The Changing Shape of Plant Cells: Transformations During Cell Proliferation

Shapes of ideal cells can be inspected for the dynamic, or gnomonic,feature of producing daughter cells of the same shape. Suchfeatures can be found for (a) elongating epidermal cells, (b)isdiametrically enlarging epidermal cells, (c) elongating parenchymatouscells and (d) parenchymatous cells enlarging in three dimensions.Since each cell passes through a series of changes to finallyassume the form of the parental cell, a gnomonic cell must passthrough a gnomonic sequence of shapes during the cell cycle.A model tissue composed of gnomonic cells has complete stabilityof form through subsequent generations. Each of six parameters of ideal cells can be inspected in realcells in order to evaluate the effects of deviations from theideal on the stability of tissue pattern. (1) Cell plates ofreal and ideal cells do not expand for one generation. (2) Theangles in vertices of real cells shift over three cell cyclesfrom 170.1° to 137.3° to 124.0°, values close tothe expected set of 163°, 133° and 120° (3) Cellplates of real cells are not perpendicular to the longitudinalaxis of the cell. (4) Real cells do not divide synchronouslyas do ideal cells. (5) Real cells do not divide equally in halfas do ideal cells. (6) Finally, ideal cells have the same durationof the cell cycle whereas real cells have cycle times inverselyrelated to the initial size of the cell. It appears that a population of meristematic cells do not adhereto the restrictions of ideal cells, and consequently a significantamount of variance of form is added at each generation. Thereare two compensating mechanisms, one to hold size variationin check and one to keep shape deviations under control. Becauseof the probabilistic nature of cell division, cells increasein volume at various rates while the cell edges of all cellsexpand at a constant rate, indicating that the latter is theprimary element of growth while facet area and cell volume increasein dimension only for accommodation. Cell shape, gnomonic cells, Aponogeton elongatus, Lupinus alba     

Soft‐tissue imprints in fossil and Recent cephalopod septa and septum formation

Several soft‐tissue imprints and attachment sites have been discovered on the inside of the shell wall and on the apertural side of the septum of various fossil and Recent ectocochleate cephalopods. In addition to the scars of the cephalic retractors, steinkerns of the body chambers of bactritoids and some ammonoids from the Moroccan and the German Emsian (Early Devonian) display various kinds of striations; some of these striations are restricted to the mural part of the septum, some start at the suture and terminate at the anterior limit of the annular elevation. Several of these features were also discovered in specimens of Mesozoic and Recent nautilids. These structures are here interpreted as imprints of muscle fibre bundles of the posterior and especially the septal mantle, blood vessels as well as the septal furrow. Most of these structures were not found in ammonoids younger than Middle Devonian. We suggest that newly formed, not yet mineralized (or only slightly), septa were more tightly stayed between the more numerous lobes and saddles in more strongly folded septa of more derived ammonoids and that the higher tension in these septa did not permit soft‐parts to leave imprints on the organic preseptum. It is conceivable that this permitted more derived ammonoids to replace the chamber liquid faster by gas and consequently, new chambers could be used earlier than in other ectocochleate cephalopods, perhaps this process began even prior to mineralization. This would have allowed faster growth rates in derived ammonoids.     

The annual cycle in body weight of small mammals from the Transvaal, South Africa, as an adaptation to a subtropical seasonal environment

Seasonal breeding of non-hibernating small mammals is generally associated with a reduction in body weight during the non-breeding period. In aseasonal breeders and in exceptional situations, when winter breeding occurs, this pattern cannot be found.
The reduction in body weight is thought to be a means to reduce energy requirements during the harsh non-breeding season that can either be winter, in the Holarctic, or the dry season in the Transvaal highveld.
The controlling mechanism in the strongly seasonal subtropical environment in southern Africa seems to be photoperiod as in small mammals from the northern hemisphere.
Since a general agreement in body weight changes was found in rodents and shrews from both areas, further similarities in adaptations to strongly seasonal environments in the subtropics are expected.
For the first time it is shown that the adaptive responses of small mammals to unfavourable seasons are similar in the Holarctic and seasonal subtropical areas.