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. 2013 Apr 8;110(20):8224–8229. doi: 10.1073/pnas.1220285110

Fig. 1.

Fig. 1.

MIP triggers larval settlement behavior in Platynereis. (A) Angular histograms of the displacement vectors of swimming tracks for larvae treated with DMSO (control) and larvae treated with the indicated peptide [n > 100 larvae (55–60 hpf) each]. (B) Percentage of time in which cilia are closed in DMSO-treated larvae (control) vs. larvae exposed to MIP7 [n > 10 larvae (48–50 hpf) each]. (C) Percentage of 1-, 2-, 5-, and 6-dpf larvae that showed sustained substrate contact after 2 min exposure to DMSO (control), 20 μM MIP7 (for 1 dpf and 2 dpf), or 50 μM MIP7 (for 5 dpf and 6 dpf; n = 4 repetitions with >30 larvae). (D) Percentage of larvae that showed sustained substrate contact after 90 min exposure to DMSO (control), AKYFLamide (FLa), and MIP7 [n = 10 repetitions with >30 larvae (50 hpf) each]. In A, the P values of an χ2 test comparing the number of upward and downward swimming larvae are indicated as *P < 0.05 and ***P < 0.001. Data in BD are shown as mean ± SEM. P values of an unpaired t test are indicated as *P < 0.05, **P < 0.01, and ***P < 0.001, with “ns” indicating P > 0.05.