Transfinite reductions in orthogonal term rewriting systems

Strongly convergent reduction is the fundamental notion of reduction in infinitary orthogonal term rewriting systems (OTRSs). For these we prove the Transfinite Parallel Moves Lemma and the Compressing Lemma. Strongness is necessary as shown by counterexamples. Normal forms, which we allow to be infinite, are unique, in contrast to ω-normal forms. Strongly converging fair reductions result in normal forms. In general OTRSs the infinite Church-Rosser Property fails for strongly converging reductions. However for Böhm reduction (as in Lambda Calculus, subterms without head normal forms may be replaced by ⊥) the infinite Church-Rosser property does hold. The infinite Church-Rosser Property for non-unifiable OTRSs follows. The top-terminating OTRSs of Dershowitz c.s. are examples of non-unifiable OTRSs

Infinitary lambda calculus

In a previous paper we have established the theory of transfinite reduction for orthogonal term rewriting systems. In this paper we perform the same task for the lambda calculus. From the viewpoint of infinitary rewriting, the Böhm model of the lambda calculus can be seen as an infinitary term model. In contrast to term rewriting, there are several different possible notions of infinite term, which give rise to different Böhm-like models, which embody different notions of lazy or eager computation

Syntactic definitions of undefined: On defining the undefined

In the lambda-calculus, there is a standard notion of what terms should be considered to be “undefined”: the unsolvable terms. There are various equivalent characterisations of this property of terms. We attempt to find a similar notion for orthogonal term rewrite systems. We find that in general the properties of terms analogous to the various characterisations of solvability differ. We give two axioms that a notion of undefinedness should satisfy, and explore some of their consequences. The axioms lead to a concept analogous to the Böhm trees of the λ-calculus. Each term has a unique B5hm tree, and the set of such trees forms a domain which provides a denotational semantics for the rewrite system. We consider several particular notions of undefinedness satisfying the axioms, and compare them

Formation and Shaping of the Antirrhinum Flower through Modulation of the CUP Boundary Gene

Boundary domain genes, expressed within or around organ primordia, play a key role in the formation, shaping, and subdivision of planar plant organs, such as leaves. However, the role of boundary genes in formation of more elaborate 3D structures, which also derive from organ primordia, remains unclear. Here we analyze the role of the boundary domain gene CUPULIFORMIS (CUP) in formation of the ornate Antirrhinum flower shape. We show that CUP expression becomes cleared from boundary subdomains between petal primordia, most likely contributing to formation of congenitally fused petals (sympetally) and modulation of growth at sinuses. At later stages, CUP is activated by dorsoventral genes in an intermediary region of the corolla. In contrast to its role at organ boundaries, intermediary CUP activity leads to growth promotion rather than repression and formation of the palate, lip, and characteristic folds of the closed Antirrhinum flower. Intermediary expression of CUP homologs is also observed in related sympetalous species, Linaria and Mimulus, suggesting that changes in boundary gene activity have played a key role in the development and evolution of diverse 3D plant shapes

Shaping of a three-dimensional carnivorous trap through modulation of a planar growth mechanism

Leaves display a remarkable range of forms, from flat sheets with simple outlines to cup-shaped traps. Although much progress has been made in understanding the mechanisms of planar leaf development, it is unclear whether similar or distinctive mechanisms underlie shape transformations during development of more complex curved forms. Here, we use 3D imaging and cellular and clonal analysis, combined with computational modelling, to analyse the development of cup-shaped traps of the carnivorous plant Utricularia gibba. We show that the transformation from a near-spherical form at early developmental stages to an oblate spheroid with a straightened ventral midline in the mature form can be accounted for by spatial variations in rates and orientations of growth. Different hypotheses regarding spatiotemporal control predict distinct patterns of cell shape and size, which were tested experimentally by quantifying cellular and clonal anisotropy. We propose that orientations of growth are specified by a proximodistal polarity field, similar to that hypothesised to account for Arabidopsis leaf development, except that in Utricularia, the field propagates through a highly curved tissue sheet. Independent evidence for the polarity field is provided by the orientation of glandular hairs on the inner surface of the trap. Taken together, our results show that morphogenesis of complex 3D leaf shapes can be accounted for by similar mechanisms to those for planar leaves, suggesting that simple modulations of a common growth framework underlie the shaping of a diverse range of morphologies