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Spot test (lichen)

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738: 633: 120: 332: 353:(PD), made by placing a drop of ethanol (70–95%) over a few crystals of the chemical; this yields an unstable, light sensitive solution that lasts for about a day. An alternative form of this solution, called Steiner's solution, is much longer lasting although it produces less intense colour reactions. It is typically prepared by dissolving 1 gram of PD, 10 grams of 267:. These solutions are typically replaced daily since they break down within 24–48 hours; they break down even more rapidly when exposed to sunlight (less than an hour) and so are recommended to keep in a dark-coloured bottle. Other factors that accelerate the decomposition of these solutions are heat, humidity, and 692:
is used to try to make the colour reaction more readily observable. The lichen fragment is pressed on the paper, and lichen substances are extracted with 10–20 drops of acetone. After evaporating the acetone, the lichen substances are left on the paper in a ring around the lichen fragment. The filter
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can take up to half a minute. In contrast, the reactions with C and KC are usually fleeting and occur within a second of applying the reagent, so a colour change can easily be missed. There are several possible reasons that an anticipated test result does not occur. Causes include old and chemically
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Products of this reaction are yellow to red in colour. Most β-orcinol depsidones and some β-orcinol depsides will react positively. The PD test, known for its high specificity towards substances that yield K+ yellow or red reactions, has largely replaced the simpler yet less conclusive K test. PD is
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Spot tests may be used individually or in combination. The results of a spot tests are typically represented with a short code that includes, in order, (1) a letter indicating the reagent used, (2) a "+" or "−" sign indicating a colour change or lack of colour change, respectively, and (3) a letter
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is generally considered to have been the first to demonstrate the use of chemicals to help with lichen identification. In papers published in 1866, he suggested spot tests using KOH and bleaching powder to get characteristic colour reactions—typically yellow, red, or green. In these studies he
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solution (P test). The colour changes occur due to presence of particular secondary metabolites in the lichen. In identification key reference literature, the outcome of chemical spot tests serves as a primary characteristic for determining the species of lichens. There are several other less
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because the presence of parietin in the former species results in a strong colour reaction. He also knew that in some cases the lichen chemicals were not evenly distributed throughout the cortex and the medulla due to the differing colour reactions on these areas. In the mid-1930s,
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or word indicating the colour observed. In addition, care should be taken to indicate which part of the lichen was tested. For example, "Cortex K+ orange, C−, P−" means the cortex of the test specimen turned orange with application of KOH and did not change under bleach or
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There are several spot tests that are infrequently used due to their limited applicability, but may be useful in situations where particular lichen metabolites need to be detected, or to distinguish between certain species when other tests are negative.
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such that exposing certain parts of the lichen to a UV light source can reveal the presence or absence of those metabolites similarly to spot tests. Examples of lichen substances that give a bright fluorescence in UV are alectoronic,
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inactive reagents, and low concentrations of lichen substances in the sample. If the colour of the thallus is dark, a colour change might be obscured, and other techniques are more appropriate, like the filter paper technique.
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could be distinguished as distinct species due to their different colour reactions: C+ red in the latter, contrasted with no reaction in the former. Nylander showed how KOH could be used to distinguish between the lookalikes
165:(NaOH, lye), which provides nearly identical results. A 10% solution of KOH will retain its effectiveness for about 6 months to a year. The test depends on salt formation and requires the presence of at least one acidic 715:-phenylenediamine. Similarly, "Medulla K−, KC+R" would indicate the medulla of the lichen was insensitive to application of KOH, but application of KOH followed immediately by bleach caused the medulla to turn red. 858:-phenylendiamine, which gives yellow to red reactions with secondary metabolites that have a free aldehyde group. This spot test was later shown to be particularly useful in the taxonomy of the family 681:
blade may be used to remove the cortex and access the medulla. Alternatively, the solution can be applied to lichen features that lack a cortex or that leave the medulla exposed, such as soralia,
588:-extracted, dried sample from a lichen thallus, followed by heating over a flame for 30 seconds or until colour develops. A persistent violet to bright pink colour indicates the presence of 68:. As such, spot tests reveal the presence or absence of chemicals in various parts of a lichen. They were first proposed as a method to help identify species by the Finnish lichenologist 469:
is present. The CK test is a less commonly used variation that reverses the order of the application of chemicals. It is used in special cases when testing for orange colour produced by
103:, accommodate different lichen types and pigmentations, with results typically summarised by a short code indicating the substance and reaction observed. Other diagnostic methods like 95:
frequently used spot tests of more limited use that are employed in specific situations, such as to distinguish between certain species. Variations of the technique, including using
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paper can then be spot tested in the usual way. In cases where the results of a spot test on the thallus are uncertain, it is possible to squash a thin section of the tissue on a
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in 100 millilitres of water; initially pink in colour, the solution becomes purple with age. Steiner's solution will last for months. The phenylenediamine reacts with
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on different parts of the lichen and noting the colour change (or lack thereof) associated with application of the chemical. The tests are routinely encountered in
804: 286:, while those resulting in orange-red include gyrophoric acid. Rarely, an emerald-green colour is produced, caused by reaction with dihydroxy 1646: 1594: 1166: 1106: 1008: 133:
showing thallus (top) and medulla (bottom). The pinkish-red colour change of the medulla in the C and KC tests indicate the presence of
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Spot tests are performed by placing a small amount of the desired reagent on the portion of the lichen to be tested. Often, both the
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Asahina, Y. (1936). "Mikrochemischer Nachweis der Flechtenstoffe (I)" [Microchemical detection of lichen substances (I)].
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Le Pogam, Pierre; Herbette, Gaëtan; Boustie, Joël (19 December 2014). "Analysis of Lichen Metabolites, a Variety of Approaches".
701:, or when the slide placed against a white background. This technique is useful when testing lichens with dark pigments, such as 759:
It may sometimes be useful to perform other diagnostic measures in addition to spot tests. For example, some lichen metabolites
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and touch it to the lichen thallus; a small paint brush is also used for this purpose. Reactions are best visualised with a
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Nylander, William (November 1866). "Hypochlorite of lime and hydrate of potash, two new criteria in the study of lichens".
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may also be useful in initially characterising the chemical composition of lichens or when spot tests are unrevealing.
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poisonous both as a powder and a solution, and surfaces that come in contact with it (including skin) will discolour.
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in a minimal amount of water and reagent under a cover slip. A colour change is visible under a low-power microscope
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Asahina, Y. (1934). "Über die Reaktion vom Flechten-Thallus" [About the response from the lichen thallus].
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Colours typically observed with the C test are red and orange-rose. Chemicals causing a red reaction include
107:(UV) light exposure can help identify lichen metabolites and distinguish between species, as some substances 1665: 780:. In some cases, the UV light test can be used to help distinguish between closely related species, such as 415:
Some common and widely distributed lichens that have lichen products with a positive reaction to P include
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Some common and widely distributed lichens that have lichen products with a positive reaction to C include
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Some common and widely distributed lichens that have lichen products with a positive reaction to K include
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as part of their structure will produce a dark red to violet colour. Example compounds include the
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In a variation of this technique, suggested by the Swedish chemist Johan Santesson, a piece of
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Occasionally, it takes some time for the colour reaction to develop. For example, in certain
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Alphandary, Elisa; McCune, Bruce (2013). "A new chemical spot test for miriquidic acid".
137:, a chemical feature that helps to distinguish it from similar species in the same genus. 1069:"A revised guide to microchemical techniques for the identification of lichen products" 906: 612: 581: 573: 354: 283: 268: 198: 182: 124: 57: 1659: 921: 777: 661:
of the lichen are tested, and at times it is useful to test other structures such as
528: 470: 213: 178: 41: 1389: 1331: 1068: 259:(bleaching powder), or alternatively a dilute solution (5.25% is typically used) of 947: 859: 760: 689: 287: 275: 96: 331: 1548:
Torrey, Raymond H. (1935). "Paraphenylenediamine, a new color test for lichens".
1488: 1465: 1098: 17: 1630: 1608: 1312:"Chemical studies on lichens. 4. Thin layer chromatography of lichen substances" 1221: 616: 593: 562: 439:
with K followed immediately by C. The initial application of K breaks down (via
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is a lichen that is KC+ (orange-pink) because of the depsidone physodic acid;
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to another hydroxyl, then a red to orange colour is produced as C is applied.
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Four spot tests are used most commonly to help with lichen identification.
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and can be used to distinguish between the two morphologically similar
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is another reagent that may be useful in identifying certain species.
1491:[New criteria to be added to the chemical study of lichens]. 796:). Only long-wavelength UV is useful for observing lichens directly. 448: 161:(KOH) (10–25%), or, in the absence of KOH, a 10% aqueous solution of 45: 1375: 111:
under UV, aiding in the differentiation of closely related species.
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involves heating a small sample of the substance to be tested on a
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for lichen species, and they take advantage of the wide array of
421:, which is PD+ (yellow) because of the didepside atranorin, and 65: 1263: 1261: 1232:. New Haven, Conn. : Yale University Press. pp. 103–108. 973: 971: 189:. Yellow to red colours are produced with the K test and some 1489:"Quaedam addenda ad nova criteria chemica in studio lichenum" 608:
without having to resort to more laborious chemical analysis.
1468:[A new chemical criterion in the study of lichen]. 1440:
10.1639/0007-2745(2001)104[0263:WNALC]2.0.CO;2
1293: 1291: 1180: 1178: 1161:(2nd ed.). London: Edward Arnold. pp. 119–121. 1062: 1060: 1058: 1056: 1054: 1052: 501:
is KC+ (pink-red) due to the depsidone alectoronic acid.
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produce this colour, while a violet colour results when
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to enhance visibility of reactions or examining under a
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Microchemical Methods for the Identification of Lichens
1424:"William Nylander (1822–1899) and lichen chemotaxonomy" 1390:"Arizona State University Lichen Herbarium: Lichen TLC" 1084: 1082: 1003:. New Haven: Yale University Press. pp. 369–371. 1358:
Brodo, Irwin M. (1991). "Studies in the lichen genus
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compounds cause a temporary deep green flame colour.
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Macrolichens of Denmark, Finland, Norway and Sweden
1466:"Circa novum in studio lichenum criterium chemicum" 824:showed, for example, that the lichens now known as 1414: 1412: 1410: 48:. It is performed by placing a drop of a chemical 342:This is also known as the P test. It uses a 1–5% 169:in the molecule. Lichen compounds that contain a 79:solution (K test), saturated aqueous solution of 64:) produced by lichens and their uniqueness among 1252: 1196: 1126: 1031: 895:Journal of the Linnean Society of London, Botany 888: 886: 1093:. New Delhi: Springer India. pp. 229–261. 994: 992: 990: 988: 986: 435:This spot test may be performed by wetting the 309:, which is C+ (orange) because of the xanthone 75:Three common spot tests use either 10% aqueous 926:group (lichenized ascomycetes) in Switzerland" 565:, which can be used to distinguish species of 1345: 1208: 1141: 1043: 977: 799:More advanced analytical techniques, such as 319:, which is C+ (red) because of the didepside 29:A chemical test used to help identify lichens 8: 1362:. 2. Corticolous species of North America". 1152: 1150: 300:as a result of the dibenzofuran usnic acid. 1330: 920:Truong, Camille; Clerc, Philippe (2003). 522:) gives a violet colour when tested with 1297: 1184: 403: 399: 395: 391: 387: 383: 379: 375: 882: 584:solution (0.5% to 10%) brushed over an 255:This test uses a saturated solution of 1073:Bulletin of the British Lichen Society 1067:Walker, F.J.; James, P.W. (May 1980). 805:high-performance liquid chromatography 229:, which is K+ (red-purple) due to the 952:Macrolichens of the Pacific Northwest 550:A 1% (weight per volume) solution of 369:according to the following reaction: 7: 1001:A Field Guide to California Lichens 451:hydroxyl group is released that is 239:, which is K+ (yellow), due to the 907:10.1111/j.1095-8339.1866.tb01301.x 561:The N test uses a 35% solution of 25: 685:, or the underside of squamules. 447:in depsides and depsidones. If a 1332:10.3891/acta.chem.scand.21-1162 1531:The Journal of Japanese Botany 1253:Orange, James & White 2001 1197:Orange, James & White 2001 1127:Orange, James & White 2001 1091:Recent Advances in Lichenology 1032:Orange, James & White 2001 724:species, the PD reaction with 1: 1589:. New York: Academic Press. 1099:10.1007/978-81-322-2181-4_11 636:Chemical spot tests on the 526:, a chemical found in some 1687: 1641:. British Lichen Society. 1364:Canadian Journal of Botany 1310:Santesson, Johann (1967). 1224:; Sharnoff, Sylvia Duran; 999:Sharnoff, Stephen (2014). 220:do not have any reaction. 87:(C test), or 5% alcoholic 1346:Ahmadjian & Hale 1973 1319:Acta Chemica Scandinavica 1282:10.1017/s0024282913000418 1209:Ahmadjian & Hale 1973 1142:Ahmadjian & Hale 1973 1075:. 46 (Supplement): 13–29. 1044:Ahmadjian & Hale 1973 978:Ahmadjian & Hale 1973 801:thin-layer chromatography 792:(UV+, due to presence of 357:, and 0.5 millilitres of 1615:. Universitetsforlaget. 1230:Lichens of North America 950:; Geiser, Linda (1997). 535:A saturated solution of 477:, such as is present in 233:(an anthraquinone), and 749:of the crustose lichen 726:fumarprotocetraric acid 290:, such as the chemical 1637:; White, F.J. (2001). 1159:The Biology of Lichens 854:created the test with 819:Finnish lichenologist 756: 650: 571:from brown species of 339: 316:Diploschistes muscorum 138: 44:used to help identify 1487:Nylander, W. (1866). 827:Cetrelia cetrarioides 765:ultraviolet radiation 740: 635: 628:Performing spot tests 605:S. groenlandicum 334: 153:for the K test is an 122: 62:secondary metabolites 1298:Dahl & Krog 1973 1185:Dahl & Krog 1973 1157:Hale, Mason (1974). 872:Microcrystallization 840:Xanthoria candelaria 752:Ochrolechia africana 599:Stereocaulon alpinum 543:), when tested with 524:diploschistesic acid 321:diploschistesic acid 257:calcium hypochlorite 85:calcium hypochlorite 1144:, pp. 636–637. 846:Candelaria concolor 789:Cladonia sulphurina 647:Aspicilia epiglypta 498:Cetrelia olivetorum 492:Hypogymnia tubulosa 480:Cladonia floerkeana 424:Hypogymnia physodes 418:Parmelia subrudecta 297:Cladonia portentosa 261:sodium hypochlorite 226:Xanthoria parietina 159:potassium hydroxide 930:Botanica Helvetica 833:C. olivetorum 757: 651: 580:The S test uses a 514:A 10% solution of 467:picrolichenic acid 340: 306:Lecanora expallens 139: 123:Spot tests on the 1648:978-0-9540418-0-9 1596:978-0-12-044950-7 1579:Ahmadjian, Vernon 1512:Acta Phytochimica 1270:The Lichenologist 1226:Sharnoff, Stephen 1168:978-0-7131-2456-9 1108:978-81-322-2180-7 1010:978-0-300-19500-2 809:mass spectrometry 783:Cladonia deformis 774:divaricatic acids 675:stereo microscope 505:Less common tests 351:-phenylenediamine 338:-phenylenediamine 236:Dibaeis baeomyces 216:derivatives, and 187:terphenylquinones 130:Punctelia borreri 92:-phenylenediamine 18:Lichen spot tests 16:(Redirected from 1678: 1652: 1626: 1600: 1572:Cited literature 1566: 1565: 1545: 1539: 1538: 1526: 1520: 1519: 1507: 1501: 1500: 1484: 1478: 1477: 1458: 1452: 1451: 1420:Vitikainen, Orvo 1416: 1405: 1404: 1402: 1400: 1386: 1380: 1379: 1355: 1349: 1343: 1337: 1336: 1334: 1316: 1307: 1301: 1295: 1286: 1285: 1265: 1256: 1250: 1244: 1243: 1218: 1212: 1206: 1200: 1194: 1188: 1182: 1173: 1172: 1154: 1145: 1139: 1130: 1124: 1113: 1112: 1086: 1077: 1076: 1064: 1047: 1041: 1035: 1029: 1023: 1022: 996: 981: 975: 966: 965: 944: 938: 937: 924:Parmelia borreri 917: 911: 910: 890: 852:Yasuhiko Asahina 821:William Nylander 695:microscope slide 516:barium hydroxide 475:diffractaic acid 459:Alectoronic acid 407: 265:household bleach 245:baeomycesic acid 167:functional group 163:sodium hydroxide 155:aqueous solution 81:bleaching powder 70:William Nylander 54:dichotomous keys 21: 1686: 1685: 1681: 1680: 1679: 1677: 1676: 1675: 1656: 1655: 1649: 1629: 1623: 1603: 1597: 1577: 1574: 1569: 1547: 1546: 1542: 1528: 1527: 1523: 1509: 1508: 1504: 1486: 1485: 1481: 1460: 1459: 1455: 1418: 1417: 1408: 1398: 1396: 1388: 1387: 1383: 1376:10.1139/b91-099 1357: 1356: 1352: 1344: 1340: 1314: 1309: 1308: 1304: 1296: 1289: 1267: 1266: 1259: 1251: 1247: 1240: 1222:Brodo, Irwin M. 1220: 1219: 1215: 1207: 1203: 1195: 1191: 1183: 1176: 1169: 1156: 1155: 1148: 1140: 1133: 1125: 1116: 1109: 1088: 1087: 1080: 1066: 1065: 1050: 1042: 1038: 1030: 1026: 1011: 998: 997: 984: 976: 969: 962: 946: 945: 941: 919: 918: 914: 901:(38): 358–365. 892: 891: 884: 880: 868: 817: 741:UV-illuminated 735: 683:pseudocyphellae 630: 590:miriquidic acid 557: 552:ferric chloride 545:olivetoric acid 542: 537:barium peroxide 521: 507: 433: 405: 401: 397: 393: 389: 385: 381: 377: 373: 329: 311:thiophanic acid 263:, or undiluted 253: 208:. In contrast, 183:naphthoquinones 147: 135:gyrophoric acid 117: 58:lichen products 30: 23: 22: 15: 12: 11: 5: 1684: 1682: 1674: 1673: 1668: 1666:Chemical tests 1658: 1657: 1654: 1653: 1647: 1627: 1621: 1601: 1595: 1583:Hale, Mason E. 1573: 1570: 1568: 1567: 1556:(4): 110–112. 1540: 1521: 1502: 1479: 1453: 1434:(2): 263–267. 1428:The Bryologist 1406: 1381: 1370:(4): 733–772. 1350: 1348:, p. 634. 1338: 1302: 1287: 1276:(5): 697–699. 1257: 1245: 1239:978-0300082494 1238: 1213: 1211:, p. 637. 1201: 1189: 1174: 1167: 1146: 1131: 1114: 1107: 1078: 1048: 1046:, p. 635. 1036: 1024: 1009: 982: 980:, p. 636. 967: 960: 939: 912: 881: 879: 876: 875: 874: 867: 864: 816: 813: 794:squamatic acid 734: 731: 629: 626: 625: 624: 613:Beilstein test 609: 582:sulphuric acid 578: 574:Xanthoparmelia 559: 555: 548: 540: 533: 519: 506: 503: 485:Lugol's iodine 432: 429: 409: 408: 355:sodium sulfite 328: 325: 284:lecanoric acid 269:carbon dioxide 252: 249: 201:), and many β- 199:thamnolic acid 179:anthraquinones 146: 143: 116: 113: 28: 24: 14: 13: 10: 9: 6: 4: 3: 2: 1683: 1672: 1669: 1667: 1664: 1663: 1661: 1650: 1644: 1640: 1636: 1632: 1628: 1624: 1622:9788200022626 1618: 1614: 1610: 1606: 1602: 1598: 1592: 1588: 1584: 1580: 1576: 1575: 1571: 1563: 1559: 1555: 1551: 1544: 1541: 1536: 1533:(in German). 1532: 1525: 1522: 1517: 1514:(in German). 1513: 1506: 1503: 1498: 1494: 1490: 1483: 1480: 1475: 1471: 1467: 1463: 1457: 1454: 1449: 1445: 1441: 1437: 1433: 1429: 1425: 1421: 1415: 1413: 1411: 1407: 1395: 1391: 1385: 1382: 1377: 1373: 1369: 1365: 1361: 1354: 1351: 1347: 1342: 1339: 1333: 1328: 1325:: 1162–1172. 1324: 1320: 1313: 1306: 1303: 1300:, p. 24. 1299: 1294: 1292: 1288: 1283: 1279: 1275: 1271: 1264: 1262: 1258: 1254: 1249: 1246: 1241: 1235: 1231: 1227: 1223: 1217: 1214: 1210: 1205: 1202: 1199:, p. 17. 1198: 1193: 1190: 1187:, p. 23. 1186: 1181: 1179: 1175: 1170: 1164: 1160: 1153: 1151: 1147: 1143: 1138: 1136: 1132: 1129:, p. 16. 1128: 1123: 1121: 1119: 1115: 1110: 1104: 1100: 1096: 1092: 1085: 1083: 1079: 1074: 1070: 1063: 1061: 1059: 1057: 1055: 1053: 1049: 1045: 1040: 1037: 1034:, p. 15. 1033: 1028: 1025: 1020: 1016: 1012: 1006: 1002: 995: 993: 991: 989: 987: 983: 979: 974: 972: 968: 963: 961:0-87071-394-9 957: 953: 949: 948:McCune, Bruce 943: 940: 935: 931: 927: 925: 916: 913: 908: 904: 900: 896: 889: 887: 883: 877: 873: 870: 869: 865: 863: 861: 857: 853: 848: 847: 842: 841: 835: 834: 829: 828: 822: 814: 812: 810: 806: 802: 797: 795: 791: 790: 785: 784: 779: 778:lichexanthone 775: 771: 766: 762: 754: 753: 748: 744: 739: 732: 730: 727: 723: 722: 716: 714: 708: 706: 705: 700: 696: 691: 686: 684: 680: 676: 672: 668: 664: 660: 656: 649: 648: 643: 639: 634: 627: 622: 618: 614: 610: 607: 606: 601: 600: 595: 591: 587: 583: 579: 576: 575: 570: 569: 564: 560: 553: 549: 546: 538: 534: 531: 530: 529:Diploschistes 525: 517: 513: 512: 511: 504: 502: 500: 499: 494: 493: 488: 486: 482: 481: 476: 472: 471:barbatic acid 468: 464: 463:physodic acid 460: 456: 455: 450: 446: 442: 438: 430: 428: 426: 425: 420: 419: 413: 372: 371: 370: 368: 364: 360: 356: 352: 350: 345: 337: 333: 326: 324: 322: 318: 317: 312: 308: 307: 301: 299: 298: 293: 289: 288:dibenzofurans 285: 281: 277: 272: 270: 266: 262: 258: 250: 248: 246: 242: 238: 237: 232: 228: 227: 221: 219: 215: 214:pulvinic acid 211: 207: 204: 200: 196: 192: 188: 184: 180: 176: 172: 168: 164: 160: 156: 152: 144: 142: 136: 132: 131: 126: 121: 114: 112: 110: 106: 102: 98: 93: 91: 86: 82: 78: 73: 71: 67: 63: 59: 55: 51: 47: 43: 42:spot analysis 39: 35: 27: 19: 1638: 1612: 1609:Krog, Hildur 1586: 1553: 1549: 1543: 1534: 1530: 1524: 1515: 1511: 1505: 1496: 1495:(in Latin). 1492: 1482: 1473: 1472:(in Latin). 1469: 1462:Nylander, W. 1456: 1431: 1427: 1399:18 September 1397:. Retrieved 1393: 1384: 1367: 1363: 1359: 1353: 1341: 1322: 1318: 1305: 1273: 1269: 1255:, p. 9. 1248: 1229: 1216: 1204: 1192: 1158: 1090: 1072: 1039: 1027: 1000: 951: 942: 933: 929: 923: 915: 898: 894: 860:Cladoniaceae 855: 844: 838: 831: 825: 818: 798: 787: 781: 758: 750: 719: 717: 712: 709: 702: 690:filter paper 687: 652: 645: 603: 597: 594:snow lichens 572: 566: 527: 508: 496: 490: 489: 478: 453: 434: 422: 416: 414: 410: 367:Schiff bases 348: 346:solution of 341: 335: 314: 304: 302: 295: 276:anziaic acid 273: 254: 234: 224: 222: 148: 140: 128: 97:filter paper 89: 74: 33: 31: 26: 1671:Lichenology 1635:James, P.W. 1605:Dahl, Eilif 1587:The Lichens 1394:nhc.asu.edu 1360:Ochrolechia 936:(1): 49–61. 733:Other tests 621:halogenated 617:copper wire 563:nitric acid 445:ester bonds 390:→ R−CH=N−C 193:(including 105:ultraviolet 38:lichenology 1660:Categories 1631:Orange, A. 1537:: 516–525. 1499:: 233–234. 1476:: 198–201. 878:References 786:(UV−) and 642:saxicolous 441:hydrolysis 292:strepsilin 218:usnic acid 206:depsidones 101:microscope 1019:862053107 761:fluoresce 747:apothecia 699:objective 671:hand lens 667:capillary 568:Melanelia 374:R−CHO + H 365:to yield 363:aldehydes 359:detergent 344:ethanolic 243:compound 241:didepside 210:xanthones 195:atranorin 177:that are 109:fluoresce 72:in 1866. 34:spot test 1611:(1973). 1585:(1973). 1562:40597010 1518:: 47–64. 1464:(1866). 1422:(2001). 1228:(2001). 866:See also 721:Cladonia 638:crustose 532:species. 449:phenolic 280:erythrin 231:parietin 191:depsides 175:pigments 1550:Torreya 1448:3244891 815:History 770:lobaric 743:thallus 704:Bryoria 663:soralia 659:medulla 644:lichen 586:acetone 518:(Ba(OH) 437:thallus 431:KC test 327:PD test 203:orcinol 171:quinone 151:reagent 127:lichen 125:foliose 50:reagent 46:lichens 1645:  1619:  1593:  1560:  1446:  1236:  1165:  1105:  1017:  1007:  958:  807:, and 776:, and 772:, and 763:under 655:cortex 313:, and 282:, and 251:C test 185:, and 145:K test 1558:JSTOR 1493:Flora 1470:Flora 1444:JSTOR 1315:(PDF) 922:"The 679:razor 673:or a 554:(FeCl 115:Tests 40:is a 1643:ISBN 1617:ISBN 1591:ISBN 1401:2016 1234:ISBN 1163:ISBN 1103:ISBN 1015:OCLC 1005:ISBN 956:ISBN 856:para 843:and 830:and 745:and 713:para 677:. A 657:and 640:and 611:The 602:and 539:(BaO 461:and 454:meta 349:para 197:and 149:The 66:taxa 1436:doi 1432:104 1372:doi 1327:doi 1278:doi 1095:doi 934:113 903:doi 473:or 402:+ H 398:−NH 386:−NH 378:N−C 157:of 83:or 77:KOH 36:in 1662:: 1633:; 1607:; 1581:; 1554:35 1552:. 1535:12 1497:49 1474:49 1442:. 1430:. 1426:. 1409:^ 1392:. 1368:69 1366:. 1323:21 1321:. 1317:. 1290:^ 1274:45 1272:. 1260:^ 1177:^ 1149:^ 1134:^ 1117:^ 1101:. 1081:^ 1071:. 1051:^ 1013:. 985:^ 970:^ 932:. 928:. 897:. 885:^ 862:. 803:, 707:. 619:; 596:, 483:. 443:) 323:. 278:, 271:. 247:. 212:, 181:, 32:A 1651:. 1625:. 1599:. 1564:. 1516:8 1450:. 1438:: 1403:. 1378:. 1374:: 1335:. 1329:: 1284:. 1280:: 1242:. 1171:. 1111:. 1097:: 1021:. 964:. 909:. 905:: 899:9 577:. 556:3 541:2 520:2 406:O 404:2 400:2 396:4 394:H 392:6 388:2 384:4 382:H 380:6 376:2 336:p 90:p 60:( 20:)

Index

Lichen spot tests
lichenology
spot analysis
lichens
reagent
dichotomous keys
lichen products
secondary metabolites
taxa
William Nylander
KOH
bleaching powder
calcium hypochlorite
p-phenylenediamine
filter paper
microscope
ultraviolet
fluoresce

foliose
Punctelia borreri
gyrophoric acid
reagent
aqueous solution
potassium hydroxide
sodium hydroxide
functional group
quinone
pigments
anthraquinones

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