Find research datasets worth reusing

FIGURE 29 in Notes on Neoperla sinensis Chu, 1928 and Neoperla anjiensis Yang & Yang, 1998 with descriptions of new species of Neoperla from China (Plecoptera: Perlidae)

FIGURE 29. Neoperla anjiensis Yang & Yang, 1998, aedeagus. A–B lateral; C ventral; D dorsal.

FIGURE 11 in Notes on Neoperla sinensis Chu, 1928 and Neoperla anjiensis Yang & Yang, 1998 with descriptions of new species of Neoperla from China (Plecoptera: Perlidae)

FIGURE 11. Neoperla huangshana sp. nov., male terminalia. A dorsal; B ventral; C lateral.

FIGURE 23 in Notes on Neoperla sinensis Chu, 1928 and Neoperla anjiensis Yang & Yang, 1998 with descriptions of new species of Neoperla from China (Plecoptera: Perlidae)

FIGURE 23. Neoperla pangi sp. nov., male terminalia. A the procces on terga 7–8; B left tergum 10.

FIGURE 22 in Notes on Neoperla sinensis Chu, 1928 and Neoperla anjiensis Yang & Yang, 1998 with descriptions of new species of Neoperla from China (Plecoptera: Perlidae)

FIGURE 22. Neoperla pangi sp. nov., male terminalia. A dorsal; B lateral.

FIGURE 17 in Notes on Neoperla sinensis Chu, 1928 and Neoperla anjiensis Yang & Yang, 1998 with descriptions of new species of Neoperla from China (Plecoptera: Perlidae)

FIGURE 17. Neoperla huangshana sp. nov., egg. A lateral view; B caudal view.

FIGURE 19 in Notes on Neoperla sinensis Chu, 1928 and Neoperla anjiensis Yang & Yang, 1998 with descriptions of new species of Neoperla from China (Plecoptera: Perlidae)

FIGURE 19. Neoperla huangshana sp. nov., mouthparts of nymph (right mandible and lacinia).

opencc-zeroMay 2022View details →

Supplementary material 1 from: Homberger L, Xu J, Brandis D, Chan T-Y, Keirsebelik H, Normant-Saremba M, Schoelynck J, Chu KH, Ewers-Saucedo C (2022) Genetic and morphological evidence indicates the persistence of Japanese mitten crab mitochondrial DNA in Europe for over 20 years and its introgression into Chinese mitten crabs. NeoBiota 73: 137-152. https://doi.org/10.3897/neobiota.73.72566

Table S1. Master spreadsheet with morphological and genetic information for each specimen

N2YCH CHU 7.850 MHz from April 8, 2024 Solar Eclipse

Radio: Elecraft KX2 GPS-disciplined: No AGC: On Antenna: I used a Chelegance MC-750 in a vertical configuration Lat/lon: <table> <tbody> <tr> <td>44.24017632</td> <td>-73.29627406</td> </tr> </tbody> </table> QRM: I transmitted from another vertical on 20m FT8 nearby. I hope it did not affect the reception on 40meters Notes: Sorry I didn't know to turn off the AGC...I could have but checking the radio it was on and in the fast mode. I did a POTA activation and was running FT8 on 20 meters nearby but I hope it was far enough away from 40 meters to not have an effect. If you see de-sensing every 15 seconds, that would be me. Doing this at a state park in Vermont, I ended up needing to explain what I was doing about 100 times...people certainly were accepting of the fact and even wowed when I explained I was participating in a propagation study of radio waves during the eclipse. I even had people help me carry my bags in and out of the park...thanks for letting me participate. I hope my data helps the cause.

opencc-by-4.0Jun 2024View details →

KE8UZF CHU 7.850 MHz from April 8, 2024 Solar Eclipse

Radio: Hermes14 (Apache Labs) GPS-disciplined: Yes AGC: Off Antenna: SWL Antenna 13.8 m long 6 m high, axis approx n-s with active antenna tuner ~10dB Lat/Lon: <table> <tbody> <tr> <td>43.0053</td> <td>-83.7066</td> </tr> </tbody> </table> Notes: 04/12 UTC1500 FMT had lost its 1000Hz setting, and was reset to 1000Hz upload difficulty, apparently fixed here by relaxing Netgear router settings

VA3ROM CHU 3.330 MHz from April 8, 2024 Solar Eclipse

Note: VA3ROM collected data on multiple frequencies. Radio: RX-888 MKII SDR (modified for GPSDO) GPS-disciplined: Yes AGC: Off Antenna: Ground-mounted self-resonant 40m dipole with radials (works well down to 630m) Lat/lon:  <table> <tbody> <tr> <td>48.453</td> <td>-89.20946</td> </tr> </tbody> </table>

W3OA CHU 3.330 MHz from April 8, 2024 Solar Eclipse

Note: W3OA recorded on multiple frequencies. WE2S also contributed to this data collection.  Radio: Yaesu FTDX5000 GPS-disciplined: No AGC: On Antenna: Dipole, N-S Lat/lon: <table> <tbody> <tr> <td>35.57851</td> <td>-80.9475</td> </tr> </tbody> </table>

W7GLF CHU 3.330 MHz from April 8, 2024 Solar Eclipse

Radio: Yaesu FT-817 GPS-disciplined: Yes AGC: Off Antenna: Dipole North-South Lat/lon: <table> <tbody> <tr> <td>47.711098</td> <td>-122.224053</td> </tr> </tbody> </table> Notes: Fun project

opencc-by-4.0Aug 2018View details →

Figure 2 from: Dong Z, Shi C, Chu G, Dong Y, Chen G, Liu D (2018) Morphological changes of gonad and gene expression patterns during desexualization in Dugesia japonica (Platyhelminthes: Dugesiidae). Zoologia 35: 1-7. https://doi.org/10.3897/zoologia.35.e21933

Figure 2 Sagittal section of testis during starvation. The blue lines indicate the innermost region and the yellow lines indicate that the border between the testis region and the surrounding tissue. d: days after starvation, sg: spermatogonium, sc: spermatocyte, st: spermatid, sp: spermatozoa. Scale bar: 100 μm.

opencc-by-4.0Aug 2018View details →

Figure 1 from: Dong Z, Shi C, Chu G, Dong Y, Chen G, Liu D (2018) Morphological changes of gonad and gene expression patterns during desexualization in Dugesia japonica (Platyhelminthes: Dugesiidae). Zoologia 35: 1-7. https://doi.org/10.3897/zoologia.35.e21933

Figure 1 Histological changes of the ovary during starvation. The ovary of on the day 25th is sagittal section and the others are horizontal section. The yellow lines indicate the innermost region and the oogoniums marked by black arrows, d: days after starvation, og: oogonium, oc: oocyte. Scale bar: 200 μm.

opencc-by-4.0Aug 2018View details →

Figures 3-6 from: Dong Z, Shi C, Chu G, Dong Y, Chen G, Liu D (2018) Morphological changes of gonad and gene expression patterns during desexualization in Dugesia japonica (Platyhelminthes: Dugesiidae). Zoologia 35: 1-7. https://doi.org/10.3897/zoologia.35.e21933

Figures 3-6 The time-course expressions of four genes during starvation by real-time PCR: (3) Djprps; (4) DjvlgA; (5) DjvlgB; (6) Djnos. The expression levels on the day 6th after the last feeding were used as the control, β-actin was used as inter-control. d: days after starvation. Vertical bars represented the mean ± SD (N = 3). Asterisks indicate statistical differences (*p < 0.05, **p < 0.01).

Figure 8 from: Dai D-Q, Wijayawardene NN, Tang L-Z, Liu C, Han L-H, Chu H-L, Wang H-B, Liao C-F, Yang E-F, Xu R-F, Li Y-M, Hyde KD, Bhat DJ, Cannon PF (2019) Rubroshiraia gen. nov., a second hypocrellin-producing genus in Shiraiaceae (Pleosporales). MycoKeys 58: 1-26. https://doi.org/10.3897/mycokeys.58.36723

Figure 8 Hypocrella bambusae (K(M)52469, isotype, images are accredited to the Royal Botanic Gardens, Kew) A, C fruiting bodies on inflorescence of bamboo B vertical section of stromata showing the perithecia locating D herbarium envelope E filiform ascospores F asci with caps (Staining by cotton blue). Scale bars: 5 mm (A), 200 μm (B), 2 mm (C), 20 μm (E, F).

Figure 7 from: Dai D-Q, Wijayawardene NN, Tang L-Z, Liu C, Han L-H, Chu H-L, Wang H-B, Liao C-F, Yang E-F, Xu R-F, Li Y-M, Hyde KD, Bhat DJ, Cannon PF (2019) Rubroshiraia gen. nov., a second hypocrellin-producing genus in Shiraiaceae (Pleosporales). MycoKeys 58: 1-26. https://doi.org/10.3897/mycokeys.58.36723

Figure 7 Rubroshiraia bambusae (HKAS102255, holotype) A fruiting bodies B, C surface of ascostromata showing the openings of ostiole D vertical section of ascostromata E, F vertical section of locule G peridium of locule H asci and pseudoparaphyses I asci and asci ocular chamber J ascospores K, L immature asci. Scale bars: 1 cm (A), 25 mm (B), 2 mm (C, D), 500 μm (E, F), 200 μm (G), 50 μm (H–L).

Figure 5 from: Dai D-Q, Wijayawardene NN, Tang L-Z, Liu C, Han L-H, Chu H-L, Wang H-B, Liao C-F, Yang E-F, Xu R-F, Li Y-M, Hyde KD, Bhat DJ, Cannon PF (2019) Rubroshiraia gen. nov., a second hypocrellin-producing genus in Shiraiaceae (Pleosporales). MycoKeys 58: 1-26. https://doi.org/10.3897/mycokeys.58.36723

Figure 5 The UV spectrum of the standards and of hypocrellin A and B from the samples (Shiraia bambusicolaHKAS 102253 and Rubroshiraia bambusaeHKAS 102255) were recorded in alcohol at room temperature. HA: hypocrellin A, HB: hypocrellin B.

Figure 6 from: Dai D-Q, Wijayawardene NN, Tang L-Z, Liu C, Han L-H, Chu H-L, Wang H-B, Liao C-F, Yang E-F, Xu R-F, Li Y-M, Hyde KD, Bhat DJ, Cannon PF (2019) Rubroshiraia gen. nov., a second hypocrellin-producing genus in Shiraiaceae (Pleosporales). MycoKeys 58: 1-26. https://doi.org/10.3897/mycokeys.58.36723

Figure 6 Shiraia bambusicolaA–J sexual morph A fruiting bodies (HKAS102253, HKAS102254, HKAS102257, HKAS102261, HKAS102262) B–J photographs from material HKAS102253 B Surface of ascostromata showing the dark openings of ostiole C vertical section of ascostromata D vertical section of locule E pseudoparaphyses F, G asci (G Showing the fissitunicate asci) H–J ascospores K–M asexual morph K vertical section of asexual locules L–M conidia. Scale bars: 2 cm (A), 5 mm (B), 1 mm (C), 100 μm (D, K), 50 μm (F, G), 20 μm (H–J, L, M).

Figure 4 from: Dai D-Q, Wijayawardene NN, Tang L-Z, Liu C, Han L-H, Chu H-L, Wang H-B, Liao C-F, Yang E-F, Xu R-F, Li Y-M, Hyde KD, Bhat DJ, Cannon PF (2019) Rubroshiraia gen. nov., a second hypocrellin-producing genus in Shiraiaceae (Pleosporales). MycoKeys 58: 1-26. https://doi.org/10.3897/mycokeys.58.36723

Figure 4 Hypocrellin A and hypocrellin B HPLC-UV profiles (265 nm) of standards and stromatal HPLC-UV profiles (265 nm) of specimens of Shiraia bambusicola (HKAS 102253) (II) and Rubroshiraia bambusae (HKAS 102255) (III) and DAD spectra of major metabolites.