Schneider Nanette Y, Gurovich Yamila
Centre des Sciences du Goût et de l'Alimentation (CSGA), UMR 6265 CNRS, 1324 INRA, Université de Bourgogne-Franche-Comté, Dijon, France.
CONICET y Centro de Investigación Esquel de Montaña y Estepa Patagonica (CIEMEP) Laboratorio de Investigaciones en Evolución y Biodiversidad (LIEB), Universidad Nacional de La Patagonia SJB (UNP), Esquel, Chubut, Argentina.
J Anat. 2017 Jul;231(1):59-83. doi: 10.1111/joa.12621.
Newborn marsupials can be arranged into three grades of developmental complexity based on their external form, as well as based on their organ systems and their cytology. The dasyurids are considered the least developed marsupials at birth, while didelphids and peramelids are intermediate, and macropods are the most developed. Currently there is still little information on caenolestid and microbiotherid development at birth. Developmental stages can be graded as G1, G2 and G3, with G1 being the least developed at birth, and G3 the most developed. Marsupials are also characterized by having an extremely developed craniofacial region at birth compared with placentals. However, the facial region is also observed to vary in development between different marsupial groups at birth. The oral shield is a morphological structure observed in the oral region of the head during late embryological development, which will diminish shortly after birth. Morphological variation of the oral shield is observed and can be arranged by developmental complexity from greatly developed, reduced to vestigial. In its most developed state, the lips are fused, forming together with the rhinarium, a flattened ring around the buccal opening. In this study, we examine the external oral shield morphology in different species of newborn marsupials (dasyurids, peramelids, macropods and didelphids), including the newborn monito del monte young (Dromiciops gliroides - the sole survivor of the order Microbiotheria). The adaptive value of the oral shield structure is reviewed, and we discuss if this structure may be influenced by developmental stage of newborn, pouch cover, species relatedness, or other reproductive features. We observe that the oral shield structure is present in most species of Marsupialia and appears to be exclusively present in this infraclass. It has never been described in Monotremata or Eutherians. It is present in unrelated taxa (e.g. didelphids, dasyurids and microbiotherids). We observe that a well-developed oral shield may be related to ultra altricial development at birth, large litter size (more than two), and is present in most species that lack a pouch in reproductive adult females or have a less prominent or less developed pouch with some exceptions. We try to explore the evolution of the oral shield structure using existing databases and our own observations to reconstruct likely ancestral character states that can then be used to estimate the evolutionary origin of this structure and if it was present in early mammals. We find that a simple to develop oral shield structure (type 2-3) may have been present in marsupial ancestors as well as in early therians, even though this structure is not present in the extant monotremes. This in turn may suggest that early marsupials may have had a very simple pouch or lacked a pouch as seen in some living marsupials, such as some dasyurids, didelphids and caenolestids. The study's results also suggest that different morphological stages of the oral shield and hindlimb development may be influenced by species size and reproductive strategy, and possibly by yet unknown species-specific adaptations.
新生有袋动物可根据其外部形态、器官系统及细胞学特征分为发育复杂性的三个等级。袋鼬科动物被认为是出生时发育最不完善的有袋动物,而负鼠科和袋狸科动物处于中间水平,袋鼠科动物则是发育最完善的。目前关于袋鼹科和微兽科动物出生时发育情况的信息仍然很少。发育阶段可分为G1、G2和G3级,G1级在出生时发育最不完善,G3级最完善。与胎盘类动物相比,有袋动物出生时颅面部区域也极其发达。然而,出生时不同有袋动物群体的面部区域发育也存在差异。口盾是胚胎发育后期在头部口腔区域观察到的一种形态结构,出生后不久就会消失。观察到口盾存在形态变异,可根据发育复杂性排列为从高度发达、退化到残留。在其最发达状态下,嘴唇融合,与鼻镜一起形成围绕口腔开口的扁平环。在本研究中,我们检查了不同种类新生有袋动物(袋鼬科、袋狸科、袋鼠科和负鼠科)的外部口盾形态,包括新生的山猴(智利山猴——微兽目唯一的幸存者)。回顾了口盾结构的适应价值,并讨论了该结构是否可能受新生动物发育阶段、育儿袋覆盖物、物种亲缘关系或其他生殖特征的影响。我们观察到口盾结构存在于大多数有袋动物物种中,并且似乎仅存在于这个下纲中。在单孔目或真兽类中从未有过描述。它存在于不相关的分类群中(如负鼠科、袋鼬科和微兽科)。我们观察到发育良好的口盾可能与出生时的超早产发育、产仔数多(超过两个)有关,并且存在于大多数成年雌性生殖时没有育儿袋或育儿袋不太突出或发育不太完善的物种中,但有一些例外。我们试图利用现有数据库和我们自己的观察结果来探索口盾结构的进化,以重建可能的祖先特征状态,然后用于估计该结构的进化起源以及它是否存在于早期哺乳动物中。我们发现,一种易于发育的口盾结构(2 - 3型)可能存在于有袋动物祖先以及早期兽类中,尽管这种结构在现存的单孔目中不存在。这反过来可能表明早期有袋动物可能有一个非常简单或者像一些现存有袋动物(如一些袋鼬科、负鼠科和袋鼹科动物)那样没有育儿袋。该研究结果还表明,口盾和后肢发育的不同形态阶段可能受物种大小和生殖策略的影响,也可能受尚未知晓的物种特异性适应的影响。