #2b", "category_ids"=>["6"], "picture_attributes"=>{"33"=>{"title"=>"asdf2"}, "24"=>{"title"=>"asdf"}, "27"=>{"title"=>"asdf"}, "30"...

I read in ?na.omit that it returns the object with incomplete cases removed. I interpret this to mean that any zoo object row where any column shows 'NA' will be removed from the data set. That's not what I need, since the 'NA' represents information in my context. However, what I would like to do is eliminate the rows where every column is 'NA'. When I aggregate

With multiple panels in a lattice trellis plot the sequence is, for example, 1, 10, 11, 12, 2, 3, 4. I want the sequence to be 1, 2, 3, 4, 10, 11, 12. Reading ?strip.default and the appropriate section in the Lattice book I'm not seeing how to specify the 'human' numeric order rather than the computer numeric order. A pointer will be appreciated. TIA, Rich

Before re-inventing the wheel I would like to ask: does anyone know about an optimizer in R which can reliably identify which value of X (Xopt) leads to Y (Yopt) closest to Ytarget in Y <- MonotoneStepFun(X) optionally with the restriction that Yopt <= Ytarget (at least if any Y <= Ytarget, otherwise any Yopt > Ytarget would be the preferred answer) If none is known, I will write

Yesterday I changed the headers for a couple of columns in data text files and removed hyphens from within character strings, too. When I tried to re-read these data sources using read.table() I encountered an issue I've not before seen. Both files were read almost instantly until yesterday's wording changes. Now both files seem to cause R to hang. Rather than having the prompt

I have installed Suse on an IBM as400 (powerpcc). This is SuSe 8.0 gcc 3.2 and with both samba 3.0.0 and 3.0.1pre3 I get this error message on the compile. (configure runs fine. make Using FLAGS = -g -O2 -I./popt -Iinclude -I/home/rshepard/samba-3.0.0/source/include -I/home/rshepard/samba-3.0.0/source/ubiqx -I/home/rshepard/samba-3.0.0/source/smbwrapper -I. -D_LARGEFILE64_SOURCE -D_FILE_OFFSET_BITS=64 -D_GNU_SOURCE -I/home/rshepard/samba-3.0.0/source LIBS = -lcrypt -lattr -lresolv -lnsl -ldl LDSHFLAGS = -shared LDFLAGS = Ge...

I have a reshaped data frame with value column headings concatenated from two column headings in the melted data frame. I want to change all 56 headings in a single command, but 'names' allows me to change only one at a time. In Hadley's 2007 article on reshape in the Journal of Statistical Software he mentions a 'rename' function, but I cannot find that. Is there a way to

The bio.infer package contains a data frame /usr/lib/R/library/bio.infer/data/itis.ttable.rda that needs to be modified. After loading the bio.infer package and attaching the data frame with the data() function, I wrote the data frame to a text file. After adding another row to the data frame I applied read.table() to create a data frame, but it's in my pwd, not the R library data

I have a data frame called chemdata with this structure: > str(chemdata) 'data.frame': 14886 obs. of 4 variables: $ site : Factor w/ 148 levels "BC-0.5","BC-1",..: 104 145 126 115 114 128 124 2 3 3 ... $ sampdate: Date, format: "1996-12-27" "1996-08-22" ... $ param : Factor w/ 8 levels "As","Ca","Cl",..:

I have a data frame with 1 factor, one date, and 37 numeric values: str(waterchem) 'data.frame': 3525 obs. of 39 variables: site : Factor w/ 64 levels "D-1","D-2","D-3",..: 1 1 1 1 1 ... $ sampdate : Date, format: "2007-12-12" "2008-03-15" ... $ CO3 : num 1 1 6.7 1 1 1 1 1 1 1 ... $ HCO3 : num 231 228 118 246

I need to understand how and why dcast() adds NAs to a data frame that contained no missing values. The database table of chemical concentrations has all missing values removed because they cannot contribute to data analyses. The structure of the R data frame of these data have no NA values, and neither does the data frame resulting from applying the reshape2 melt() function to it. However,

I would appreciate pointers on what I should read to understand this output: summary(lm(TDS ~ Cond + Ca + Cl + Mg + Na + SO4)) Call: lm(formula = TDS ~ Cond + Ca + Cl + Mg + Na + SO4) Residuals: ALL 1 residuals are 0: no residual degrees of freedom! Coefficients: (6 not defined because of singularities) Estimate Std. Error t value Pr(>|t|) (Intercept) 125 NA

On Samba-digest, Richard M. Shepard wrote > Message: 1 > Date: Sat, 12 Oct 2002 11:14:42 -0600 (MDT) > From: Robert M Shepard <bob@rmshep.mt.net> > To: samba@lists.samba.org > Subject: [Samba] rpcclient error > > > I am setting up a linux box (redhat 7.3) to server as a printer server on > a windo...

Hello, I am using t-test to check if the difference between two poulations is significant. I have a large N=20,000, 10,000 in each population. I compare a few different poulations with eachother and though I get different t-scores, I get the same p-value of 10^-16 which seems like the limit for this function. Is this true and is so, is there a workarounf to get a more sensitive/accurate p-value?

If there's a separate ESS user mail list, please point me to it. I'm using emacs with ESS and want to enter multiline commands for plots. Examples in my reference books show each line terminating with a comma so labels and other attributes can be specified for the plot before it is submitted for rendering. When I try to do this, however, I get an error: > boxplot(chemdata$quant ~

...a-2.04b was installed from the rpm. I'm using Carter and Sharpe's "Teach Yourself Samba in 24 Hours" as my guide. On page 59, they suggest testing the installation to see if the shares defined in /etc/smb.conf are correct. Here is what I run and the results returned: [root@salmo rshepard]# /usr/bin/smbclient -L salmo -N Added interface ip=192.168.55.1 bcast=192.168.55.255 nmask=255.255.255.0 session setup failed: ERRSRV - ERRbadpw (Bad password - name/password pair in a Tree Connect or Session Setup are invalid.) The win98 virtual machine is not running; makes no difference if i...

...e sort of bitkeeper to anoncvs gateway be set up so that I could check out the most recent version without having to install bitkeeper?) (I''m newly subscribed to this list. If this has already been dealt with, then I failed to figure out what message to read in the archives.) -Tim Shepard shep@alum.mit.edu _______________________________________________ LARTC mailing list / LARTC@mailman.ds9a.nl http://mailman.ds9a.nl/mailman/listinfo/lartc HOWTO: http://lartc.org/

On Mon, 22 Jan 2024, Rich Shepard wrote: > As an aquatic ecologist I see regulators apply the geometric mean to > geochemical concentrations rather than using the arithmetic mean. I want to > know whether the geometric mean of a set of chemical concentrations (e.g., > in mg/L) is an appropriate representation of the ex...

A data frame has one factor, one date, and one numeric column. When I plot these using the default pch of the open circle (first attachment), xyplot(TDS ~ sampdate | she.s, data = sheep.cast, main = 'TDS in Sheep Creek', ylab = 'Concentration (mg/L)', xlab = 'Time') I see the higher concentration points toward the right on several panels. But, when I change to using a