Maier W
Gegenbaurs Morphol Jahrb. 1987;133(1):123-61.
In most marsupials, the angular process is inflected medially. By using an ontogenetic series of Monodelphis domestica, the development of this characteristic structure has been described. In contrast with the eutherian mammals, in marsupials there is retained a close connection between the dentale and the tympanicum and goniale; it is well known that these 2 elements of the middle ear are derived from the angulare and prearticulare of the reptilian lower jaw. At the neonatal stage, the dentale and tympanicum are both relatively vertically orientated; during the following 2 weeks, they take an increasingly oblique position, which is primarily caused by the rapid growth of the braincase. Only after the eruption of the first teeth, the ascending ramus of the dentale takes a more and more vertical position, whereas the angular process remains with its tip near the medioventral floor of the tympanic bulla. The bulla shows at this place a rectangular fenestra which is covered by a membrane of loose connective tissue; the tip of the angular process, which is always free of muscular insertions, maintains contacts with this fenestra throughout life. During juvenile and adult life stages, the process becomes somewhat removed from the fenestra for obvious reasons, but at a gape of about 40 to 50 degrees it inevitably must touch the "inferior tympanic membrane" and possibly also the tympanic ring. It is speculated that the relationship between the angular process and the tympanic bulla represents a specific form-function complex for sound transmission, which may be a modified retention from archaic mammalian conditions. Further details of the ontogenetic development of the tympanic region have been described which may be of some relevance for the evolutionary morphology of mammals: The tympanic process of the petrosal, which fixes the posterior end of the tympanic ring, is formed by 'Zuwachsknochen' (additional bone) but not by cartilage. The styloid process remains cartilaginous throughout life: its free tip ends in the lateral wall of the tympanic cavity and it is closely connected with the collum mallei and the posterior end of the tympanicum; it guides the chorda tympani and may therefore be homologous with the cartilage of Spence. The cartilage of Paauw is interpreted in terms of functional morphology. A model of evolutionary transformation of the dentale-tympanicum complex in mesozoic mammals in outlined on the basis of the ontogenetic findings in Monodelphis and other didelphid and dasyurid marsupials.
在大多数有袋类动物中,角突向内侧弯曲。通过使用家短尾负鼠的个体发育系列,已经描述了这种特征结构的发育过程。与真兽类哺乳动物不同,在有袋类动物中,齿骨与鼓骨和角节之间保持着紧密的联系;众所周知,中耳的这两个部分源自爬行动物下颌的隅骨和前关节骨。在新生儿阶段,齿骨和鼓骨都相对垂直定向;在接下来的两周内,它们逐渐倾斜,这主要是由于脑壳的快速生长所致。只有在第一颗牙齿萌出后,齿骨的升支才越来越垂直,而角突的尖端仍靠近鼓泡的内侧腹侧底部。鼓泡在这个位置有一个矩形的窗孔,被一层疏松结缔组织膜覆盖;角突的尖端始终没有肌肉附着,终生与这个窗孔保持接触。在幼年和成年阶段,由于明显的原因,这个过程与窗孔有些分离,但在大约40到50度的张口时,它不可避免地会接触到“下鼓膜”,也可能接触到鼓膜环。据推测,角突与鼓泡之间的关系代表了一种用于声音传播的特定形式-功能复合体,这可能是从古老哺乳动物状态保留下来的一种变体。已经描述了鼓室区域个体发育的进一步细节,这可能与哺乳动物的进化形态学有一定关联:固定鼓膜环后端的岩骨鼓突是由“附加骨”形成的,而不是由软骨形成的。茎突终生保持软骨状态:其游离端终止于鼓室的侧壁,与锤骨颈和鼓骨的后端紧密相连;它引导鼓索神经,因此可能与斯彭斯软骨同源。帕乌软骨是根据功能形态学来解释的。基于家短尾负鼠以及其他双门齿目和袋鼬科有袋类动物的个体发育研究结果,勾勒出了中生代哺乳动物齿骨-鼓骨复合体的进化转变模型。