Rewriting the rules governing high intensity interactions of light with matter.

The trajectory of discovery associated with the study of high-intensity nonlinear radiative interactions with matter and corresponding nonlinear modes of electromagnetic propagation through material that have been conducted over the last 50 years can be presented as a landscape in the intensity/quantum energy [I-hω] plane. Based on an extensive series of experimental and theoretical findings, a universal zone of anomalous enhanced electromagnetic coupling, designated as the fundamental nonlinear domain, can be defined. Since the lower boundaries of this region for all atomic matter correspond to hω ~ 10(3) eV and I ≈ 10(16) W cm(-2), it heralds a future dominated by x-ray and γ-ray studies of all phases of matter including nuclear states. The augmented strength of the interaction with materials can be generally expressed as an increase in the basic electromagnetic coupling constant in which the fine structure constant α → Z(2)α, where Z denotes the number of electrons participating in an ordered response to the driving field. Since radiative conditions strongly favoring the development of this enhanced electromagnetic coupling are readily produced in self-trapped plasma channels, the processes associated with the generation of nonlinear interactions with materials stand in natural alliance with the nonlinear mechanisms that induce confined propagation. An experimental example involving the Xe (4d(10)5s(2)5p(6)) supershell for which Z ≅ 18 that falls in the specified anomalous nonlinear domain is described. This yields an effective coupling constant of Z(2)α ≅ 2.4 > 1, a magnitude comparable to the strong interaction and a value rendering as useless conventional perturbative analyses founded on an expansion in powers of α. This enhancement can be quantitatively understood as a direct consequence of the dominant role played by coherently driven multiply-excited states in the dynamics of the coupling. It is also conclusively demonstrated by an abundance of data that the utterly peerless champion of the experimental campaign leading to the definition of the fundamental nonlinear domain was excimer laser technology. The basis of this unique role was the ability to satisfy simultaneously a triplet (ω, I, P) of conditions stating the minimal values of the frequency ω, intensity I, and the power P necessary to enable the key physical processes to be experimentally observed and controllably combined. The historical confluence of these developments creates a solid foundation for the prediction of future advances in the fundamental understanding of ultra-high power density states of matter. The atomic findings graciously generalize to the composition of a nuclear stanza expressing the accessibility of the nuclear domain. With this basis serving as the launch platform, a cadenza of three grand challenge problems representing both new materials and new interactions is presented for future solution; they are (1) the performance of an experimental probe of the properties of the vacuum state associated with the dark energy at an intensity approaching the Schwinger/Heisenberg limit, (2) the attainment of amplification in the γ-ray region (~1 MeV) and the discovery of a nuclear excimer, and (3) the determination of a path to the projected super-heavy nuclear island of stability.

Formation of host-guest complexes of ß-cyclodextrin and perfluorooctanoic acid.

Structural characterization and dynamic properties of solid-state inclusion complexes of ß-cyclodextrin (ß-CD) with perfluorooctanoic acid (PFOA) were investigated by (19)F/(13)C solid-state and (19)F/(1)H solution NMR spectroscopy. The complexes in the solid state were prepared using dissolution and slow cool methods, where thermal analyses (DSC and TGA), PXRD, and FT-IR results provided complementary support that inclusion complexes were formed between ß-CD and PFOA with variable stoichiometry and inclusion geometry. (19)F DP (direct polarization) and (13)C CP (cross-polarization) with magic-angle spinning (MAS) solids NMR, along with (19)F/(1)H solution NMR were used to characterize the complexes in the solid and solution phases, respectively. The dynamics of the guest molecules in the inclusion complexes (ICs) were studied using variable temperature (VT) (19)F DP/MAS NMR experiments in the solid state. The guest molecules were observed to be in several different molecular environments, providing strong evidence of variable host-guest stoichiometry and inclusion geometry, in accordance with the preparation method of the complex and the conformational preference of PFOA. It was concluded from PXRD that ß-CD and PFOA form inclusion complexes with "channel-type" structures. Variable spin rate (VSR) (19)F DP/MAS NMR was used to assess the phase purity of the complexes, and it was revealed that slow cooling resulted in relatively pure phases. In the solution state, (1)H and (19)F NMR complexation-induced chemical shifts (CISs) of ß-CD and PFOA, respectively, provided strong support for the formation of 1:1 and 2:1 ß-CD/PFOA inclusion complexes. The dynamics of the guest molecule in the ß-CD/PFOA complexes in D(2)O solutions were probed using VT (19)F NMR and revealed some guest conformational and exchange dynamics as a function of temperature and the relative concentrations of the host and guest.

The pea Sym37 receptor kinase gene controls infection-thread initiation and nodule development.

Phenotypic characterization of pea symbiotic mutants has provided a detailed description of the symbiosis with Rhizobium leguminosarum bv. viciae strains. We show here that two allelic non-nodulating pea mutants, RisNod4 and K24, are affected in the PsSym37 gene, encoding a LysM receptor kinase similar to Lotus japonicus NFR1 and Medicago truncatula LYK3. Phenotypic analysis of RisNod4 and K24 suggests a role for the SYM37 in regulation of infection-thread initiation and nodule development from cortical-cell division foci. We show that RisNod4 plants carrying an L to F substitution in the LysM1 domain display a restrictive symbiotic phenotype comparable to the PsSym2(A) lines that distinguish 'European' and 'Middle East' Rhizobium leguminosarum bv. viciae strains. RisNod4 mutants develop nodules only in the presence of a 'Middle East' Rhizobium strain producing O-acetylated Nod factors indicating the SYM37 involvement in Nod-factor recognition. Along with the PsSym37, a homologous LysM receptor kinase gene, PsK1, was isolated and characterized. We show that PsK1 and PsSym37 are genetically linked to each other and to the PsSym2 locus. Allelic complementation analyses and sequencing of the extracellular regions of PsSym37 and PsK1 in several 'European' and 'Afghan' pea cultivars point towards PsK1 as possible candidate for the elusive PsSym2 gene.

Developmental genetics and evolution of symbiotic structures in nitrogen-fixing nodules and arbuscular mycorrhiza.

Genetic and molecular mechanisms of development are compared for two major plant-microbe endosymbioses: N(2)-fixing nodules (with rhizobia or actinomycetes Frankia) and arbuscular mycorrhiza (with Glomales fungi). Development from the primordia formed de novo in root tissues is common for all known types of N(2)-fixing nodules. However, their structure varies greatly with respect to: (i) tissue topology (location of vascular bundles is peripherical in legumes or central in non-legumes); (ii) position of nodule primordium (inner or outer cortex in legumes, pericycle in non-legumes); (iii) stability of apical meristem (persistent in the indeterminate nodules, transient in the determinate ones). In addition, legumes vary in ability to form compartments harboring endosymbiotic rhizobia and located intercellularly (infection threads) and intracellularly (symbiosomes). Using pea (Pisum sativum) symbiotic mutants, the nodule developmental program is dissected into a range of spatially and temporarily differentiated steps comprising four sub-programs (development of endosymbiotic compartments; nodule histogenesis; autoregulation of nodulation; bacteroid differentiation). The developmental mutations are suggested in some cases to reverse the endosymbiotic system into the morphologically simpler forms some of which may correspond to the ancestral stages of nodule evolution. The origin of legume-rhizobial and actinorhizal symbioses is suggested to be based on a set of preadaptations many of which had been evolved in angiosperms during coevolution with arbuscular mycorrhizal fungi (e.g., inter- and intracellular maintenance of symbionts, their control via defence-like reactions and recognition of chitin-like molecules). An analysis of parallel morphological variation in symbiotic mutants and wild-growing legume species enables us to reconstruct the major stages of evolution for N(2)-fixing symbioses.