The basic body plan of arthropods: insights from evolutionary morphology and developmental biology

1997 ◽  
Vol 10 (3) ◽  
pp. 353 ◽  
Author(s):  
J. Zrzavý ◽  
P. Štys
Development ◽  
2014 ◽  
Vol 141 (24) ◽  
pp. 4649-4655 ◽  
Author(s):  
N. Irie ◽  
S. Kuratani

1976 ◽  
Vol 11 (2) ◽  
pp. 74-77
Author(s):  
Harold J. Morowitz
Keyword(s):  

2017 ◽  
Vol 284 (1862) ◽  
pp. 20171348 ◽  
Author(s):  
Renee S. Hoekzema ◽  
Martin D. Brasier ◽  
Frances S. Dunn ◽  
Alexander G. Liu

The late Ediacaran soft-bodied macroorganism Dickinsonia (age range approx. 560–550 Ma) has often been interpreted as an early animal, and is increasingly invoked in debate on the evolutionary assembly of eumetazoan body plans. However, conclusive positive evidence in support of such a phylogenetic affinity has not been forthcoming. Here we subject a collection of Dickinsonia specimens interpreted to represent multiple ontogenetic stages to a novel, quantitative method for studying growth and development in organisms with an iterative body plan. Our study demonstrates that Dickinsonia grew via pre-terminal ‘deltoidal’ insertion and inflation of constructional units, followed by a later inflation-dominated phase of growth. This growth model is contrary to the widely held assumption that Dickinsonia grew via terminal addition of units at the end of the organism bearing the smallest units. When considered alongside morphological and behavioural attributes, our developmental data phylogenetically constrain Dickinsonia to the Metazoa, specifically the Eumetazoa plus Placozoa total group. Our findings have implications for the use of Dickinsonia in developmental debates surrounding the metazoan acquisition of axis specification and metamerism.


Author(s):  
Eliot Goldfinger

There is a basic body plan common to most of the animals presented in this book. At its most obvious, they all have a head, a body, and four limbs. Most are four-legged and stand on all fours, and are described as having front limbs and rear limbs. The front limb is anatomically equivalent to the arm and hand in humans and primates, and the rear limb to the human lower limb. The animals in this book are surprisingly similar in many ways. The head is connected to the rib cage by the neck vertebrae and the rib cage is connected to the pelvis by the lumbar vertebrae. The two front limbs are connected to the rib cage, and the two rear limbs are connected to the pelvis. These units move in relation to one another, establishing the stance, or pose, of an animal. Animals differ primarily in the shape and relative proportions of these structural units, in the position of the wrist, heel, and toe bones when standing and walking, and by the number of their toes. An animal can be visualized as being constructed of a series of simplified, three-dimensional, somewhat geometric volumes (head, forearm, thigh). Each of these volumes has one dimension that is longer than the others. A line projected through the center of the mass of this volume on its longest dimension is called its axis (plural, axes). For the most part, especially in the limbs, these axes follow the skeleton, so that a line drawn through the long dimension of a bone is on, or close to, the axis of the volume of that region (for example, the position of the radius is close to the axis of the forearm). One of the more confusing regions of the body is the volume of the upper arm. The humerus (upper arm bone) is mostly deeply buried in muscle, and lies toward the front of this muscle mass, with the massive triceps muscle located at its rear.


Nature ◽  
1984 ◽  
Vol 310 (5972) ◽  
pp. 10-11 ◽  
Author(s):  
Gary Struhl

2001 ◽  
Vol 356 (1414) ◽  
pp. 1599-1613 ◽  
Author(s):  
Thomas F. Schilling ◽  
Robert D. Kinght

All chordates share a basic body plan and many common features of early development. Anteroposterior (AP) regions of the vertebrate neural tube are specified by a combinatorial pattern of Hox gene expression that is conserved in urochordates and cephalochordates. Another primitive feature of Hox gene regulation in all chordates is a sensitivity to retinoic acid during embryogenesis, and recent developmental genetic studies have demonstrated the essential role for retinoid signalling in vertebrates. Two AP regions develop within the chordate neural tube during gastrulation: an anterior ‘forebrain–midbrain’ region specified by Otx genes and a posterior ‘hindbrain–spinal cord’ region specified by Hox genes. A third, intermediate region corresponding to the midbrain or midbrain–hindbrain boundary develops at around the same time in vertebrates, and comparative data suggest that this was also present in the chordate ancestor. Within the anterior part of the Hox –expressing domain, however, vertebrates appear to have evolved unique roles for segmentation genes, such as Krox–20 , in patterning the hindbrain. Genetic approaches in mammals and zebrafish, coupled with molecular phylogenetic studies in ascidians, amphioxus and lampreys, promise to reveal how the complex mechanisms that specify the vertebrate body plan may have arisen from a relatively simple set of ancestral developmental components.


Development ◽  
1992 ◽  
Vol 116 (Supplement) ◽  
pp. NP-NP

Gastrulation is the developmental process, involving extensive cell reorganizations, which results in the formation of the mesoderm and gut endoderm of the embryo. The prefix gastr- in fact means ‘stomach’, which is perhaps both a reference to the shape of the gastrula stage of miolecithal eggs (e.g. sea urchin, Amphioxus) and to the fact that the endoderm, which lines the digestive tube, arises during gastrulation. Its importance was eulogised by Lewis Wolpert's famous statement that ‘it is not birth, marriage or death but gastrulation that is truly the most important time in your life’. Not only does the embryo become trilaminar, but it is also during gastrulation that the basic body plan is laid down, the three axes of the embryo become established and many cells receive the signals that lead them to acquire developmental fates and positional information.


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