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Pelvic spur

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72:. Nonetheless, uses for the structures have been thoroughly documented. Species that have external spurs have corresponding muscles, neurological structures, and vascularization to allow for independent movement. The spurs are more pronounced and visible in male specimens and have been observed in use during courtship behavior. The spurs are specifically used in the clasping and stimulation of females by males during courtship and mating. In certain species, males will also use their spurs to engage in combat with one another. 34: 846: 789: 20: 367:), with anterior to posterior spur movements varying in speed of undulation by phase. Furthermore, the males exhibited use of the spurs to better position or adjust the female’s cloaca for mating. The authors note that spur use for combat can also be observed in this species between males. A separate study found similar results in diamond pythons ( 340:), an arboreal species. In this species, researchers did not observe biting. In fact, the authors observed that the heads of combating males were frequently out of sight of one another. In its place, observed males would tightly grip on to each other using the posterior regions of their bodies, orienting their spurs to be 373:), a species that does not exhibit any bouts of combat between males. In this species, multiple males were observed mating with the same female simultaneously, and males did not engage in combat. Instead, it was observed that spurs were used by males to manipulate the tail of the female. Corroborating these results in a 112:
exhibited a sacrum, pelvic girdle, and robust hind limb structures outside of the ribcage, all of which led researchers to the conclusion that these hind limbs were functional for locomotion. The significance of this finding is great, as there were three other known species of legged snakes from this
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Similar to the described observations of sexual dimorphism prior to their publication, William H. Stickel and Luccille F. Stickel also noted that observations had been made by others of pelvic spur use by males on females during mating. These observations have since been formally investigated and
315:). The authors of this study noted that others in the field had made similar observations before, but had not formally researched the topic specifically. Spurs were found to be significantly larger in males, while in females spurs were much shorter, and were sometimes externally absent. 383:. It was observed that males repeatedly alternated the orientation of the spurs between horizontal and vertical positions, which the authors suggest stimulated muscle contractions in the female, which would allow for better alignment between the individuals for mating. 62:. These spurs are made up of the remnants of the femur bone, which is then covered by a corneal spur, or claw-like structure. This femur derives from ancestral hind limbs found in the most recent common ancestor of modern snakes and the other reptiles of the clade 424:
Palci, A., Hutchinson, M. N., Caldwell, M. W., Smith, K. T., & Lee, M. S. Y. (2019). The homologies and evolutionary reduction of the pelvis and hindlimbs in snakes, with the first report of ossified pelvic vestiges in an anomalepidid (Liotyphlops beui).
68:, many of which have fully functional front and hind limbs. Due to the fact that the spurs derive from the ancestral state of functional legs, but are no longer functional for locomotion specifically, these structures meet the criteria for being considered 344:
to their body while doing so. The authors postulate that this form of spur-based combat is adaptive to the species’ arboreal habitat. It is also worth noting that combat between males in species that lack spurs, such as species of
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While these are the most well-known taxa to possess spurs, evidence does exist for the presence of ossified vestigial structures in other taxa. A 2019 publication provided evidence for similarly ossified structures in the species
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Garberoglio, F. F., Apesteguía, S., Simões, T. R., Palci, A., Gómez, R. O., Nydam, R. L., Larsson, H. C. E., Lee, M. S. Y., & Caldwell, M. W. (2019). New skulls and skeletons of the Cretaceous legged snake
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Recent analysis of numerous fossil records supported these findings and further demonstrated the reduction of pelvic and hind limb structures within these lineages. Further evidence for these structures being
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Research has since found the use of pelvic spurs in dominance displays in numerous species. The use of spurs alongside biting was observed in displays between males in a captive group of Indian pythons
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are poorly understood due to their cryptic nature and are typically small in size, fossorial, and worm-like. This 2019 study is the first described occurrence of these structures within the family
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Lee, M. S. Y., Hugall, A. F., Lawson, R., & Scanlon, J. D. (2007). Phylogeny of snakes (Serpentes): Combining morphological and molecular data in likelihood, Bayesian and parsimony analyses.
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Barker, D. G., Murphy, J. B., & Smith, K. W. (1979). Social behavior in a captive group of indian pythons, python molurus (Serpentes, boidae) with formation of a linear social hierarchy.
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Anzai, R. K., Eleuterio, N. F., Oliveira Lima, T. D., Manfio, R. H., & Almeida Santos, S. M. D. (2023). Pelvic spur use during courtship and mating in the red-tailed boa Boa constrictor.
334:. The position in this hierarchy was directly correlated with a male’s number of successful instances of mating. Another study found the use of spurs in madagascan boas ( 80:
The fossil record of snakes is not expansive. Nonetheless, multiple fossilized specimens document the progression of the development of leglessness within the suborder
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Carpenter, C. C., Murphy, J. B., & Mitchell, L. A. (1978). Combat bouts with spur use in the madagascan boa(Sanzinia madagascariensis).
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Slip, D. J., & Shine, R. (1988). The reproductive biology and mating system of diamond pythons, morelia spilota(Serpentes: Boidae).
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Gillingham, J. C., & Chambers, J. A. (1982). Courtship and pelvic spur use in the burmese python, python molurus bivittatus.
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is well documented - in these superfamilies, spurs can be observed as tools for courtship and competition between males, and are
241:. These basal clades are sometimes referred to as primitive snakes, as they are considered to be the earliest diverging taxa of 880: 830: 587: 361:
One such study found dynamic use of spurs by males during different phases of courtship and mating in Burmese pythons (
916: 873: 158: 147:, and the three extinct species previously described were more closely related to modern-day snakes belonging to 245:, the clade which includes the majority of described living snake species. The presence and use of spurs across 305:
nature of the spurs was formally described by William H. Stickel and Luccille F. Stickel in 1946 in the genus
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ApesteguĂ­a, S., & Zaher, H. (2006). A Cretaceous terrestrial snake with robust hindlimbs and a sacrum.
131:, but all were predicted to have been marine species, and all of them lacked the sacrum region found in 262: 704:
Gillingham, J. C. (1980). Communication and combat behavior of the black rat snake(Elaphe obsoleta).
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was first described in 2006, and has been proposed as the earliest branching taxa of the suborder
368: 173:. These taxa possess a triradiate pelvis, which can also be observed in the skeletons of modern 906: 627:
Stickel, W. H., & Stickel, L. F. (1946). Sexual dimorphism in the pelvic spurs of enygrus.
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Numerous studies have been conducted on the use of pelvic spurs by males in the superfamilies
911: 349:, relies on a distinct repertoire of behaviors that differs from species possessing spurs. 8: 816: 331: 767: 713: 689: 569: 861: 804: 588:
https://www.ucl.ac.uk/museums-static/obl4he/vertebratediversity/serpentes_snakes.html
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species, a study in 2023 documented the use of spurs in mating by red-tailed boas,
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do not possess spurs, nor do members of the most populous group within
126: 120: 64: 845: 374: 97: 744: 664: 640: 137:. The paleontologists thus concluded via phylogenetic analysis that 556:
Bellairs, A. D., & Underwood, G. (1951). The origin of snakes.
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of can be found in the pelvis of some living taxa such as
207:. However, spurs are present among the basal clades of 501:, and the evolution of the modern snake body plan. 185:The presence of pelvic spurs in extant species of 898: 288: 881: 824: 586:. (n.d.). Retrieved October 10, 2023, from 888: 874: 831: 817: 427:Zoological Journal of the Linnean Society 281:, which is one of three families within 32: 18: 41:showing the bones inside the anal spurs 23:External view of anal spurs on a male, 899: 352: 330:), which subsequently formed a linear 754: 752: 727: 725: 676: 674: 672: 623: 621: 619: 318: 840: 783: 579: 577: 528: 526: 524: 522: 492: 490: 452: 450: 448: 446: 444: 442: 420: 418: 416: 414: 412: 398: 396: 56:belonging to the greater infraorder 13: 749: 722: 669: 616: 570:10.1111/j.1469-185X.1951.tb00646.x 271:. Members of this sister group of 14: 928: 574: 519: 487: 439: 409: 393: 844: 787: 143:is the most ancient taxa within 96:. The fossils were found in the 75: 698: 645: 358:published in multiple species. 180: 86:. The species of extinct snake 592: 550: 474: 309:(more commonly known today as 1: 386: 289:Importance to social behavior 16:Modified reptilian appendages 860:. You can help Knowledge by 803:. You can help Knowledge by 600:Systematics and Biodiversity 402:Pough, F. H. (Ed.). (2004). 189:is limited. Most members of 52:in certain superfamilies of 7: 480:Bauchot, R. (Ed.). (1994). 458:The Herpetological Bulletin 10: 933: 839: 782: 229:, and among one member of 116:Pachyrhachis problematicus 612:10.1017/S1477200007002290 482:Snakes: A natural history 435:10.1093/zoolinnean/zlz098 364:Python molurus bivittatus 337:Sanzinia madagascariensis 917:Vertebrate anatomy stubs 406:(3rd ed). Prentice Hall. 104:, and were dated to the 122:Haasiophis terrasanctus 106:Upper Cretaceous period 856:–related article is a 515:10.1126/sciadv.aax5833 42: 30: 128:Eupodophis descouensi 36: 22: 546:10.1038/nature04413 540:(7087), 1037–1040. 470:10.33256/hb163.3536 353:Courtship behaviors 332:dominance hierarchy 854:vertebrate anatomy 558:Biological Reviews 319:Dominance displays 303:sexually dimorphic 267:of the infraorder 255:sexually dimorphic 43: 31: 869: 868: 812: 811: 584:Serpentes(Snakes) 110:Najash rionegrina 89:Najash rionegrina 924: 890: 883: 876: 848: 841: 833: 826: 819: 791: 784: 774: 756: 747: 729: 720: 702: 696: 678: 667: 649: 643: 625: 614: 596: 590: 581: 572: 554: 548: 530: 517: 509:(11), eaax5833. 503:Science Advances 494: 485: 478: 472: 454: 437: 422: 407: 400: 264:Liotyphlops beui 170:Eunectes murinus 164:Candoia carinata 932: 931: 927: 926: 925: 923: 922: 921: 897: 896: 895: 894: 838: 837: 780: 778: 777: 757: 750: 745:10.2307/1444292 730: 723: 703: 699: 679: 670: 665:10.2307/1443224 650: 646: 641:10.2307/1438812 626: 617: 597: 593: 582: 575: 555: 551: 531: 520: 495: 488: 484:. Sterling Pub. 479: 475: 455: 440: 423: 410: 401: 394: 389: 380:Boa constrictor 370:Morelia spilota 355: 321: 291: 238:Cylindrophiidae 211:, including in 183: 78: 17: 12: 11: 5: 930: 920: 919: 914: 909: 893: 892: 885: 878: 870: 867: 866: 849: 836: 835: 828: 821: 813: 810: 809: 792: 776: 775: 766:(4), 396–404. 748: 721: 712:(2), 120–127. 697: 688:(2), 207–212. 668: 644: 615: 606:(4), 371–389. 591: 573: 564:(2), 193–237. 549: 518: 486: 473: 438: 408: 391: 390: 388: 385: 354: 351: 327:Python molurus 320: 317: 290: 287: 278:Anomalepididae 243:Alethinophidia 209:Alethinophidia 198:Alethinophidia 182: 179: 150:Alethinophidia 77: 74: 59:Alethinophidia 39:Boelens python 37:Skeleton of a 28:burmese python 15: 9: 6: 4: 3: 2: 929: 918: 915: 913: 910: 908: 907:Snake anatomy 905: 904: 902: 891: 886: 884: 879: 877: 872: 871: 865: 863: 859: 855: 850: 847: 843: 842: 834: 829: 827: 822: 820: 815: 814: 808: 806: 802: 799:article is a 798: 793: 790: 786: 785: 781: 773: 769: 765: 761: 760:Herpetologica 755: 753: 746: 742: 738: 734: 728: 726: 719: 715: 711: 707: 706:Herpetologica 701: 695: 691: 687: 683: 682:Herpetologica 677: 675: 673: 666: 662: 658: 654: 648: 642: 638: 634: 630: 624: 622: 620: 613: 609: 605: 601: 595: 589: 585: 580: 578: 571: 567: 563: 559: 553: 547: 543: 539: 535: 529: 527: 525: 523: 516: 512: 508: 504: 500: 493: 491: 483: 477: 471: 467: 463: 459: 453: 451: 449: 447: 445: 443: 436: 432: 428: 421: 419: 417: 415: 413: 405: 399: 397: 392: 384: 382: 381: 376: 372: 371: 366: 365: 359: 350: 348: 343: 342:perpendicular 339: 338: 333: 329: 328: 316: 314: 313: 308: 304: 300: 296: 286: 284: 283:Scolecophidia 280: 279: 274: 273:Scolecophidia 270: 269:Scolecophidia 266: 265: 258: 256: 252: 248: 244: 240: 239: 234: 233: 228: 227: 222: 221: 216: 215: 210: 206: 205: 200: 199: 194: 193: 192:Scolecophidia 188: 178: 176: 172: 171: 166: 165: 160: 159:plesiomorphic 154: 152: 151: 146: 142: 141: 140:N. rionegrina 136: 135: 134:N. rionegrina 130: 129: 124: 123: 118: 117: 113:time period, 111: 107: 103: 99: 95: 91: 90: 85: 84: 76:Fossil record 73: 71: 67: 66: 61: 60: 55: 51: 47: 40: 35: 29: 26: 21: 862:expanding it 851: 805:expanding it 794: 779: 763: 759: 736: 732: 709: 705: 700: 685: 681: 656: 652: 647: 632: 628: 603: 599: 594: 583: 561: 557: 552: 537: 533: 506: 502: 498: 481: 476: 461: 457: 426: 403: 378: 369: 363: 360: 356: 346: 335: 326: 322: 310: 306: 298: 294: 292: 282: 276: 272: 268: 263: 259: 250: 246: 242: 236: 232:Uropeltoidea 230: 224: 218: 212: 208: 202: 196: 190: 186: 184: 181:Distribution 169: 162: 155: 148: 144: 139: 133: 127: 121: 115: 109: 93: 87: 82: 79: 63: 57: 46:Pelvic spurs 45: 44: 912:Snake stubs 404:Herpetology 347:Caenophidia 299:Pythonoidea 251:Pythonoidea 226:Amerophidia 220:Pythonoidea 204:Caenophidia 901:Categories 739:(1), 193. 659:(3), 466. 429:, zlz098. 387:References 100:region of 65:Toxicofera 635:(1), 10. 464:, 35–36. 375:New World 223:, among 187:Serpentes 145:Serpentes 102:Argentina 98:Patagonia 94:Serpentes 83:Serpentes 70:vestigial 772:3892404 718:3891474 694:3891678 312:Candoia 307:Enygrus 295:Booidea 247:Booidea 214:Booidea 175:lizards 770:  733:Copeia 716:  692:  653:Copeia 629:Copeia 534:Nature 499:Najash 301:. The 235:, the 201:, the 54:snakes 50:cloaca 25:albino 852:This 797:snake 795:This 768:JSTOR 714:JSTOR 690:JSTOR 858:stub 801:stub 737:1982 657:1979 633:1946 297:and 249:and 217:and 125:and 741:doi 661:doi 637:doi 608:doi 566:doi 542:doi 538:440 511:doi 466:doi 462:163 431:doi 167:or 903:: 764:44 762:, 751:^ 735:, 724:^ 710:36 708:, 686:34 684:, 671:^ 655:, 631:, 618:^ 602:, 576:^ 562:26 560:, 536:, 521:^ 505:, 489:^ 460:, 441:^ 411:^ 395:^ 285:. 257:. 177:. 153:. 119:, 108:. 889:e 882:t 875:v 864:. 832:e 825:t 818:v 807:. 743:: 663:: 639:: 610:: 604:5 568:: 544:: 513:: 507:5 468:: 433:: 324:(

Index


albino
burmese python

Boelens python
cloaca
snakes
Alethinophidia
Toxicofera
vestigial
Serpentes
Najash rionegrina
Patagonia
Argentina
Upper Cretaceous period
Pachyrhachis problematicus
Haasiophis terrasanctus
Eupodophis descouensi
N. rionegrina
N. rionegrina
Alethinophidia
plesiomorphic
Candoia carinata
Eunectes murinus
lizards
Scolecophidia
Alethinophidia
Caenophidia
Booidea
Pythonoidea

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