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Table A.1
Investigated β Pictoris members and member candidates.
| Simbad | α | δ | d | Reference for | Memb. |
| name | (J2000) | (J2000) | [pc] | distance | flag |
|
|
|||||
| HD 203 | 00:06:50.08 | –23:06:27.2 | 39.39 ± 0.59 | van Leeuwen (2007) | 1 |
| RBS 38 | 00:17:23.54 | –66:45:12.5 | 39.0 ± 2.6 | Riedel et al. (2014) | 2 |
| RX J0019.7+1951 | 00:19:43.04 | +19:51:11.7 | 59.4 ± 7.9 | Schlieder et al. (2012a) | 2 |
| FK Psc | 00:23:34.68 | +20:14:28.3 | 53 ± 4 | Malo et al. (2014b) | 2 |
| 1RXS J002700.0+663025 | 00:27:02.83 | +66:30:39.0 | 56.9 ± 8.3 | Schlieder et al. (2012a) | 3 |
| GJ 2006 A | 00:27:50.23 | –32:33:06.4 | 33.2 ± 2.8 | Riedel et al. (2014) | 1 |
| GJ 2006 B | 00:27:50.35 | –32:33:23.9 | 31.5 ± 2.4 | Riedel et al. (2014) | 1 |
| LP 525–39 AB | 00:32:34.81 | +07:29:27.1 | 41.1 ± 4.4 | Schlieder et al. (2012b) | 2 |
| EROS–MP J0032–4405 | 00:32:55.84 | –44:05:05.8 | 26.1 ± 2.0 | Gagné et al. (2014) | 2 |
| 2MASS J00464841+0715177 | 00:46:48.41 | +07:15:17.7 | 33.8  |
Gagné et al. (2015) | 2 |
| TYC 2288–758–1 | 00:48:28.65 | +36:32:34.5 | 61.4 ± 8.4 | Schlieder et al. (2012a) | 2 |
| RX J0102.8+1857 | 01:02:50.99 | +18:56:54.2 | 40.9 ± 4.4 | Schlieder et al. (2012a) | 2 |
| TYC 5853–1318–1 AB | 01:07:11.93 | –19:35:36.2 | 54 | McCarthy & White (2012) | 2 |
| LP 467–16 AB | 01:11:25.42 | +15:26:21.5 | 21.8 ± 0.8 | Riedel et al. (2014) | 1 |
| 2E 327 AB | 01:13:28.17 | –38:21:02.5 | 29 ± 2 | Malo et al. (2014a) | 2 |
| 2MASS J01294256–0823580 | 01:29:42.56 | –08:23:58.0 | 32.5 ± 3.2 | Gagné et al. (2015) | 2 |
| 1RXS J013514.2-071254 | 01:35:13.93 | –07:12:51.8 | 37.9 ± 2.4 | Shkolnik et al. (2012) | 2 |
| LP 648–20 (EX Cet B) | 01:36:55.17 | –06:47:37.9 | 24.0 ± 0.4 | Malo et al. (2014b) | 3 |
| BD+17 232AB | 01:37:39.39 | +18:35:32.7 | 52.6 | McCarthy & White (2012) | 3 |
| 1RXS J015255.9–632939 | 01:52:55.34 | –63:29:30.1 | 23.7 ± 2.4 | Gagné et al. (2014) | 2 |
| RBS 253 AB | 01:53:50.77 | –14:59:50.3 | 28 ± 2 | Malo et al. (2014a) | 2 |
| [SLS2012] PYC J02017+0117N | 02:01:46.77 | +01:17:16.2 | 63.7 ± 9.0 | Schlieder et al. (2012a) | 2 |
| [SLS2012] PYC J02017+0117S | 02:01:46.93 | +01:17:06.0 | 63.7 ± 9.0 | Schlieder et al. (2012a) | 2 |
| HD 14082 B | 02:17:24.73 | +28:44:30.5 | 27.34 ± 4.26 | van Leeuwen (2007) | 1 |
| HD 14082 A | 02:17:25.27 | +28:44:42.3 | 34.52 ± 3.43 | van Leeuwen (2007) | 1 |
| RX J0217.9+1225 | 02:17:56.01 | +12:25:26.6 | 67.9 ± 6.1 | Binks & Jeffries (2013) | 2 |
| [SLS2012] PYC J02226+3055 | 02:22:40.83 | +30:55:16.0 | 46.8 ± 5.1 | Schlieder et al. (2012a) | 2 |
| LP 353–51 | 02:23:26.63 | +22:44:06.9 | 28.7 ± 2.3 | van Leeuwen (2007) | 1 |
| HD 15115 | 02:26:16.25 | +06:17:33.1 | 45.23 ± 1.31 | van Leeuwen (2007) | 1 |
| AG Tri B | 02:27:28.05 | +30:58:40.5 | 39.95 ± 3.59 | van Leeuwen (2007) | 1 |
| AG Tri A | 02:27:29.25 | +30:58:24.7 | 39.95 ± 3.59 | van Leeuwen (2007) | 1 |
| CD–44 753 Aa,Ab | 02:30:32.41 | –43:42:23.3 | 35.7 | McCarthy & White (2012) | 3 |
| EXO 0235.2–5216 | 02:36:51.71 | –52:03:03.7 | 28.7 | Elliott et al. (2014) | 3 |
| BD+05 378 AB | 02:41:25.89 | +05:59:18.2 | 42.03 ± 2.65 | van Leeuwen (2007) | 1 |
| TVLM 831–154910 | 02:50:11.67 | –01:51:29.5 | 33.1 ± 4.9 | Gagné et al. (2015) | 2 |
| DENIS J025344.4–795913 | 02:53:44.49 | –79:59:13.3 | 28.9 |
Gagné et al. (2015) | 2 |
| TYC 1231–151–1 | 03:10:32.74 | +21:31:44.3 | 63.6 ± 8.7 | Schlieder et al. (2012a) | 2 |
| 1RXS J031052.7+183855 | 03:10:53.57 | +18:38:38.5 | 67.5 ± 9.9 | Schlieder et al. (2012a) | 2 |
| RX J0332.6+2843 ABC | 03:32:35.79 | +28:43:55.5 | 55 ± 4 | Malo et al. (2014b) | 2 |
| 2MASS J03350208+2342356 | 03:35:02.09 | +23:42:35.6 | 42.4 ± 2.3 | Shkolnik et al. (2012) | 1 |
| 1RXS J033936.7+453126 | 03:39:37.01 | +45:31:16.0 | 59.6 ± 7.3 | Schlieder et al. (2012a) | 2 |
| 2MASS J03445673–1145126 | 03:44:56.73 | –11:45:12.6 | 31.3 |
Gagné et al. (2015) | 2 |
| HD 232862 AB | 03:57:19.99 | +50:51:18.6 | 51.7 ± 5.7 | Schlieder et al. (2012a) | 2 |
| 1RXS J041137.6+250413 | 04:11:36.38 | +25:04:41.8 | 64.2 ± 9.0 | Schlieder et al. (2012a) | 2 |
| c Eri A | 04:37:36.13 | –02:28:24.8 | 29.43 ± 0.29 | van Leeuwen (2007) | 1 |
| c Eri Ca,Cb | 04:37:37.47 | –02:29:28.4 | 29.43 ± 0.29 | van Leeuwen (2007) | 1 |
| 2MUCD 10320 | 04:43:37.61 | +00:02:05.2 | 25.7 |
Gagné et al. (2014) | 2 |
| V962 Per | 04:43:56.87 | +37:23:03.3 | 59 ± 5 | Malo et al. (2014b) | 2 |
| LDS 5606 A | 04:48:00.86 | +14:39:58.1 | 65 ± 6 | Rodríguez et al. (2014) | 2 |
| LDS 5606 B | 04:48:02.58 | +14:39:51.6 | 65 ± 6 | Rodríguez et al. (2014) | 2 |
| V1005 Ori | 04:59:34.83 | +01:47:00.7 | 25.9 ± 1.7 | van Leeuwen (2007) | 1 |
| CD–57 1054 | 05:00:47.15 | –57:15:25.6 | 26.78 ± 0.81 | van Leeuwen (2007) | 1 |
| V1841 Ori | 05:00:49.29 | +15:27:00.7 | 53.8 ± 7.5 | Schlieder et al. (2012a) | 2 |
| 1RXS J050156.7+010845 | 05:01:56.66 | +01:08:42.9 | 27.0 ± 3.2 | Schlieder et al. (2012b) | 2 |
| LP 476–207 ABC | 05:01:58.81 | +09:58:58.8 | 24.6 ± 1.3 | Riedel et al. (2014) | 1 |
| TYC 693–948–1 | 05:02:47.84 | +12:22:56.4 | 66.8 ± 11.9 | Schlieder et al. (2012a) | 2 |
| RX J0506.2+0439 | 05:06:12.93 | +04:39:27.2 | 41.8 ± 6.0 | Schlieder et al. (2012a) | 2 |
| BD–21 1074Ba,Bb | 05:06:49.47 | –21:35:03.8 | 19.2 ± 0.5 | Riedel et al. (2014) | 1 |
| BD–21 1074A | 05:06:49.92 | –21:35:09.2 | 18.3 ± 0.7 | Riedel et al. (2014) | 1 |
| 1RXS J050712.4+143024 | 05:07:11.37 | +14:30:01.4 | 51.2 ± 7.0 | Schlieder et al. (2012a) | 2 |
| 1RXS J050827.3-210130 | 05:08:27.29 | –21:01:44.4 | 25 ± 5 | Malo et al. (2014b) | 2 |
| 1RXS J051954.1+315944 | 05:19:53.18 | +31:59:33.9 | 48.4 ± 5.2 | Schlieder et al. (2012a) | 2 |
| TYC 112–917–1 | 05:20:00.29 | +06:13:03.6 | 68.5 | Elliott et al. (2014) | 2 |
| 2E 1249 AB | 05:20:31.83 | +06:16:11.5 | 69.7 | Elliott et al. (2014) | 2 |
| CD–39 1935 | 05:22:45.69 | –39:17:06.1 | 33 ± 6 | Malo et al. (2013) | 2 |
| 1RXS J052419.1–160117 AB | 05:24:19.14 | –16:01:15.3 | 20 ± 5 | Malo et al. (2014b) | 2 |
| AF Lep AB | 05:27:04.77 | –11:54:03.3 | 27.04 ± 0.35 | van Leeuwen (2007) | 1 |
| 2E 1287 | 05:29:44.68 | –32:39:14.2 | 26.18 ± 1.10 | Riedel et al. (2014) | 2 |
| V1311 Ori AB | 05:32:04.50 | –03:05:29.2 | 42 ± 6 | Malo et al. (2013) | 1 |
| RBS 661 | 05:33:28.03 | –42:57:20.5 | 16 ± 4 | Malo et al. (2013) | 2 |
| RX J0534.0–0221 | 05:33:59.81 | –02:21:32.5 | 42 ± 5 | Malo et al. (2014b) | 2 |
| 1RXS J054223.7–275803 | 05:42:23.87 | –27:58:03.1 | 44 ± 9 | Malo et al. (2013) | 2 |
| β Pic | 05:47:17.08 | –51:03:59.5 | 19.44 ± 0.04 | van Leeuwen (2007) | 1 |
| 2MASS J06085283–2753583 | 06:08:52.83 | –27:53:58.3 | 31.269± 3.55 | Faherty et al. (2012) | 2 |
| 1RXS J061313.2–274205 AB | 06:13:13.30 | –27:42:05.4 | 29.4 ± 0.9 | Riedel et al. (2014) | 1 |
| TYC 6513–1245–1 | 06:13:57.75 | –27:23:55.3 | 51 ± 8 | Malo et al. (2013) | 2 |
| 1RXS J061610.6–132046 AB | 06:16:10.33 | –13:20:42.3 | 47 ± 7 | Malo et al. (2013) | 2 |
| AO Men | 06:18:28.24 | –72:02:41.6 | 38.55 ± 0.13 | van Leeuwen (2007) | 1 |
| 1RXS J065940.5+054541 | 06:59:41.57 | +05:45:40.0 | 44.3 ± 6.5 | Schlieder et al. (2012a) | 2 |
| LP 58–170 | 07:23:29.41 | +66:46:44.3 | 139.28 ± 42.48 | van Leeuwen (2007) | 2 |
| 1RXS J072643.1+185026 | 07:26:41.54 | +18:50:34.7 | 57.7 ± 8.1 | Schlieder et al. (2012a) | 2 |
| 1RXS J072931.4+355607 AB | 07:29:31.09 | +35:56:00.4 | 42.2 ± 4.0 | Schlieder et al. (2012b) | 2 |
| YZ CMi AB | 07:44:40.17 | +03:33:08.8 | 5.96 ± 0.08 | van Leeuwen (2007) | 2 |
| 2MASS J08025781–830076 | 08:02:57.81 | –83:30:07.6 | 20.5 |
Gagné et al. (2015) | 2 |
| EUVE J0817–82.7 AB | 08:17:39.44 | –82:43:29.8 | 27 ± 2 | Malo et al. (2014a) | 2 |
| L 186–67 Aa,Ab | 08:22:47.45 | –57:26:53.0 | 11.1 ± 3.3 | Lépine & Gaidos (2011) | 3 |
| 2MASS J08224748+0757171 | 08:22:47.49 | +07:57:17.2 | 62.4 ± 9.8 | Schlieder et al. (2012b) | 2 |
| [SLS2012] PYC J08290+1125 | 08:29:04.12 | +11:25:05.4 | 58.8 ± 8.5 | Schlieder et al. (2012a) | 2 |
| HD 73018 AB | 08:37:39.24 | +41:48:02.3 | 51.9 ± 5.7 | Schlieder et al. (2012a) | 2 |
| [SLS2012] PYC J09226+7122S | 09:22:37.64 | +71:22:07.3 | 65.9 ± 9.6 | Schlieder et al. (2012a) | 2 |
| HD 82939 Ba,Bb | 09:36:15.91 | +37:31:45.5 | 33.75 ± 2.61 | van Leeuwen (2007) | 3 |
| RX J1002.0+6651 | 10:01:59.95 | +66:51:27.7 | 38.7 ± 4.0 | Schlieder et al. (2012b) | 3 |
| DK Leo AB | 10:14:19.18 | +21:04:29.5 | 23.08 ± 0.96 | van Leeuwen (2007) | 2 |
| TWA 22 Aa,Ab | 10:17:26.89 | –53:54:26.5 | 17.5 ± 0.2 | Malo et al. (2014b) | 1 |
| [SLS2012] PYCJ10175+5542 | 10:17:31.43 | +55:42:29.4 | 63.0 ± 8.3 | Schlieder et al. (2012a) | 2 |
| RX J1035.9+2853 | 10:35:57.25 | +28:53:31.7 | 37.8 ± 3.9 | Schlieder et al. (2012b) | 2 |
| HD 95174 A | 10:59:38.31 | +25:26:15.5 | 22.6 ± 2.0 | Schlieder et al. (2012b) | 2 |
| HD 95174 B | 10:59:38.68 | +25:26:13.7 | 22.6 ± 2.0 | Schlieder et al. (2012b) | 2 |
| [SLS2012] PYC J11167+3814 | 11:16:46.09 | +38:14:13.6 | 67.6 ± 9.6 | Schlieder et al. (2012a) | 2 |
| RBS 1043 Aa,Ab,B | 11:51:56.81 | +07:31:26.3 | 33.2 ± 2.7 | Schlieder et al. (2012a) | 2 |
| 2E 2613 | 12:11:53.09 | +12:49:13.5 | 62.7 ± 8.2 | Schlieder et al. (2012a) | 2 |
| 1RXS J135452.3–712157 | 13:54:53.90 | –71:21:47.7 | 21 ± 1 | Malo et al. (2014a) | 3 |
| TYC 4634–1184–1 | 14:12:49.93 | +84:01:31.2 | 57.9 ± 9.7 | Schlieder et al. (2012a) | 2 |
| MV Vir Aa,Ab,B | 14:14:21.36 | –15:21:21.7 | 30.2 ± 4.5 | van Leeuwen (2007) | 2 |
| SCR J1425–4113 AB | 14:25:29.13 | –41:13:32.4 | 66.9 ± 4.3 | Riedel et al. (2014) | 3 |
| StKM 1–1155 | 14:25:55.93 | +14:12:10.1 | 51.8 ± 7.3 | Schlieder et al. (2012a) | 2 |
| α Cir AB | 14:42:30.42 | –64:58:30.5 | 16.57 ± 0.03 | van Leeuwen (2007) | 3 |
| V343 Nor B | 15:38:56.79 | –57:42:19.0 | 38.54 ± 1.69 | van Leeuwen (2007) | 1 |
| V343 Nor A | 15:38:57.57 | –57:42:27.3 | 38.54 ± 1.69 | van Leeuwen (2007) | 1 |
| TYC 4571–1414–1 | 16:17:11.48 | +77:33:47.8 | 65.0 ± 13.5 | Schlieder et al. (2012a) | 3 |
| d Sco | 16:18:17.90 | –28:36:50.5 | 41.29 ± 0.38 | van Leeuwen (2007) | 1 |
| 1RXS J164302.3–175418 | 16:43:01.28 | –17:54:27.4 | 59.2 ± 2.8 | Binks & Jeffries (2013) | 2 |
| 1RXS J165719.9–534328 | 16:57:20.30 | –53:43:31.7 | 51 ± 3 | Malo et al. (2014a) | 2 |
| 1RXS J171502.4–333344 | 17:15:02.20 | –33:33:39.8 | 23 ± 1 | Malo et al. (2014a) | 2 |
| CD–27 11535 Aa,Ab,B | 17:15:03.61 | –27:49:39.7 | 84.1 | Elliott et al. (2014) | 2 |
| V824 Ara Aa,Ab | 17:17:25.51 | –66:57:03.9 | 31.45 ± 4.94 | van Leeuwen (2007) | 1 |
| V824 Ara B | 17:17:31.29 | –66:57:05.6 | 31.45 ± 4.94 | van Leeuwen (2007) | 1 |
| 1RXS J172919.1–501454 AB | 17:29:20.67 | –50:14:52.9 | 64 ± 5 | Malo et al. (2014a) | 1 |
| CD–54 7336 | 17:29:55.07 | –54:15:48.8 | 66 | McCarthy & White (2012) | 1 |
| HD 160305 | 17:41:49.03 | –50:43:27.9 | 72.46 ± 4.57 | van Leeuwen (2007) | 1 |
| HD 161460 AB | 17:48:33.74 | –53:06:43.3 | 69.8 | Elliott et al. (2014) | 1 |
| HD 164249 AB | 18:03:03.41 | –51:38:56.4 | 48.15 ± 1.30 | van Leeuwen (2007) | 1 |
| HD 165189 AB | 18:06:49.90 | –43:25:30.8 | 41.84 ± 1.16 | van Leeuwen (2007) | 1 |
| V4046 Sgr AB | 18:14:10.48 | –32:47:34.4 | 73 ± 18 | Kastner et al. (2011) | 1 |
| V4046 Sgr C | 18:14:22.07 | –32:46:10.1 | 73 ± 18 | Kastner et al. (2011) | 1 |
| 1RXS J181514.7–492755 | 18:15:15.64 | –49:27:47.2 | 61 ± 4 | Malo et al. (2014a) | 2 |
| HD 168210 | 18:19:52.21 | –29:16:32.8 | 72.57 ± 5.37 | van Leeuwen (2007) | 1 |
| FK Ser AB | 18:20:22.75 | –10:11:13.6 | 75.93 ± 22.00 | van Leeuwen (2007) | 3 |
| 1RXS J184206.5–555426 | 18:42:06.95 | –55:54:25.5 | 54 ± 4 | Malo et al. (2014a) | 2 |
| HD 172555 A | 18:45:26.91 | –64:52:16.5 | 28.55 ± 0.16 | van Leeuwen (2007) | 1 |
| HD 172555 Ba,Bb | 18:45:37.05 | –64:51:46.1 | 29.24 ± 0.60 | van Leeuwen (2007) | 1 |
| Smethells 20 (HD 173167 B) | 18:46:52.56 | –62:10:36.7 | 54 ± 3 | Malo et al. (2014a) | 1 |
| HD 173167 A | 18:48:06.36 | –62:13:47.0 | 52 | Holmberg et al (2009) | 2 |
| 1RXS J184956.1-013402 | 18:49:55.44 | –01:34:08.7 | 23 ± 6 | Malo et al. (2014b) | 3 |
| CD–31 16041 | 18:50:44.48 | –31:47:47.2 | 53 ± 3 | Malo et al. (2014a) | 1 |
| PZ Tel Aa,Ab | 18:53:05.87 | –50:10:50.0 | 51.49 ± 2.60 | van Leeuwen (2007) | 1 |
| TYC 6872–1011–1 | 18:58:04.15 | –29:53:04.6 | 76 ± 5 | Malo et al. (2014b) | 1 |
| 2MASS J18580464–2953320 | 18:58:04.66 | –29:53:32.2 | 76 ± 5 | Malo et al. (2014b) | 1 |
| 1RXS J191028.6-231934 | 19:10:28.20 | –23:19:48.6 | 67 ± 5 | Malo et al. (2014b) | 2 |
| CD–26 13904 AB | 19:11:44.68 | –26:04:08.5 | 80 | McCarthy & White (2012) | 1 |
| η Tel AB | 19:22:51.22 | –54:25:26.3 | 48.22 ± 0.49 | van Leeuwen (2007) | 1 |
| η Tel C | 19:22:58.95 | –54:32:17.1 | 51.81 ± 1.74 | van Leeuwen (2007) | 1 |
| 1RXS J192338.2–460631 | 19:23:38.20 | –46:06:31.6 | 70 ± 4 | Malo et al. (2014b) | 2 |
| RX J1924.5-3442 | 19:24:34.95 | –34:42:39.3 | 54 ± 3 | Malo et al. (2014a) | 2 |
| 2MASS J19395435–5216468 | 19:39:54.35 | –52:16:46.8 | 28.9 |
Gagné et al. (2015) | 2 |
| HDE 331149 A | 19:43:37.90 | +32:25:12.5 | 37.6 ± 8.3 | Schlieder et al. (2012a) | 2 |
| 2MASS J19444417–4359015 | 19:44:44.17 | –43:59:01.5 | 28.1 ± 2.4 | Gagné et al. (2015) | 2 |
| 1RXS J195602.8–320720 AB | 19:56:02.94 | –32:07:18.7 | 55 ± 4 | Malo et al. (2014a) | 1 |
| TYC 7443–1102–1 | 19:56:04.38 | –32:07:37.6 | 55 ± 3 | Malo et al. (2014a) | 1 |
| 2MASS J20004841–7523070 | 20:00:48.42 | –75:23:07.0 | 33.3 |
Gagné et al. (2014) | 2 |
| 1RXS J200136.9–331307 | 20:01:37.18 | –33:13:14.0 | 61 ± 4 | Malo et al. (2014a) | 2 |
| HD 191089 | 20:09:05.22 | –26:13:26.5 | 52.22 ± 1.23 | van Leeuwen (2007) | 1 |
| 1RXS J201001.0–280139 AB | 20:10:00.02 | –28:01:41.0 | 48.0 ± 3.1 | Riedel et al. (2014) | 1 |
| SCR J2033-4903 | 20:33:01.86 | –49:03:10.5 | 16.3 ± 5.0 | Gagné et al. (2015) | 2 |
| 1RXS J203336.9-255654 | 20:33:37.59 | –25:56:52.1 | 48.3 ± 3.3 | Riedel et al. (2014) | 1 |
| 2MASS J20334670–3733443 | 20:33:46.70 | –37:33:44.3 | 33.8 ± 2.8 | Gagné et al. (2015) | 2 |
| AU Mic BC (AT Mic AB) | 20:41:51.12 | –32:26:07.3 | 10.70 ± 0.42 | van Leeuwen (2007) | 1 |
| StHA 182 AB | 20:43:41.14 | –24:33:53.4 | 28.1 ± 3.9 | Shkolnik et al. (2012) | 2 |
| AU Mic | 20:45:09.49 | –31:20:26.7 | 9.91 ± 0.10 | van Leeuwen (2007) | 1 |
| 2MASS J20513567+1924020 | 20:51:35.68 | +19:24:02.0 | 51.0 ± 8.0 | Schlieder et al. (2012a) | 2 |
| HD 199143 AB | 20:55:47.68 | –17:06:51.0 | 45.66 ± 1.60 | van Leeuwen (2007) | 1 |
| HD 199143 CD (AZ Cap AB) | 20:56:02.75 | –17:10:53.9 | 45.66 ± 1.60 | van Leeuwen (2007) | 1 |
| 1RXS J210736.5–130500 | 21:07:36.79 | –13:04:58.2 | 36 ± 2 | Malo et al. (2013) | 3 |
| EUVE J2110–19.3 | 21:10:05.36 | –19:19:57.4 | 32 ± 2 | Malo et al. (2014b) | 2 |
| 2MASS J21103096–2710513 | 21:10:30.96 | –27:10:51.3 | 40 ± 2 | Malo et al. (2013) | 2 |
| 2MASS J21103147–2710578 | 21:10:31.48 | –27:10:57.8 | 41 ± 3 | Malo et al. (2014b) | 2 |
| 2MASS J21140802–2251358 | 21:14:08.03 | –22:51:35.8 | 22.1 ± 1.6 | Gagné et al. (2014) | 2 |
| StKM 1–1877 | 21:18:33.76 | +30:14:34.6 | 50.5 ± 8.0 | Schlieder et al. (2012b) | 2 |
| V390 Pav A | 21:21:24.49 | –66:54:57.4 | 30.2 ± 1.3 | van Leeuwen (2007) | 3 |
| V390 Pav B | 21:21:28.72 | –66:55:06.3 | 30.2 ± 1.3 | van Leeuwen (2007) | 3 |
| 2E 4498 AB | 21:37:40.19 | +01:37:13.7 | 39.2 ± 4.0 | Schlieder et al. (2012b) | 2 |
| 1RXS J214127.5+204302 | 21:41:26.62 | +20:43:10.7 | 57.2 ± 8.5 | Schlieder et al. (2012a) | 2 |
| 1RXS J215518.2–004603 | 21:55:17.41 | –00:45:47.8 | 47 ± 4 | Malo et al. (2013) | 2 |
| RX J2155.3+5938 AB | 21:55:24.36 | +59:38:37.1 | 29.9 ± 4.1 | Schlieder et al. (2012a) | 2 |
| RX J2200.7+2715 | 22:00:41.58 | +27:15:13.5 | 44 ± 4 | Malo et al. (2013) | 1 |
| LSPM J2240+0532 | 22:40:01.45 | +05:32:16.3 | 23.6 ± 2.7 | Gagné et al. (2015) | 2 |
| CPD–72 2713 | 22:42:48.96 | –71:42:21.1 | 37 ± 2 | Malo et al. (2014a) | 1 |
| WW PsA A | 22:44:57.94 | –33:15:01.6 | 23.34 ± 1.97 | van Leeuwen (2007) | 1 |
| WW PsA B (TX PsA) | 22:45:00.05 | –33:15:25.8 | 23.34 ± 1.97 | van Leeuwen (2007) | 1 |
| 1RXS J225710.4+363950 | 22:57:11.31 | +36:39:45.2 | 68.7 ± 11.4 | Schlieder et al. (2012b) | 2 |
| LP 462–19 AB | 23:17:28.07 | +19:36:46.9 | 12 ± 1 | Malo et al. (2013) | 2 |
| AF Psc | 23:31:44.93 | –02:44:39.6 | 29.15 ± 2.64 | van Altena et al. (1995) | 3 |
| BD–13 6424 | 23:32:30.85 | –12:15:51.3 | 28 ± 1 | Malo et al. (2014a) | 1 |
| 2E 4766 | 23:50:06.39 | +26:59:51.9 | 24 ± 2 | Malo et al. (2014a) | 3 |
| G 68–46 | 23:51:22.28 | +23:44:20.8 | 16 ± 1 | Malo et al. (2014a) | 3 |
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