1,066 research outputs found

    Enneapterygius hsiojenae Shen and Wu 1994

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    247. Enneapterygius hsiojenae Shen and Wu, 1994:11, fig. 7 Holotype: NTUM 07828 (29.3), Wen–tz–ken, 21 May 1991. Paratype: NTUM 02829 (1, 25.9), same as holotype; NTUM 07826 (1, 29.5), Wen–tz–ken, 18 Jul. 1990; NTUM 07827 (1, 28.0), Ba–do–tz, 7 Mar. 1991; NTUM 07849 (1, 27.3), Ba–do–tz, 7 Mar. 1991; USNM 329660 (formly NTUM 7850, 1, 29.5), Ba–do–tz, 7 Mar. 1991. Remark. This species was synonymized with Enneapterygius vexillarius Fowler by Fricke (1997). Chiang and Chen (2008) resurrected it as a valid species.Published as part of Ho, Hsuan-Ching & Shao, Kwang-Tsao, 2011, 2957, pp. 1-74 in Zootaxa 2957 on page 5

    Enneapterygius erythrosoma Shen and Wu 1994

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    245. Enneapterygius erythrosoma Shen and Wu, 1994:7, fig. 5 Holotype: NTUM 07815 (27.2), Wen–tz–keng, 21 Mar. 1991. Paratype: NTUM 07816 (1, 26.0), NTUM 07852 (1, 25.1), USNM 329658 (formly NTUM 7853, 1, 25.0), all collected with holotype; NTUM 07854 (1, 24.4), Liu–chiu, 8 Nov. 1990. Remark. Originally described with the authorship as Shen and Wu. This species was synonymized with Enneapterygius rubicauda Shen and Wu by Fricke (1997). However, Chiang and Chen (2008) resurrected it as a valid species.Published as part of Ho, Hsuan-Ching & Shao, Kwang-Tsao, 2011, 2957, pp. 1-74 in Zootaxa 2957 on page 5

    Enneapterygius leucopunctatus Shen and Wu 1994

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    248. Enneapterygius leucopunctatus Shen and Wu, 1994:12, fig. 8 Holotype: NTUM 07823 (32.3), Wen–tz–keng, 21 mar. 1991. Paratype: NTUM 7851 (1, 29.0), same as holotype; NTUM 07852 (1, 32.3), same as holotype. Remark. This species was synonymized with Enneapterygius vexillarius by Fricke (1997). However, Chiang and Chen (2008) resurrected it as a valid species.Published as part of Ho, Hsuan-Ching & Shao, Kwang-Tsao, 2011, 2957, pp. 1-74 in Zootaxa 2957 on page 5

    PIF4 regulates Al-induced local auxin signaling in root-apex TZ.

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    (A) Five-day old DR5rev:GFP and DR5rev:GFP/pif4-101 transgenes were exposed or not (control) to 25 μM AlCl3 for 2hours. Cell boundaries appear red following propidium iodide staining. The root-apex TZ is marked by white arrowheads. Scale bar: 100μm. (B) Quantification of the Al-induced fluorescence intensity in the root-apex TZ of DR5rev:GFP and DR5rev:GFP/pif4-101 seedlings. The detected fluorescence region in TZ is marked by yellow rectangles. Cell boundaries appear red following propidium iodide staining. The TZ is marked by white arrowheads. Error bars indicate mean ±SD (n≥25). Statistical difference from detected fluorescence is indicated by asterisks (Fisher’s exact test, **P < 0.01).</p

    YUCs regulate Al induced local auxin response in root TZ.

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    (A) Five-day old DR5rev:GFP, DR5rev:GFP/yuc9, DR5rev:GFP/yuc8 yuc9 and DR5rev:GFP/yucQ seedlings were exposed or not (control) to 25 μM AlCl3 for two hours. Four-day old transgenic DR5rev:GFP seedlings were pre-treated with 10 μM yucasin for 1 day, then were co-treated with 25 μM AlCl3 for two hours or not (control). The upper row shows expression of DR5rev:GFP, DR5rev:GFP/yuc9, DR5rev:GFP/yuc8 yuc9 and DR5rev:GFP/yucQ controls while the lower row shows the expression of these transgenic seedlings exposed to 25 μM AlCl3. Cell boundaries appear red following propidium iodide staining. The root-apex TZ is marked by white arrowheads. Scale bar: 100 μm. (B) Quantification of the Al-induced fluorescence intensity in the TZ of DR5rev:GFP, DR5rev:GFP/yuc9, DR5rev:GFP/yuc8 yuc9, DR5rev:GFP/yucQ and 10 μM yucasin pre-treated DR5rev:GFP seedlings (around 30 seedlings were measured in each material). The detected fluorescence region in TZ is marked by yellow rectangles. Cell boundaries appear red following propidium iodide staining. The TZ is marked by white arrowheads. Statistical difference from detected fluorescence is indicated by asterisks (Fisher’s exact test, ***P < 0.001).</p
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