I´ve been contacted last week by a student with the same complaint....

On 10/20/06, *morphmet* <[EMAIL PROTECTED]
<mailto:[EMAIL PROTECTED]>> wrote:

    Hello, morphmet list,

    When I zoom in and out in tpsDIG, the dots shift. This defeats the
    purpose, obviously, so I'm guessing I'm either missing a function that
    the program offers, or else the idea is that one shouldn't place
    landmarks on different parts of the same image at different
    magnifications. (The specimens are helically coiled snail shells, and
    the features in the earlier whorls - though putatively homologous - are
    vastly tinier than in the later coils, so being able to zoom in at the
    top would really help.) Can someone shed some light on this?

    Thanks,
    Leah Reilly
    (CUNY EEB Ph.D. student)

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-- 
Diego Astúa de Moraes, D.Sc.
Departamento de Zoologia - CCB
Universidade Federal de Pernambuco
Av. Professor Moraes Rego, s/n.
Cidade Universitária
50670-420 Recife, PE
Fone(fax): (81) 2126-8353
email: [EMAIL PROTECTED] <mailto:[EMAIL PROTECTED]> -
[EMAIL PROTECTED] <mailto:[EMAIL PROTECTED]>

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