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Optimisation of pom.xml

After searching the site I have finally managed to make a pom.xml file for my GWT application that bundles all my JAR files into 1 war file.
It works fine, but it takes about two minutes to compile. It is a 500k line file. I have been looking in to techniques to see if this might be optimised. The only thing I have yet managed to do is:
– remove the Compile Dependencies from the pom.xml.
– Make sure that all the JAR files are on the default classpath.
– change the “Default goal” to “package”.

Is there anything else that I should be doing?
Also, how can I run a static analysis on the pom.xml file? Something like: Maven Analyser Plugin would be perfect (I just want to be sure I haven’t made any serious errors).

A:

You can use the checkstyle plugin for that, it supports many different options for use with javac, including separate configuration for each package to be checked. The mentioned example below checks the default package, the package you have specified in maven-compiler-plugin, and each class that resides in the default package in one go.

${basedir}

**/*.java

${project.build.directory}/classes

Last year, I wrote about the recent (and

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https://colab.research.google.com/drive/1J2oFSCK3NvHPKA_9nCD9KaiGbV61ueEn

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Muscarinic cholinoceptive nerve fibers have been found in smooth muscle of the fundus and antrum of human stomach. These fibers constituted 17% of the total number of gastric cholinergic fibers. Nicotine acetylcholine (ACh) induced a biphasic contraction of isolated canine gastric muscle in a dose-dependent manner. The maximal response was observed at a nicotine dose of 1 microM. The cholinergic contractions were reduced by atropine, hexamethonium, phentolamine, tetrodotoxin, indomethacin, and NG-monomethyl-L-arginine. The pD2 values were 6.3 and 5.6 for ACh and phenylephrine, respectively. The contractile responses to carbachol and oxotremorine were also inhibited by NG-monomethyl-L-arginine. Maximal ACh contractions were induced at low concentrations of agonists and were rapidly desensitized by prolonged exposure to agonists. ACh stimulation gave rise to release of 3H-acetylcholine (ACh), 45Ca from prelabelled smooth muscle. The release of 3H-ACh was not influenced by pretreatment with atropine. The release of 45Ca was inhibited by tetrodotoxin and by the specific calcium antagonist, verapamil, but was not affected by atropine.// ***************************************************************************
// *
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