ramosvertiztraumatologiayortopediapdf33

Ramosvertiztraumatologiayortopediapdf33

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https://colab.research.google.com/drive/18TptGKZHUhUfbP-yF6KrpXC87eJCL6f0
https://colab.research.google.com/drive/15iWT2LIfyOOAZqkZrOmkAhgn99g9YK4j
https://colab.research.google.com/drive/1HiVsNxzsfKkCb9EAnvHcVmyPjYYkoEUt
https://colab.research.google.com/drive/1irBDp15zjVSHd3QovaIB_krdCCk3kJZ0
https://colab.research.google.com/drive/11khRqtpcGm3Q-v_1G0j9uatpf7gF8JwM

And from their inverse Fourier transform:

Obviously, matching the spectrograms and the inverse Fourier transform is not always easy and “perfect”, so I don’t have it and cannot give any better comparison.

A:

Looking at the spectrogram you show, if I understand correctly, the two sounds are similar, but they can be distinguished by their difference in pitch. The first sound has a ‘level’ compared to the second which is much lower. One way you can check this is to play the two audio clips and view the sound waves in the spectrum.
In the sound you show, the difference in pitch can be easily seen in the spectrum.
In the other link, there is no way to tell which audio clip was played.
The pitch in the spectrum is determined by the fundamental frequency of the signal. The louder the sound, the higher frequency it has. Once a signal has been sent to the microphone, no matter how long the original sound persisted, that part of the wave produced by the original sound will still be present. So it’s reasonable that the shorter the original sound, the lower the frequency in the spectrum.
The original sounds don’t have to be identical. The pitch difference is all that is necessary to distinguish one from the other.

Studies on the antimalarial activity and toxicity of various local anesthetic agents.
Since significant work has been done by others with regard to the mechanism of malarial antimalarial activity, and more recently on the toxicity of several local anesthetics, a study was undertaken to determine what, if any, effect these two factors have on local anesthetic activity. In preliminary studies in the rodent model, both lignocaine and prilocaine were found to be highly toxic, with LD50’s of 340 mg/kg and 34 mg/kg, respectively. In addition, lignocaine was found to have antimalarial activity, while prilocaine was found to have no antimalarial activity. On the basis of these results, other local anesthetic agents were tested. The following findings were obtained. 1) Bupivacaine and mepivacaine were found to be as toxic as prilocaine and lignocaine, respectively, and as active as prilocaine in the rodent model. 2) Dyclonine had antimalarial activity, while procaine, lidocaine, and tetracaine had no antimalarial activity. 3) Procaine
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