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Lepidodendron

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environments. They sometimes reached heights of 50 metres (160 feet), and the trunks were often over 1 m (3 ft 3 in) in diameter. They are often known as "scale trees", due to their bark having been covered in diamond shaped leaf-bases, from which leaves grew during earlier stages of
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species were comparable in size to modern trees. The plants had tapering trunks as wide as 2 m (6.6 ft) at their base that rose to about 40 m (130 ft) and even 50 m (160 ft), arising from an underground system of horizontally spreading branches that were covered with
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is used when the leaf cushions and the majority of cortical tissues has decayed, with a shallow "fluted" surface remaining. However, it has been suggested that these are more likely growth forms than preserved bark types, as entire fossilized trunks have been discovered with dissimilar forms; if
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leaves formed a cylindrical shell around branches. The leaves were only present on thin and young branches, indicating that, though the lycopsid were evergreen, they did not retain their needles for as long as modern conifers. The leaf-cushions were fusiform and elongated, growing at most to a
799:. The rate of growth of arborescent lycophytes is disputed, some authors contended that they had a rapid life cycle, growing to their maximum size and dying in only 10 to 15 years, while other authors argue that these growth rates were overestimated. Rather than reproduce with seeds, 632:. Below the leaf scar the leaf-cushion tapered to a basal position. In this tapering area, circular impressions with fine pits were present. These impressions were continuous with the parichnos scars near the top of the tapering portion. This is because the impressions are formed by 1013: 654:
lycopsid grew the leaf-cushion only grew to a certain extent, past which the leaf-cushion stretched. This stretching widened the groove that separated the leaf-cushions, creating a broad, flat channel.
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layer cut a leaf from its base. Each leaf scar was composed of a central circular or triangular scar and two lateral scars that were smaller and oval-shaped. This central scar marks where the main
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grew as single, unbranched trunk, with leaves growing out of the scale leaf bases (cushions). Towards the end of the lycopod growth, the leaves on the lower part of the trunk were shed, and in
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lycopsid produced only secondary xylem. As the lycopods aged, the wood produced by the unifacial cambium decreased towards the top of the plant such that terminal twigs resembled young
646:. In some leaf-cushions a second depression was present above the ligular pit. Though its purpose is unclear, it has been suggested that the depression may mark the position of a 1889: 1884: 1630:"End Permian to Middle Triassic plant species richness and abundance patterns in South China: Coevolution of plants and the environment through the Permian–Triassic transition" 959: 871:(in its broad sense) only becoming extinct around the end of the Permian, around 252 million years ago, as a result of the extreme environmental disturbance caused by the 1446: 1278: 1800: 975: 711: 636:
tissue that developed in closely with the parichnos. Above the leaf scar was a deep triangular impression known as the "ligular pit" for its similarities to the
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situated on fertile stems that grew on or near the main trunk. The fertile stems grew together in cone-like structures that clustered at the tips of branches.
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stems. Compared to modern trees, the stems and branches of the lycopsids contained little wood with the majority of mature stems consisting of a massive
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decay is assumed to be constant throughout the trunk, then different forms indicate growth rather than levels of decay. It is likely that the trunk of
687:. These rhizomorphic axes were shoot-like, and dichotomous branching of the rootlets structured the stigmarian systems. Rootlet scars can be seen from 1879: 1874: 1774: 1718:
J. M. Anderson and H. M. Anderson. 1985. Palaeoflora of Southern Africa. Prodromus of South African Megafloras Devonian to Lower Cretaceous 1-423
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Xu, Zhen; Hilton, Jason; Yu, Jianxin; Wignall, Paul B.; Yin, Hongfu; Xue, Qing; Ran, Weiju; Li, Hui; Shen, Jun; Meng, Fansong (September 2022).
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depended on their outer bark rather than their vascular tissues, as compared to modern trees that rely mostly on their central mass of wood.
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regions. The lycopsid inhabited an extensive area compared to tropical flora of the same time period, with lycopods growing as far north as
517:. The nearly-uniform growth of this cortical tissue indicates no difference in growth during changing seasons, and the absence of dormant 859:
became extinct at the end of the Carboniferous, as part of a broader pattern of ecological change, including the increasing dominance of
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of the stem into the leaf. This forked strand is sometimes referred to as the "parichnos". Surrounding this strand were
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The leaves of the lycopsid were needle-like and were densely spiraled about young shoots, each possessing only a single
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and dormant buds indicates no seasonal growth patterns, and modern plants with similar characteristics tend to grow in
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cells and occasionally thick-walled elements. Surrounding both conducting tissues was a broad sheath of transfusion
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Strullu-Derrien, Christine; Strullu, Désiré-Georges (November 2007). "Mycorrhization of fossil and living plants".
1974: 1944: 1023: 1534:"A new Bergeria (Flemingitaceae) from the Mississippian of Xinjiang, NW China and its evolutionary implications" 546:
formed peg-like projections that stretched and tore as the bark stretched. To resist the bending force of wind,
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in lowland wetland forests, and increasingly arid-adapted vegetation across western Pangea. However, in the
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of the leaf connected to the vascular system of the stem. This xylem bundle was composed only of primary
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many rootlets. Though the height of the lycopsids make the plants similar to modern trees, the constant
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Thomas, B.A. and Watson, Joan (1976). "A rediscovered 114-foot Lepidodendron from Bolton, Lancashire".
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region comprising what is now China, wet tropical environmental conditions continued to prevail, with
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growth. However, they are correctly defined as arborescent lycophytes. They thrived during the
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Lucas, Spencer G.; DiMichele, William A.; Opluštil, Stanislav; Wang, Xiangdong (2023-06-14).
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cambium of modern trees. Though the bifacial cambium of modern trees produces both secondary
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that contrasts with that of modern trees. At the ends of branches were oval-shaped
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Geografiia rastenii s osnovani botaniki (Geography of plants and basics of botany)
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is both used for the whole plant as well as specifically the stems and leaves.
1558: 1533: 1155: 1134: 860: 852: 700: 669: 647: 633: 625: 609: 585: 92: 57: 1750: 1614: 1567: 1206:Палеонтологический музей имени Ю.А. Орлова (The Orlov Museum of Paleontology) 1343: 1148: 864: 804: 675: 605: 590: 570: 543: 444: 420: 170: 97: 1606: 1490: 1362: 529:
species. The outermost cortex of oldest stems developed into the bark-like
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and similar lycopsid species known from the fossil record including
1508:(illustrated ed.). University of Michigan Press. p. 429. 1296:(illustrated ed.). University of Chicago Press. p. 321. 770: 730:
genera have been described to name the various levels of decay in
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around 252 million years ago. Sometimes erroneously called "giant
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Extinct genus of vascular plants of the Carboniferous to Triassic
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Feng, Ru; D’Rozario, Ashalata; Zhang, Jian-Wei (December 2019).
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Vulf, Evgenii Vladimirovich and Brissenden, Elizabeth (1943).
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lycopsids reproduced with spores. The spores were stored in
1247:. Vol. 1. Cambridge University Press. pp. 93–192. 742:
is used when cushions have been removed by deep decay, and
536:. The bark of the lycopsid was somewhat similar to that of 604: in). The middle of leaf-cushions were smooth, where 594:
length of 8 cm (3 in) and a width of 2 cm (
342:", the genus was actually more closely related to modern 1084:, showing dichotomous branching at the top of the trunk 1022:
stem impression displayed at a collection held in the
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Hetherington, A.J.; Berry, C.M.; Dolan, Liam (2016).
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Thomas, Barry A.; Cleal, Christopher J. (May 2018).
679:. The rootlets were dichotomously branched from the 1734: 378: 738:describes stems that have lost their epidermises, 691:fossils where the root hairs used to be attached. 1244:Fossil plants: for students of botany and geology 1587:Geological Society, London, Special Publications 1267:. Chronica Botanica Company. pp. 176–177. 451:that had a similar shape to modern cones of a 1264:An introduction to historical plant geography 8: 1445:: CS1 maint: multiple names: authors list ( 1277:: CS1 maint: multiple names: authors list ( 583:species are indistinguishable from those of 1890:Paleozoic life of the Northwest Territories 1885:Paleozoic life of Newfoundland and Labrador 1256: 1254: 1185:. Gos. nauchno-pedagog. izd-vo. p. 167 751:lycopsids were subject to the growth forms 695:are occasionally present in the tissues of 579:in others, though in general the leaves of 1722: 1504:John Adam Dorr, Donald F. Eschman (1970). 1236: 1234: 1232: 779:, showing the unbranched trunk with leaves 321:grew as large-tree-like plants in wetland 113: 31: 1557: 1480: 1352: 1342: 1174: 1172: 763:progressing up the trunk, respectively. 710: 411: 122:Trunk fragment, showing leaf base scars 1168: 1041:diagrams from the Geological Survey of 882: 1438: 1270: 699:lycopsids, indicating the presence of 334:), and persisted until the end of the 1675:. Washington, DC: Smithsonian Books. 1527: 1525: 1458: 1456: 7: 827:species were distributed throughout 313:vascular plants belonging the order 1870:Carboniferous life of North America 1671:Davis, Paul; Kenrick, Paul (2004). 783:During the early stages of growth, 346:than to modern club mosses. In the 1419:(1). Wiley Online Library: 15–20. 1294:The Evolutionary Biology of Plants 720:Estonian Museum of Natural History 25: 873:Permian-Triassic extinction event 1080:1911 reconstruction of a mature 1073: 1049: 1030: 1012: 993: 974: 958: 946: 932: 918: 904: 885: 673:are assigned to the form taxon, 483:The stem of the lycopsids had a 131: 43:Early Carboniferous–Late Permian 1880:Paleozoic life of New Brunswick 1875:Fossils of Georgia (U.S. state) 1654:10.1016/j.earscirev.2022.104136 1241:Seward, Albert Charles (1898). 1209:. Moscow: PIN RAN. p. 56. 1110:Evolutionary history of plants 791:, the upper part of the trunk 663:The underground structures of 521:further indicates the lack of 490:cambium, contrasting with the 1: 1980:Fossil taxa described in 1820 1895:Paleozoic life of Nova Scotia 775:Reconstruction of a juvenile 1985:Prehistoric lycophyte genera 269:Anderson & Anderson 1986 940:Lepidodendron lycopodioides 502:, the unifacial cambium of 379: 2001: 1694:. Portland: Timber Press. 1692:A Natural History of Ferns 1538:Journal of Palaeogeography 1398:10.1016/j.crpv.2007.09.006 289:B.A.Thomas & C.J.Cleal 1925:Permian life of Australia 1920:Paleozoic life of Oceania 1900:Paleozoic life of Nunavut 1690:Morran, Robin C. (2004). 1559:10.1186/s42501-018-0020-4 1024:National Museum of Brazil 283: 276: 238: 231: 128:Scientific classification 126: 121: 112: 34: 1970:Paleozoic life of Europe 1905:Paleozoic life of Quebec 18:Lepidodendron dichotomum 1915:Fossils of South Africa 1344:10.1073/pnas.1514427113 1292:Karl J. Niklas (1997). 926:Lepidodendron aculeatum 767:Growth and reproduction 734:bark fossils. The name 395:Description and biology 330:Period (358.9 to 298.9 1965:Fossils of South Korea 1955:Fossils of North Korea 1935:Paleozoic life of Asia 1855:Prehistoric lycophytes 1607:10.1144/SP535-2022-334 1378:Comptes Rendus Palevol 1203:A. V. Lopatin (2012). 1179:V. V. Alekhin (1961). 780: 723: 659:Underground Structures 566: 480: 471:Leaf scars shown on a 439:of branches created a 428: 409: 1827:Paleobiology Database 1634:Earth-Science Reviews 1433:10.1002/gj.3350110102 988:, Nova Scotia, Canada 912:Lepidodendron elegans 899:, Lower Pennsylvanian 823:conditions. However, 774: 714: 650:. As the branch of a 608:were created when an 561: 470: 415: 407: 1950:Fossils of Indonesia 1930:Fossils of Australia 1865:Pennsylvanian plants 835:and as far south as 1646:2022ESRv..23204136X 1599:2023GSLSP.535..334L 1550:2019JPalG...8....4F 1506:Geology of Michigan 1425:1976GeolJ..11...15T 1390:2007CRPal...6..483S 1335:2016PNAS..113.6695H 1062:Upper Carboniferous 1007:, Glasgow, Scotland 1003:fossil stumps from 969:with leafy branches 348:form classification 1413:Geological Journal 781: 724: 567: 481: 429: 410: 1860:Prehistoric trees 1842: 1841: 1814:Open Tree of Life 1728:Taxon identifiers 1482:10.1111/nph.14903 1329:(24): 6695–6700. 1216:978-5-903825-14-1 1056:External mold of 1020:Lepidodendron sp. 893:Lepidodendron sp. 716:Lepidodendron sp. 492:bifacial vascular 332:million years ago 295: 294: 287:Dimicheleodendron 266:L. whitehillianum 227: 16:(Redirected from 1992: 1975:Fossils of Italy 1945:Fossils of China 1835: 1834: 1822: 1821: 1809: 1808: 1796: 1795: 1783: 1782: 1770: 1769: 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The 588: 587: 582: 581:Lepidodendron 578: 577: 572: 565: 564:Lepidodendron 560: 553: 551: 549: 548:Lepidodendron 545: 541: 540: 535: 532: 531:lycopodiopsid 528: 527:Lepidodendron 524: 520: 516: 513: 509: 508:Lepidodendron 505: 504:Lepidodendron 501: 497: 493: 489: 486: 478: 477:Lepidodendron 474: 473:Lepidodendron 469: 462: 460: 458: 454: 450: 449:Lepidostrobus 446: 442: 438: 433: 432:Lepidodendron 426: 425:Lepidodendron 422: 418: 417:Lepidostrobus 414: 406: 399: 394: 392: 390: 387: 384:, scale, and 383: 381: 376: 373: 369: 368:Lepidodendron 361: 359: 357: 356:Lepidodendron 353: 349: 345: 341: 337: 333: 329: 328:Carboniferous 324: 320: 319:Lepidodendron 316: 312: 309:of primitive 308: 305: 301: 300: 299:Lepidodendron 288: 285: 284: 282: 279: 275: 267: 264: 259: 256: 253:Chachlov 1948 251: 248: 243: 240: 239: 237: 234: 230: 223: 222: 221:Lepidodendron 215: 212: 211: 208: 202: 199: 198: 195: 189: 186: 185: 182: 179: 176: 175: 172: 169: 166: 163: 162: 159: 158:Tracheophytes 156: 153: 150: 149: 146: 143: 140: 139: 134: 129: 125: 120: 116: 111: 104: 99: 94: 89: 84: 79: 74: 69: 64: 59: 54: 49: 37: 36:Lepidodendron 33: 30: 19: 1735: 1691: 1672: 1637: 1633: 1623: 1590: 1586: 1576: 1541: 1537: 1505: 1499: 1472: 1468: 1441:cite journal 1416: 1412: 1406: 1381: 1377: 1371: 1326: 1322: 1312: 1293: 1287: 1263: 1243: 1220:. 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Retrieved 1181: 1154: 1147: 1140: 1133: 1126: 1121:Glossopteris 1119: 1115:Fossil Grove 1102: 1095: 1081: 1057: 1043:Pennsylvania 1038: 1019: 1005:Fossil Grove 1000: 981: 966: 939: 925: 911: 892: 868: 856: 850: 824: 817:growth rings 815:The lack of 814: 811:Distribution 800: 788: 784: 782: 776: 760: 756: 752: 748: 743: 739: 735: 731: 725: 715: 696: 688: 684: 674: 668: 664: 662: 651: 641: 584: 580: 574: 568: 563: 547: 542:species, as 537: 526: 507: 503: 482: 476: 472: 448: 431: 430: 424: 416: 388: 377: 367: 365: 355: 318: 298: 297: 296: 286: 265: 257: 249: 242:L. aculeatum 241: 220: 219: 164: 151: 35: 29: 1788:iNaturalist 1760:Wikispecies 1593:(1): 1–15. 861:seed plants 841:latitudinal 833:Spitsbergen 829:subtropical 701:mycorrhizal 683:similar to 523:seasonality 479:lycophytes. 408:Restoration 352:paleobotany 340:club mosses 323:coal forest 258:L. obovatum 1849:Categories 1640:: 104136. 1222:2020-10-05 1189:2020-10-05 1163:References 1156:Sigillaria 1135:Lycophytes 984:bark from 853:Euramerica 847:Extinction 757:Aspidiaria 740:Aspidiariu 726:Different 670:Sigillaria 648:sporangium 634:aerenchyma 626:parenchyma 610:abscission 606:leaf scars 586:Sigillaria 544:leaf scars 427:lycophytes 344:quillworts 311:lycopodian 250:L. batovii 171:Lycophytes 1615:0305-8719 1568:2524-4507 1273:cite book 1149:Stigmaria 1060:from the 865:Cathaysia 805:sporangia 689:Stigmaria 676:Stigmaria 630:tracheids 591:decurrent 485:unifacial 437:dichotomy 421:strobilus 366:The name 362:Etymology 141:Kingdom: 1745:Wikidata 1544:(1): 4. 1491:29282734 1363:27226309 1142:Lycopsid 1090:See also 1037:Various 821:tropical 761:Bergeria 736:Bergeria 681:rhizomes 562:Leaf of 534:periderm 515:meristem 512:cortical 488:vascular 445:strobili 400:Overview 391:, tree. 278:Synonyms 200:Family: 1819:5154628 1806:1071081 1780:4894389 1751:Q576530 1642:Bibcode 1595:Bibcode 1546:Bibcode 1421:Bibcode 1386:Bibcode 1354:4914198 1331:Bibcode 986:Joggins 879:Gallery 839:, in a 753:Knorria 744:Knorria 685:Isoetes 643:Isoetes 618:trachea 599:⁄ 447:called 389:dendron 386:δένδρον 336:Permian 304:extinct 233:Species 213:Genus: 187:Order: 177:Class: 145:Plantae 1832:125629 1793:202859 1712:  1698:  1679:  1613:  1566:  1512:  1489:  1361:  1351:  1300:  1213:  759:, and 728:fossil 693:Hyphae 638:ligule 622:cortex 554:Leaves 496:phloem 453:spruce 419:, the 302:is an 1801:IRMNG 797:crown 707:Decay 539:Picea 500:xylem 441:habit 380:lepis 375:λεπίς 372:Greek 307:genus 165:Clade 152:Clade 1775:GBIF 1710:ISBN 1696:ISBN 1677:ISBN 1611:ISSN 1564:ISSN 1510:ISBN 1487:PMID 1447:link 1359:PMID 1323:PNAS 1298:ISBN 1279:link 1211:ISBN 1066:Ohio 571:vein 519:buds 498:and 463:Stem 48:PreꞒ 1650:doi 1638:232 1603:doi 1591:535 1554:doi 1477:doi 1473:218 1429:doi 1394:doi 1349:PMC 1339:doi 1327:113 1064:of 851:In 640:of 525:in 457:fir 455:or 423:of 1851:: 1829:: 1816:: 1803:: 1790:: 1777:: 1762:: 1747:: 1648:. 1636:. 1632:. 1609:. 1601:. 1589:. 1585:. 1562:. 1552:. 1540:. 1536:. 1524:^ 1485:. 1471:. 1467:. 1455:^ 1443:}} 1439:{{ 1427:. 1417:11 1415:. 1392:. 1380:. 1357:. 1347:. 1337:. 1325:. 1321:. 1275:}} 1271:{{ 1253:^ 1231:^ 1171:^ 875:. 855:, 755:, 459:. 354:, 167:: 154:: 98:Pg 1704:. 1685:. 1656:. 1652:: 1644:: 1617:. 1605:: 1597:: 1570:. 1556:: 1548:: 1542:8 1518:. 1493:. 1479:: 1449:) 1435:. 1431:: 1423:: 1400:. 1396:: 1388:: 1382:6 1365:. 1341:: 1333:: 1306:. 1281:) 1225:. 1192:. 1068:. 722:. 601:4 597:3 217:† 204:† 191:† 103:N 93:K 88:J 83:T 78:P 73:C 68:D 63:S 58:O 53:Ꞓ 20:)

Index

Lepidodendron dichotomum
PreꞒ

O
S
D
C
P
T
J
K
Pg
N

Scientific classification
Edit this classification
Plantae
Tracheophytes
Lycophytes
Lycopodiopsida
Lepidodendrales
Lepidodendraceae
Lepidodendron
Species
Synonyms
extinct
genus
lycopodian
Lepidodendrales
coal forest

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