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MathWorks Inc piv analysis program
Transverse <t>PIV</t> frames (y–z) behind the bats flying at 6 m s−1. (a,c) Downstroke for G. soricina and L. yerbabuenae, respectively, while (b,d) the equivalent upstrokes. The symmetry line behind the bat body is indicated by the black vertical dot-dash line. The in-plane velocity vectors are shown, and the surface colour shows the stream-wise vorticity. During the downstroke, the tip-vortex is visible as the dark blue areas indicated with a grey dot in the centre, and the <t>root</t> <t>vortices</t> are the orange areas indicated with a blue dot. During the upstroke, the reversed vortex dipole is visible as the blue and red vorticity patch connected with a red bar. The vorticity colour bar ranges from −300 to 300 s−1, while vorticity below the threshold of ±60 s−1 is not shown. The reference velocity vector on the bottom left corner of (e) is equal to 10 m s−1. Panel sizes are 175 mm by 205 mm for G. soricina and 200 mm by 205 mm for L. yerbabuenae (width by height).
Piv Analysis Program, supplied by MathWorks Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/piv analysis program/product/MathWorks Inc
Average 90 stars, based on 1 article reviews
piv analysis program - by Bioz Stars, 2026-03
90/100 stars
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Image Search Results


Transverse PIV frames (y–z) behind the bats flying at 6 m s−1. (a,c) Downstroke for G. soricina and L. yerbabuenae, respectively, while (b,d) the equivalent upstrokes. The symmetry line behind the bat body is indicated by the black vertical dot-dash line. The in-plane velocity vectors are shown, and the surface colour shows the stream-wise vorticity. During the downstroke, the tip-vortex is visible as the dark blue areas indicated with a grey dot in the centre, and the root vortices are the orange areas indicated with a blue dot. During the upstroke, the reversed vortex dipole is visible as the blue and red vorticity patch connected with a red bar. The vorticity colour bar ranges from −300 to 300 s−1, while vorticity below the threshold of ±60 s−1 is not shown. The reference velocity vector on the bottom left corner of (e) is equal to 10 m s−1. Panel sizes are 175 mm by 205 mm for G. soricina and 200 mm by 205 mm for L. yerbabuenae (width by height).

Journal: Journal of the Royal Society Interface

Article Title: Comparative aerodynamic performance of flapping flight in two bat species using time-resolved wake visualization

doi: 10.1098/rsif.2011.0015

Figure Lengend Snippet: Transverse PIV frames (y–z) behind the bats flying at 6 m s−1. (a,c) Downstroke for G. soricina and L. yerbabuenae, respectively, while (b,d) the equivalent upstrokes. The symmetry line behind the bat body is indicated by the black vertical dot-dash line. The in-plane velocity vectors are shown, and the surface colour shows the stream-wise vorticity. During the downstroke, the tip-vortex is visible as the dark blue areas indicated with a grey dot in the centre, and the root vortices are the orange areas indicated with a blue dot. During the upstroke, the reversed vortex dipole is visible as the blue and red vorticity patch connected with a red bar. The vorticity colour bar ranges from −300 to 300 s−1, while vorticity below the threshold of ±60 s−1 is not shown. The reference velocity vector on the bottom left corner of (e) is equal to 10 m s−1. Panel sizes are 175 mm by 205 mm for G. soricina and 200 mm by 205 mm for L. yerbabuenae (width by height).

Article Snippet: The resulting three-component transverse PIV data ({ u, v, w } velocity matrix) are imported into a custom-made Matlab (7.7.0.471, R2008b) PIV analysis program, in which the location, vorticity and circulation of different vortices within a PIV frame can be measured.

Techniques: Plasmid Preparation