Kerygmachela kierkegaardi

克尔凯郭尔宣扬爪虫

100%

3D animation

2D animation

2D animation

2D animation

分类学

门: 节肢动物门

纲: 恐虾纲

目:未定

科:未定

属: 宣扬爪虫

种: 克尔凯郭尔宣扬爪虫

描述: 

       这种古老的生物体长在1到10英寸之间,身体两侧有11个褶皱皮瓣。多刺的的前附肢表明宣扬爪虫可能是掠食者;然而,化石表明,它的总尺寸约为175毫米,嘴巴相对较小,这表明它只适合捕食非常小的猎物。这种掠食者还拥有圆形的头和一个细长的尾刺。头部形成一个圆形的前叶,在前附肢之间延伸。宣扬爪虫头部有一对发育良好的前附肢,与其他恐虾目和西伯利亚虫目的相对应。每一根末端都有一串长刺。一对无柄、狭缝状复眼位于这些附肢的基部稍后方。根据前附肢的位置和保存情况,其基部认为是眼睛,具有独特的突起和高反射率,类似于布尔吉斯页岩种节肢动物眼睛的保存情况。它们的轮廓让人想起三叶虫的肾状或镰刀状的眼叶。眼睛位于腹外侧,因为在腹侧标本中,口部结构和吻侧刺清晰可见时眼睛的位置最具有参考性。在背侧标本中,表皮环纹持续覆盖在眼叶上。眼睛的前半部位于前附肢的后部。在克尔凯郭尔宣扬爪虫中看到的视觉结构代表了原始复眼。一个小的面向前方的嘴巴位于头部下方,并有一对匕首状结构。头部还具有一个中叶状的突起物,携带一对小的、可能的眼结构。躯干由11个体节组成,每节上有4个背侧瘤,与11对背侧鳃样结构的皮瓣,以及11对位于皮瓣下方的小肢(叶足)。身体末端只有一根不分节的尾刺,以前被认为是一对。宣扬爪虫在内部拥有一个发育良好的咽和一个有8对节肢动物型的消化腺的中肠。脑由前脑(最前部的大脑神经节)组成,神经分支延伸至正中叶、额附肢和眼睛。轴部有11排瘤点,对应于每组皮瓣侧边生长,每排有4个瘤点。后面瘤点变得更为突出。中间两个瘤点比外侧的大,越往后面中间俩瘤点之间的距离越大,最终在远端几乎与外侧俩瘤点重叠。侧皮瓣依次向后缩小。在新材料中,第4和第5对侧皮瓣看起来是最大的,在背侧视图中呈现椭圆形轮廓。所有的新标本在保存时均显示一个单独的、长、在中部附着的、不分节的尾刺。除前附肢外,尾刺几乎与身体一样长。躯干每节包括一个轴部和一对侧向的、叠瓦状的叶,其具有褶皱结构,解释为背部的鳃。标本有从轴部伸出的次三角形凸起,被解释为粗壮的、叶足形的肢。在完整的标本中,凸起部分连接到轴部的瘤点区域,这也是其他寒武纪叶足动物的特征。虽然宣扬爪虫具有独特的形态组合特征,但其若干特征在不同程度上也被寒武纪叶足动物诸如啰哩山虫属、异虫属、微网虫属、爪网虫属、怪诞虫属以及现生栉蚕属等具有。这些特征包括拥有(1)不分节的叶状足;(2)环形的肌肉组织;(3)带刺的附肢;(4)横向的褶皱与成排的瘤点交替。然而,宣扬爪虫提供了双肢型节肢动物可能起源于具叶足的动物祖先的形态学证据,从而产生了像马尔拉虫属这样缺乏背部肋叶的分类单元,在双肢型节肢动物的进化枝分析中占据了原始地位。在这种情况下,鳃叶和叶足在节肢化过程中会结合在一起,形成双肢。宣扬爪虫揭示的叶足动物与双肢型节肢动物的同源性表明,叶足动物构成了一个并系群,节肢类群由此产生。


Taxonomy

Phylum: Arthropoda

Class: Dinocaridida

Order: uncertain

Family: uncertain

Genus: Kerygmachela

Specie: K.kierkegaardi

Description: 

The ancient creature measured between one to ten inches and is flanked by 11 wrinkly flaps on both sides of the body. The spiny frontal appendages suggests that Kerygmachela may have been a predator; however, fossils indicate a total size of approximately 175 mm and, with a relatively small mouth, suggest that it would have been restricted to very small prey. The predator also sported a round head and an elongated tail spine. The head forms a rounded anterior lobe extending between the frontal appendages. The head of Kerygmachela possess a pair of well-developed frontal appendages which correspond to those of other dinocaridids and siberiid lobopodians. Each of them terminated with a series of long spines. A pair of sessile, slit-like compound eyes were located slightly behind the base of these appendages. At the base of the frontal appendages are structures interpreted as eyes, based on both their position and preservation, with distinctive relief and high reflectivity similar to the preservation of eyes in arthropods from the Burgess Shale. Their outline is reminiscent of the kidney- or sickle-shaped eye lobes of trilobites. The eyes are situated ventrolaterally, because they are best delineated in ventral specimens where mouth structures and rostral spines are most visible. In dorsal specimens, the epidermal annulations continue over the eye lobes. The anterior half of the eye is located under the posterior part of the frontal appendages. The visual structures seen in K.kierkegaardi represent primitive compound eyes. A small anterior-facing mouth was located below its head and bore a pair of stylet-like structures. The head also possesses a median lobe-like projection that carries a pair of small, possible ocular structures. The body compose of 11 segments indicated by 4 dorsal turberculates on each of them, associated with 11 pairs of lateral flaps with dorsal gill-like structure, along with 11 pairs of small legs (lobopods) located just below the flaps. The body ends with a single, unsegmented tail spine which was formerly thought to be a pair of cerci. Internally, Kerygmachela possesses a well-developed pharynx and a midgut with 8 pairs of arthropod-like digestive glands. The brain compose of only protocerebrum (the frontalmost cerebral ganglion) with ramified nerves extended to the median lobe, frontal appendages and eyes. Eleven rows of tubercles are present in the axial region, corresponding to each set of lateral flaps, with four tubercles present in each row. The tubercles become more prominent posteriorly. The central two tubercles are larger than the outer ones and become more widely spaced posteriorly, eventually becoming almost superimposed on the lateral ones in the distal region. The lateral flaps appear successively smaller rearward in the holotype. In the new material, the fourth and fifth pair of lateral flaps appear to be largest, rendering an oval outline in dorsal view. All new specimens show a single, long, medially attached, and unsegmented tail spine, when preserved. The tail spine is almost as long as the body, excluding the frontal appendages. Each segment of the main body is composed with an axial region and a pair of lateral, imbricated lobes that bear wrinkled structures interpreted as gills on the dorsal surface. Specimens exhibit sub-triangular bulges projecting later-ally from the axial region. These bulges are interpreted as stout, lobopod-like limbs. In the complete specimen, the bulges connect to the tubercled units of the axial region,a characteristic of other Cambrian lobopods.

Although Kerygmachela shows a unique combination of morphological features, several of its characters are also possessed in varying degrees by lobopod-like Cambrian animals such as Luolishania, Xenusion, Microdictyon, Onychodictyon, Hallucigenia as well as the Recent Peripatus. These characters include the possession of (1) unsegmented, lobopod limbs; (2) circular body musculature ; (3) appendages with spines; and (4) alternating axial units of transverse wrinkling and rows of tubercles. Kerygmachela, however, provides morphological evidence that the biramous arthropods may be derived from a lobopodous ancestor, giving rise to a taxon like Marrella that lacks dorsal pleurae and occupies a primitive position in cladistic analyses of biramous arthropods. In this case, the gill-lobe and the lobopod would be united during arthropodization to form the biramous limb. The homology of the lobopod and biramous arthropod limbs implied by Kerygmachela suggests that lobopod animals constitute a paraphyletic stem-group assemblage from which arthropodized taxa arose.


年龄和产地

时代:寒武系第二统第三阶,内华达虫化石带

主要产地: 北格陵兰位于富兰克林盆地南缘的西里斯帕斯特生物群(布恩组泥岩段)


Age & Localities

Age: Cambrian Series 2, Stage 3, Nevadella trilobite Biozone

Principal localities: The Sirius Passet fauna (Mudstone-dominated Member of Buen Formation), in the southern margin of the Franklinian Basin, North of Greenland


Reference:

Graham Budd,1993.A Cambrian gilled lobopod from Greenland.Nature volume 364, pp.709–711.

Graham E. Budd,1998.The morphology and phylogenetic significance of Kerygmachela kierkegaardi Budd (Buen Formation,Lower Cambrian, N Greenland).Transactions of the Royal Society of Edinburgh: Earth Sciences,volume 89, pp.249-290.

Jianni Liu, Jason A. Dunlop,2013.Cambrian lobopodians: A review of recent progress in our understanding of their morphology and evolution.Palaeogeography,Volume 398,pp.4-15.

Tae-Yoon S. Park,2018.Brain and eyes of Kerygmachela reveal protocerebral ancestry of the panarthropod head.Nature Communications volume 9,, Article number: 1019.



Copyright © 2022 Department of Geology, Northwest University Made in allwww<易网>