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) -- Replies will be sent to the list. For more information visit http://www.morphometrics.org
