Share to: share facebook share twitter share wa share telegram print page

Agnostida

Agnostida
Temporal range: Cambrian Stage 3 –Late Ordovician
Itagnostus interstrictus
Scientific classification Edit this classification
Domain: Eukaryota
Kingdom: Animalia
Phylum: Arthropoda
(unranked): Artiopoda
Subphylum: Trilobitomorpha
Class: Trilobita (?)
Order: Agnostida
Salter, 1864
Families

Suborder Agnostina

Suborder Eodiscina

Synonyms

Isopygia Gürich, 1907
Miomera Jækel, 1909

Agnostida are an order of extinct arthropods which have classically been seen as a group of highly modified trilobites, though some recent research has doubted this placement. Regardless, they appear to be close relatives as part of the Artiopoda.[1] They are present in the Lower Cambrian fossil record along with trilobites from the Redlichiida, Corynexochida, and Ptychopariida orders, and were highly diverse throughout the Cambrian. Agnostidan diversity severely declined during the Cambrian-Ordovician transition, and the last agnostidans went extinct in the Late Ordovician.[2]

Systematics

The Agnostida are divided into two suborders — Agnostina and Eodiscina — which are then subdivided into a number of families. As a group, agnostids are isopygous, meaning their pygidium is similar in size and shape to their cephalon. Most agnostid species were eyeless.

The systematic position of the order Agnostida within the class Trilobita remains uncertain, and there has been continuing debate whether they are trilobites or a stem group. The challenge to the status has focused on Agnostina partly due to the juveniles of one genus have been found with legs differing dramatically from those of adult trilobites,[3] suggesting they are not members of the lamellipedian clade, of which trilobites are a part. Instead, the limbs of agnostids closely resemble those of stem group crustaceans, although they lack the proximal endite, which defines that group. The study suggested that they were likely the sister taxon to the crustacean stem lineage, and, as such, part of the clade, Crustaceomorpha.[4] Other researchers have suggested, based on a cladistic analyses of dorsal exoskeletal features, that Eodiscina and Agnostida are closely united, and the Eodiscina descended from the trilobite order Ptychopariida.[5] A 2019 study of adult specimens with preserved soft tissue from the Burgess Shale found that agnostidans shared morphological similarities to trilobites and other related artiopodans like nektaspids, and their placement as stem-crustaceans was unsupported. The study recovered agnostidans as the sister group to other trilobites within the Artiopoda.[1]

Ecology

Scientists have long debated whether the agnostids lived a pelagic or a benthic lifestyle. Their lack of eyes, a morphology not well-suited for swimming, and their fossils found in association with other benthic trilobites suggest a benthic (bottom-dwelling) mode of life. They are likely to have lived on areas of the ocean floor which received little or no light and fed on detritus which descended from upper layers of the sea to the bottom. Their wide geographic dispersion in the fossil record is uncharacteristic of benthic animals, suggesting a pelagic existence. The thoracic segment appears to form a hinge between the head and pygidium allowing for a bivalved ostracodan-type lifestyle. The orientation of the thoracic appendages appears ill-suited for benthic living. Recent work suggests that some agnostids were benthic predators, engaging in cannibalism and possibly pack-hunting behavior.[6]

They are sometimes preserved within the voids of other organisms, for instance within empty hyolith conchs,[7] within sponges, worm tubes and under the carapaces of bivalved arthropods,[8] presumably in order to hide from predators or strong storm currents; or maybe whilst scavenging for food.[8] In the case of the tapering worm tubes Selkirkia, trilobites are always found with their heads directed towards the opening of the tube, suggesting that they reversed in; the absence of any moulted carapaces suggests that moulting was not their primary reason for seeking shelter.[8]

References

  1. ^ a b Moysiuk J, Caron JB (January 2019). "Burgess Shale fossils shed light on the agnostid problem". Proceedings. Biological Sciences. 286 (1894): 20182314. doi:10.1098/rspb.2018.2314. PMC 6367181. PMID 30963877.
  2. ^ Barnes BD, Sclafani JA, Zaffos A (April 2021). "Dead clades walking are a pervasive macroevolutionary pattern". Proceedings of the National Academy of Sciences of the United States of America. 118 (15). doi:10.1073/pnas.2019208118. PMC 8053996. PMID 33827921. S2CID 233184869.
  3. ^ Müller KJ, Walossek D (1987). "Morphology, ontogeny, and life habit of Agnostus pisiformis from the Upper Cambrian of Sweden". Fossils and Strata. 19: 1–124. doi:10.18261/8200075117-1987-01. ISBN 8200075117.
  4. ^ Bergström J, Hou XG (2005). "Early Palaeozoic non-lamellipedian arthropods". In Koenemann S, Ronald AJ (eds.). Crustacea and Arthropod Relationships. Taylor and Francis Group. pp. 75–93. ISBN 978-1-4200-3754-8.
  5. ^ Cotton TJ, Fortey RA (2005). "Comparative morphology and relationships of the Agnostida". In Koenemann S, Jenner RA (eds.). Crustacea and Arthropod Relationships. Vol. 16. Taylor and Francis Group. pp. 95–136. ISBN 978-1-4200-3754-8.
  6. ^ McMenamin MA (October 2010). "Cambrian cannibals: agnostid trilobite ethology and the earliest known case of arthropod cannibalism". Geological Society of America Abstracts with Programs. 42 (5): 320.
  7. ^ Fatka O, Vokáč V, Moravec J, Šinágl M, Valent M (January 2009). "Agnostids entombed in hyolith conchs". Memoirs of the Association of Australasian Palaeontologists. 37: 481–489.
  8. ^ a b c Chatterton BD, Collins DH, Ludvigsen R (2003). "Cryptic behaviour in trilobites: Cambrian and Silurian examples from Canada, and other related occurrences". In Lane PD, Siveter DJ, Fortey RA (eds.). Trilobites and Their Relatives. Special Papers in Palaeontology. Vol. 70. The Palaeontological Association. pp. 157–173. ISBN 978-0-901702-81-4.
Index: pl ar de en es fr it arz nl ja pt ceb sv uk vi war zh ru af ast az bg zh-min-nan bn be ca cs cy da et el eo eu fa gl ko hi hr id he ka la lv lt hu mk ms min no nn ce uz kk ro simple sk sl sr sh fi ta tt th tg azb tr ur zh-yue hy my ace als am an hyw ban bjn map-bms ba be-tarask bcl bpy bar bs br cv nv eml hif fo fy ga gd gu hak ha hsb io ig ilo ia ie os is jv kn ht ku ckb ky mrj lb lij li lmo mai mg ml zh-classical mr xmf mzn cdo mn nap new ne frr oc mhr or as pa pnb ps pms nds crh qu sa sah sco sq scn si sd szl su sw tl shn te bug vec vo wa wuu yi yo diq bat-smg zu lad kbd ang smn ab roa-rup frp arc gn av ay bh bi bo bxr cbk-zam co za dag ary se pdc dv dsb myv ext fur gv gag inh ki glk gan guw xal haw rw kbp pam csb kw km kv koi kg gom ks gcr lo lbe ltg lez nia ln jbo lg mt mi tw mwl mdf mnw nqo fj nah na nds-nl nrm nov om pi pag pap pfl pcd krc kaa ksh rm rue sm sat sc trv stq nso sn cu so srn kab roa-tara tet tpi to chr tum tk tyv udm ug vep fiu-vro vls wo xh zea ty ak bm ch ny ee ff got iu ik kl mad cr pih ami pwn pnt dz rmy rn sg st tn ss ti din chy ts kcg ve 
Prefix: a b c d e f g h i j k l m n o p q r s t u v w x y z 0 1 2 3 4 5 6 7 8 9 
Kembali kehalaman sebelumnya