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Published: 25 July 2024

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1

Nishioka, Sotaro, Susumu Sasaki, Shunsaku Nakagawa, Mitsuharu Yashima, Hidekazu Mukuda, Mamoru Yogi, and Jun-ichi Shimoyama. "Nuclear-spin evidence of insulating and antiferromagnetic state of CuO₂ planes in superconducting Pr₂Ba₄Cu₇O_15−δ." Applied Physics Express 15, no. 2 (January 20, 2022): 023001. http://dx.doi.org/10.35848/1882-0786/ac4533.

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Abstract In contrast to the “Pr-issue” that neither PrBa2Cu3O7 (Pr123) nor PrBa2Cu4O8 (Pr124) shows superconductivity (SC), we have observed 100%-fraction of SC in an oxygen-reduced Pr2Ba4Cu7O15−δ (Pr247) which has a hybrid structure that Pr247 = Pr123 + Pr124. It is found that Cu nuclear-spin signals from the CuO2 planes observed at 300 K are completely wiped out at 2 K. Instead, the plane signals at 2 K are observed at higher frequencies. This indicates that, despite the bulk SC, the CuO2 planes in Pr247 are found to be in an insulating and antiferromagnetically ordered state.

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2

Mizokawa, T., A. Ino, T. Yoshida, A. Fujimori, C. Kim, H. Eisaki, Z. X. Shen, et al. "ARPES study of LSCO and PBCO: Electronic structure of the stripe phase and the 1/4-filled Cu-O chains." International Journal of Modern Physics B 14, no. 29n31 (December 20, 2000): 3602–9. http://dx.doi.org/10.1142/s021797920000412x.

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We have studied the electronic structure of the stripe phase in La 2-x Sr x CuO 4 (LSCO) and the Cu-O chains in PrBa 2 Cu 3 O 7 (Pr123) and PrBa 2 Cu 4 O 8 (Pr124) using angle-resolved photoemission spectroscopy (ARPES). In LSCO with x=0.12, the spectral feature near the Fermi level (EF) is almost flat from (π, 0) to (π, π/4), namely, along the stripe direction in LSCO. While the 1/4-filled chain in Pr123 has a band gap because of charge ordering, the metallic chain in Pr124 shows a dispersive feature which reaches EF at ~(π, π/4) and a flat feature near EF which is similar to that observed in the stripe phase of LSCO. Although Pr124 shows spectral-weight suppression near EF due to the instability toward charge ordering, the suppression is imperfect and Pr124 has a substantial spectral weight at EF probably due to the chain-chain coupling. This is in sharp contrast to LSCO with the perfect gap opening near (π, π/4). The difference between the stripe phase in LSCO and the coupled chains of Pr124 would be derived from the interaction between the stripe and the neighboring Cu spins which suppresses the charge ordering along the stripe.

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3

Padmanathan, S., K. Wong, J. Veerakumaran, S. Hasan, S. S, R. K. Muniandy, and V. Rai. "Abstract PR122." Anesthesia & Analgesia 123 (September 2016): 164. http://dx.doi.org/10.1213/01.ane.0000492528.64337.a2.

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4

Shosholcheva, M., N. Jankulovski, A. Kartalov, and B. Kuzmanovska. "Abstract PR127." Anesthesia & Analgesia 123 (September 2016): 168. http://dx.doi.org/10.1213/01.ane.0000492532.71961.1a.

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5

Vu, H. P., and Q. K. NGUYEN. "Abstract PR172." Anesthesia & Analgesia 123 (September 2016): 219. http://dx.doi.org/10.1213/01.ane.0000492573.46411.2d.

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6

Koyama, K., R. Nakashima, K. Magishi, T. Saito, T. Shima, and M. Hagiwara. "Superconducting behaviours in reduction-treated mixtures of fine Pr124 and Pr123 ceramics." Journal of Physics: Conference Series 320 (September 28, 2011): 012077. http://dx.doi.org/10.1088/1742-6596/320/1/012077.

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7

van Cleef, Koen W. R., Wendy M. A. Scaf, Karen Maes, Suzanne J. F. Kaptein, Erik Beuken, Patrick S. Beisser, Frank R. M. Stassen, Gert E. L. M. Grauls, Cathrien A. Bruggeman, and Cornelis Vink. "The rat cytomegalovirus homologue of parvoviral rep genes, r127, encodes a nuclear protein with single- and double-stranded DNA-binding activity that is dispensable for virus replication." Journal of General Virology 85, no. 7 (July 1, 2004): 2001–13. http://dx.doi.org/10.1099/vir.0.79864-0.

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An intriguing feature of the rat cytomegalovirus (RCMV) genome is open reading frame (ORF) r127, which shows similarity to the rep genes of parvoviruses as well as the U94 genes of human herpesvirus type 6A (HHV-6A) and 6B (HHV-6B). Counterparts of these genes have not been found in other herpesviruses. Here, it is shown that the r127 gene is transcribed during the early and late phases of virus replication in vitro as an unspliced 1·1 kb transcript containing the complete r127 ORF. Transcripts of r127 were also detected in various organs of RCMV-infected rats at 1 week post-infection (p.i.), but only in the salivary gland at 4 months p.i. Using rabbit polyclonal antibodies raised against the r127-encoded protein (pr127), pr127 was found to be expressed as early as 12 h p.i. within the nuclei of RCMV-infected cells in vitro. Expression of pr127 was also observed within the nuclei of cells in various organs of RCMV-infected rats at 3 weeks p.i. Moreover, pr127 was demonstrated to bind single- as well as double-stranded DNA. Finally, an RCMV r127 deletion mutant (RCMVΔr127) was generated, in which the r127 ORF was disrupted. This deletion mutant, however, was shown to replicate with a similar efficiency as wild-type RCMV (wt RCMV), both in vitro and in vivo. Taken together, it is concluded that the RCMV r127 gene encodes a nuclear protein with single- and double-stranded DNA-binding activity that is dispensable for virus replication, not only in vitro, but also during the acute phase of infection in vivo.

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8

Hagiwara, M., T. Shima, S. Tanaka, and K. Koyama. "Anomalous behaviors in resistivity and magnetization of reduction-treated multi phase ceramics of Pr124/Pr123 and inhomogeneous Pr247." Physica C: Superconductivity and its Applications 470 (December 2010): S65—S67. http://dx.doi.org/10.1016/j.physc.2009.11.158.

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9

Beaver, J. S., A. González, G. Godoy‐Lutz, J. C. Rosas, O. P. Hurtado‐Gonzales, M. A. Pastor‐Corrales, and T. G. Porch. "Registration of PR1572‐19 and PR1572‐26 pinto bean germplasm lines with broad resistance to rust, BGYMV, BCMV, and BCMNV." Journal of Plant Registrations 14, no. 3 (August 20, 2020): 424–30. http://dx.doi.org/10.1002/plr2.20027.

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10

Hamdi, M., S. Boughariou, N. Sfeyhi, B. Zbidi, S. Zakhama, F. Klai, and M. Boussofara. "Abstract PR102." Anesthesia & Analgesia 123 (September 2016): 142. http://dx.doi.org/10.1213/01.ane.0000492508.35835.49.

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11

Judickas, S., M. Serpytis, G. Kezyte, I. Urbanaviciute, and E. Gaizauskas. "Abstract PR107." Anesthesia & Analgesia 123 (September 2016): 147. http://dx.doi.org/10.1213/01.ane.0000492513.66329.01.

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12

Lessa, M., T. Wellman, N. De Prost, M. Tucci, T. Winkler, G. Musch, R. Baron, B. Raby, J. Hutchinson, and M. Vidal Melo. "Abstract PR112." Anesthesia & Analgesia 123 (September 2016): 152–53. http://dx.doi.org/10.1213/01.ane.0000492518.04448.67.

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13

Nobile, L., N. Goldsztejn, J. Creteur, J. L. Vincent, and F. S. Taccone. "Abstract PR117." Anesthesia & Analgesia 123 (September 2016): 159. http://dx.doi.org/10.1213/01.ane.0000492523.33843.d2.

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14

Yen Sarn, Y., M. Hasan, M. F. H. Jamaluddin, L. Pui San, A. Amir, and V. Rai. "Abstract PR120." Anesthesia & Analgesia 123 (September 2016): 162. http://dx.doi.org/10.1213/01.ane.0000492526.56714.ce.

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15

Kamarul Zaman, M., V. Rai, M. S. Hasan, and H. Abdul Majid. "Abstract PR121." Anesthesia & Analgesia 123 (September 2016): 163. http://dx.doi.org/10.1213/01.ane.0000492527.64337.46.

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16

Schlesinger, J. "Abstract PR124." Anesthesia & Analgesia 123 (September 2016): 165. http://dx.doi.org/10.1213/01.ane.0000492529.49090.5b.

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17

Karci, O., S. Serin, and H. Sungurtekin. "Abstract PR125." Anesthesia & Analgesia 123 (September 2016): 166. http://dx.doi.org/10.1213/01.ane.0000492530.87208.a8.

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18

Shehabi, Y., M. Green, N. Taylor, M. Beaudoin, P. Grant, M. Bailey, and Z. Endre. "Abstract PR126." Anesthesia & Analgesia 123 (September 2016): 167. http://dx.doi.org/10.1213/01.ane.0000492531.94831.e0.

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19

Sungurtekin, H., S. Karakuzu, and S. Serin. "Abstract PR129." Anesthesia & Analgesia 123 (September 2016): 169. http://dx.doi.org/10.1213/01.ane.0000492533.79584.ff.

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20

Tarabrin, O., S. Shcherbakov, D. Gavrychenko, G. Mazurenko, and P. Tarabrin. "Abstract PR132." Anesthesia & Analgesia 123 (September 2016): 173. http://dx.doi.org/10.1213/01.ane.0000492536.25327.42.

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21

Yu, Y., and Y. Yu. "Abstract PR137." Anesthesia & Analgesia 123 (September 2016): 179. http://dx.doi.org/10.1213/01.ane.0000492541.88993.52.

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22

Bilskiene, D., A. Vilke, V. Traskaite, D. Bieliauskaite, and A. Macas. "Abstract PR142." Anesthesia & Analgesia 123 (September 2016): 183–84. http://dx.doi.org/10.1213/01.ane.0000492545.42359.d7.

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23

Ho, K. M., and S. Honeybul. "Abstract PR147." Anesthesia & Analgesia 123 (September 2016): 191. http://dx.doi.org/10.1213/01.ane.0000492550.49983.8c.

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24

Lai, Y. M., A. Schauer, P. De Witt Hamer, and C. Boer. "Abstract PR152." Anesthesia & Analgesia 123 (September 2016): 196. http://dx.doi.org/10.1213/01.ane.0000492554.03349.d3.

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25

Luo, F. "Abstract PR157." Anesthesia & Analgesia 123 (September 2016): 202. http://dx.doi.org/10.1213/01.ane.0000492558.77799.54.

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26

Pak, M. H., Y. Ko, S. Lee, and W. Chung. "Abstract PR162." Anesthesia & Analgesia 123 (September 2016): 207–8. http://dx.doi.org/10.1213/01.ane.0000492563.08294.6f.

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27

Krasnenkova, M., and D. Sabirov. "Abstract PR167." Anesthesia & Analgesia 123 (September 2016): 214. http://dx.doi.org/10.1213/01.ane.0000492568.15917.c4.

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28

Sookplung, P., N. Saiyarin, and P. Akavipat. "Abstract PR170." Anesthesia & Analgesia 123 (September 2016): 217. http://dx.doi.org/10.1213/01.ane.0000492571.61659.53.

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29

Unic-Stojanovic, D., V. Maravic-Stojkovic, S. Babic, P. Gajin, A. Parojcic, B. Milicic, and M. Jovic. "Abstract PR171." Anesthesia & Analgesia 123 (September 2016): 218. http://dx.doi.org/10.1213/01.ane.0000492572.69282.9f.

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30

Wang, B., Y. X. Zhu, X. W. Yang, and L. Qing-quan. "Abstract PR174." Anesthesia & Analgesia 123 (September 2016): 221–22. http://dx.doi.org/10.1213/01.ane.0000492574.54035.22.

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31

Wei, Z., and X. Shiyuan. "Abstract PR175." Anesthesia & Analgesia 123 (September 2016): 223–24. http://dx.doi.org/10.1213/01.ane.0000492575.48197.81.

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32

Xiaofen, S., and L. Juan. "Abstract PR176." Anesthesia & Analgesia 123 (September 2016): 225–26. http://dx.doi.org/10.1213/01.ane.0000492576.55821.ba.

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33

Xie, Y., and Q. Guo. "Abstract PR177." Anesthesia & Analgesia 123 (September 2016): 227. http://dx.doi.org/10.1213/01.ane.0000492577.32950.e7.

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34

Yelken, B. B., and O. Takak. "Abstract PR179." Anesthesia & Analgesia 123 (September 2016): 228. http://dx.doi.org/10.1213/01.ane.0000492578.40574.1d.

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35

Aboghanima, M., A. Sabry, and M. H. Ahmad Sabry. "Abstract PR182." Anesthesia & Analgesia 123 (September 2016): 233–34. http://dx.doi.org/10.1213/01.ane.0000492581.86315.1c.

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36

Bhasin, D. "Abstract PR187." Anesthesia & Analgesia 123 (September 2016): 241. http://dx.doi.org/10.1213/01.ane.0000492586.93938.9e.

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37

Das, A. V., B. Herekar, and K. Shenoy. "Abstract PR192." Anesthesia & Analgesia 123 (September 2016): 247–48. http://dx.doi.org/10.1213/01.ane.0000492591.24434.a0.

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38

Jain, K., V. P, J. K. makkar, S. gainder, and V. S. "Abstract PR197." Anesthesia & Analgesia 123 (September 2016): 255. http://dx.doi.org/10.1213/01.ane.0000492596.06508.b2.

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39

Hassan, W. M. N. W., S. Chandran, R. H. Mohd Zaini, and M. H. Hassan. "Abstract PR173." Anesthesia & Analgesia 123 (September 2016): 220. http://dx.doi.org/10.1213/01.ane.0000496975.84851.51.

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40

Kumar, Kishor, Kumari Neelam, Gurpreet Singh, Jyotirmaya Mathan, Aashish Ranjan, Darshan Singh Brar, and Kuldeep Singh. "Production and cytological characterization of a synthetic amphiploid derived from a cross between Oryza sativa and Oryza punctata." Genome 62, no. 11 (November 2019): 705–14. http://dx.doi.org/10.1139/gen-2019-0062.

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Oryza punctata Kotschy ex Steud. (BB, 2n = 24) is a wild species of rice that has many useful agronomic traits. An interspecific hybrid (AB, 2n = 24) was produced by crossing O. punctata and Oryza sativa variety Punjab Rice 122 (PR122, AA, 2n = 24) to broaden the narrow genetic base of cultivated rice. Cytological analysis of the pollen mother cells (PMCs) of the interspecific hybrids confirmed that they have 24 chromosomes. The F1 hybrids showed the presence of 19–20 univalents and 1–3 bivalents. The interspecific hybrid was treated with colchicine to produce a synthetic amphiploid (AABB, 2n = 48). Pollen fertility of the synthetic amphiploid was found to be greater than 50% and partial seed set was observed. Chromosome numbers in the PMCs of the synthetic amphiploid were 24II, showing normal pairing. Flow cytometric analysis also confirmed doubled genomic content in the synthetic amphiploid. Leaf morphological and anatomical studies of the synthetic amphiploid showed higher chlorophyll content and enlarged bundle sheath cells as compared with both of its parents. The synthetic amphiploid was backcrossed with PR122 to develop a series of addition and substitution lines for the transfer of useful genes from O. punctata with least linkage drag.

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41

Song, G. B., J. K. Liang, F. S. Liu, L. T. Yang, J. Luo, and G. H. Rao. "Subsolidus phase relations and crystal structures in the Pr1+xBa2−xCu3O7±δ system at 950 °C." Powder Diffraction 19, no. 4 (December 2004): 320–24. http://dx.doi.org/10.1154/1.1814981.

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Pr1+xBa2−xCu3O7±δ solid solution was investigated by means of X-ray powder diffraction and Rietveld analysis. Single-phase PrBa2Cu3O7±δ (Pr123) can be synthesized under a Pr-rich condition by sintering at 950 °C in air. The solubility of Pr1+xBa2−xCu3O7±δ solid solution is 0.08≤x≤0.80. The structure of Pr1+xBa2−xCu3O7±δ is orthorhombic for 0.08≤x<0.30, and transforms into tetragonal for 0.30≤x≤0.80. To form single-phase Pr123, the Ba sites in the Pr123 structure are partially occupied by excess Pr ions, and the smallest amount of excess Pr is x=0.08. Meanwhile, all Ba ions stay in the Ba sites.

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42

Malar C, Mathu, Jennifer D. Yuzon, Subhadeep Das, Abhishek Das, Arijit Panda, Samrat Ghosh, Brett M. Tyler, Takao Kasuga, and Sucheta Tripathy. "Haplotype-Phased Genome Assembly of Virulent Phytophthora ramorum Isolate ND886 Facilitated by Long-Read Sequencing Reveals Effector Polymorphisms and Copy Number Variation." Molecular Plant-Microbe Interactions® 32, no. 8 (August 2019): 1047–60. http://dx.doi.org/10.1094/mpmi-08-18-0222-r.

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Phytophthora ramorum is a destructive pathogen that causes sudden oak death disease. The genome sequence of P. ramorum isolate Pr102 was previously produced, using Sanger reads, and contained 12 Mb of gaps. However, isolate Pr102 had shown reduced aggressiveness and genome abnormalities. In order to produce an improved genome assembly for P. ramorum, we performed long-read sequencing of highly aggressive P. ramorum isolate CDFA1418886 (abbreviated as ND886). We generated a 60.5-Mb assembly of the ND886 genome using the Pacific Biosciences (PacBio) sequencing platform. The assembly includes 302 primary contigs (60.2 Mb) and nine unplaced contigs (265 kb). Additionally, we found a ‘highly repetitive’ component from the PacBio unassembled unmapped reads containing tandem repeats that are not part of the 60.5-Mb genome. The overall repeat content in the primary assembly was much higher than the Pr102 Sanger version (48 versus 29%), indicating that the long reads have captured repetitive regions effectively. The 302 primary contigs were phased into 345 haplotype blocks and 222,892 phased variants, of which the longest phased block was 1,513,201 bp with 7,265 phased variants. The improved phased assembly facilitated identification of 21 and 25 Crinkler effectors and 393 and 394 RXLR effector genes from two haplotypes. Of these, 24 and 25 RXLR effectors were newly predicted from haplotypes A and B, respectively. In addition, seven new paralogs of effector Avh207 were found in contig 54, not reported earlier. Comparison of the ND886 assembly with Pr102 V1 assembly suggests that several repeat-rich smaller scaffolds within the Pr102 V1 assembly were possibly misassembled; these regions are fully encompassed now in ND886 contigs. Our analysis further reveals that Pr102 is a heterokaryon with multiple nuclear types in the sequences corresponding to contig 10 of ND886 assembly.

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43

Blackstead, Howard A., and John D. Dow. "Superconductivity in PrBa2Cu3O7: Implications." International Journal of Modern Physics B 12, no. 29n31 (December 20, 1998): 2901–5. http://dx.doi.org/10.1142/s0217979298001757.

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PrBa 2 Cu 3 O 7 (Pr123) is an intrinsic superconductor with T c ≈ 90 K, as predicted and as recently confirmed by several groups who have synthesized superconducting material under conditions that minimize the number of PrBa defects. Based on evidence that the defect responsible for the failure of ordinary Pr123 to superconduct is PrBa , the cuprate-plane picture of high-temperature superconductivity must be revised.

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44

Stativko, Olesia, Elina Khachaturian, Elena Tsareva, Irina Shangina, Ksenia Maystrenko, Tatiana Antonova, and Ilya Pokataev. "PR127 REAL-WORLD USE OF CDK4/6 INHIBITORS – EFFECTIVENESS AND SUBSEQUENT THERAPIES." Breast 71 (October 2023): S59. http://dx.doi.org/10.1016/s0960-9776(23)00691-4.

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45

Fu, Dan, Guangshun Zhang, Yuhui Wang, Zheng Zhang, Hengrui Hu, Shu Shen, Jun Wu, et al. "Structural basis for SARS-CoV-2 neutralizing antibodies with novel binding epitopes." PLOS Biology 19, no. 5 (May 7, 2021): e3001209. http://dx.doi.org/10.1371/journal.pbio.3001209.

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The ongoing Coronavirus Disease 2019 (COVID-19) pandemic caused by Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) threatens global public health and economy unprecedentedly, requiring accelerating development of prophylactic and therapeutic interventions. Molecular understanding of neutralizing antibodies (NAbs) would greatly help advance the development of monoclonal antibody (mAb) therapy, as well as the design of next generation recombinant vaccines. Here, we applied H2L2 transgenic mice encoding the human immunoglobulin variable regions, together with a state-of-the-art antibody discovery platform to immunize and isolate NAbs. From a large panel of isolated antibodies, 25 antibodies showed potent neutralizing activities at sub-nanomolar levels by engaging the spike receptor-binding domain (RBD). Importantly, one human NAb, termed PR1077, from the H2L2 platform and 2 humanized NAb, including PR953 and PR961, were further characterized and subjected for subsequent structural analysis. High-resolution X-ray crystallography structures unveiled novel epitopes on the receptor-binding motif (RBM) for PR1077 and PR953, which directly compete with human angiotensin-converting enzyme 2 (hACE2) for binding, and a novel non-blocking epitope on the neighboring site near RBM for PR961. Moreover, we further tested the antiviral efficiency of PR1077 in the Ad5-hACE2 transduction mouse model of COVID-19. A single injection provided potent protection against SARS-CoV-2 infection in either prophylactic or treatment groups. Taken together, these results shed light on the development of mAb-related therapeutic interventions for COVID-19.

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46

Shakerian, R., and G. M. Kode. "PR17ï¿½*ABDOMINOPLASTY AND URINARY INCONTINENCE." ANZ Journal of Surgery 79 (May 2009): A57. http://dx.doi.org/10.1111/j.1445-2197.2009.04927_17.x.

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47

NAROZHNYI, V. N., D. ECKERT, K. A. NENKOV, G. FUCHS, K. H. MÜLLER, and T. G. UVAROVA. "PrBa2Cu3O7-y: SUPERCONDUCTING OR ANOMALOUSLY MAGNETIC?" International Journal of Modern Physics B 13, no. 29n31 (December 20, 1999): 3712–14. http://dx.doi.org/10.1142/s0217979299003738.

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In PrBa 2 Cu 3 O 7-y (Pr123) single crystals grown by the flux method the kink in the magnetic susceptibility χab(T), connected with antiferromagnetic ordering of Pr, disappears after field cooling (FC) in a field H‖ab-plane whereas the kink in χc(T) remains unchanged after FC in H‖c-axis. This seems to be connected with the coupling between the Pr and Cu(2) sublattices. The Curie constant C determined from the data reported for superconducting Pr123 crystals grown by the traveling-solvent floating zone (TSFZ), method (Zou et al, Phys. Rev. Lett., 80, 1074 (1998)) is about one half of that for our flux-grown non-superconducting crystals. Thus, we propose that concentration of Pr in TSFZ crystals seems to be about one half of the nominal concentration for Pr123. Therefore, we propose that superconductivity in TSFZ samples is connected most probably with the partial substitution of Pr by nonmagnetic Ba.

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48

Tagami, Minoru, M. Nakamura, Yoshihiro Sugawara, Yuichi Ikuhara, and Yuh Shiohara. "Interface structures of heteroepitaxially grown Pr123/Y123 and Pr123/Nd123 crystals by liquid phase epitaxy." Physica C: Superconductivity 298, no. 3-4 (April 1998): 185–94. http://dx.doi.org/10.1016/s0921-4534(97)01806-6.

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49

Khosroabadi, H., M. Modarreszadeh, P. Taheri, and M. Akhavan. "Possible Superconductivity in Ba-Rich Pr123." Journal of Superconductivity 17, no. 6 (December 2004): 749–53. http://dx.doi.org/10.1007/s10948-004-0834-4.

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50

Yonas, Wondimu, Abush Tesfaye, and Sentayehu Alamere. "Evaluation of yield performance of early maturing soybean (Glycine max L. Merill) genotypes in Ethiopia by using GGE Biplot model." International Journal of Agricultural Research, Innovation and Technology 12, no. 2 (January 24, 2023): 101–10. http://dx.doi.org/10.3329/ijarit.v12i2.64094.

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Abstract:

Genotype main effect and genotype by environment interaction biplot analysis is the best fit model for which-won-where pattern analysis, genotype, and test environment evaluation. Hence, the aim of this study was to identify stable and high-yielding soybean genotypes for production in diverse environments by using the genotype main effect and genotype by environment biplot stability model. Eighteen soybean genotypes were evaluated across six environments during the 2019 cropping season by using a randomized complete block design with four replications. Among evaluated environments and genotypes, Tiro-afeta gave the highest yield (3.71 t ha -1); while Humera gave the lowest yield (1.37 t ha-1), and genotype JM-HAR/PR142-15-SB gave the highest mean grain yield of 2.9 t ha -1 across the six locations. Based on the information generated from the GGE biplot, Tiro Afeta and Areka were identified as ideal environments, whereas genotypes PR-143-(14), JM-HAR/G99-15-SD-2 and JM-HAR/PR142-15-SB were ideal genotype. The ‘which won where’ biplot of the GGE analysis revealed that the six environments grouped into three different mega-environments with different winning genotypes. Among the testing environments, Areka, Sirinka and Humera grouped into one mega environment; while Tiro afeta grouped into the second mega environment and Jimma and Hawasa were classified into the third mega environment with the winning genotypes JM-HAR/PR142-15-SB, PR-143-(14) and KS4895 for each mega environment, respectively. Based on the GGE biplot stability model used in the study, JM-HAR/G99-15-SD-2, JM-HAR/PR142-15SB, and PR-143-(14) were high yielder and stable genotypes. Hence, these genotypes were recommended for variety verification and release after additional evaluation for more seasons. Int. J. Agril. Res. Innov. Tech. 12(2): 101-110, December 2022

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