Organogenesis of the female reproductive structure of Myrica pensylvanica

1980 ◽  
Vol 58 (18) ◽  
pp. 2001-2006 ◽  
Author(s):  
Alastair D. Macdonald
Keyword(s):  
Second Order ◽  
Reproductive Structure ◽  
Third Order ◽  
Inflorescence Axis ◽  
Myrica Pensylvanica

The female reproductive structure of Myrica pensylvanica comprises a gynoecium and four second-order inflorescence bracts. The gynoecium terminates the second-order inflorescence axis. The receptacle, comprising second- and third-order inflorescence axis tissue, forms most of the gynoecial wall and gives rise to the wax-secreting papillae. Papillae, which are vascularized, are not initiated in the same manner as trichomes. An hypothesis is formulated whereby papillae may be homologized to inflorescence bracts.

Inception of the cupule of Quercus macrocarpa and Fagus grandifolia

1979 ◽  
Vol 57 (17) ◽  
pp. 1777-1782 ◽  
Author(s):  
Alastair D. Macdonald
Keyword(s):  
Female Flower ◽  
Fagus Grandifolia ◽  
Second Order ◽  
The Other ◽  
Third Order ◽  
Quercus Macrocarpa ◽  
First Order ◽  
Female Inflorescence ◽  
Inflorescence Axis ◽  
Morphological Nature

The female inflorescence of Fagus grandifolia comprises two flowers; one flower terminates the first-order inflorescence axis, the other flower terminates the second-order inflorescence axis. Each flower is flanked by two cupular valves each of which arise in the axil of a bract. The two valves flanking the flower terminating the first-order inflorescence axis represent second-order inflorescence axes and the two valves flanking the flower terminating the second-order inflorescence axis represent third-order inflorescence axes. The four valves remain discrete. Each female flower of Quercus macrocarpa terminates a second-order inflorescence axis and is surrounded by a continuous cupule. The cupule first forms as two primordia in the axils of each of the two transversal second-order bracts. These cupular primordia represent third-order inflorescence branches. The cupule primordia become continuous about the pedicel by meristem extension. The cupules of Fagus and Quercus are homologous to the extent that they are modified axes of the inflorescence. This serves as a model to interpret the morphological nature of the fagaceous cupule.

Development of the female flower and gynecandrous partial inflorescence of Myrica californica

1979 ◽  
Vol 57 (2) ◽  
pp. 141-151 ◽  
Author(s):  
Alastair D. Macdonald
Keyword(s):  
Fourth Order ◽  
Female Flower ◽  
Second Order ◽  
Third Order ◽  
First Order ◽  
Unique Structure ◽  
Inflorescence Axis ◽  
Definition Of ◽  
Fifth Order ◽  
Partial Inflorescence

Organogenesis of the female flower and gynecandrous partial inflorescence is described. Approximately 25 first-order inflorescence bracts are formed in an acropetal sequence. A second-order inflorescence axis, the partial inflorescence, develops in the axil of each bract. Third-, fourth-, and fifth-order axes arise in the axils of second-, third-, and fourth-order bracts. A gynoecium terminates a second-order axis and sometimes a distal third-order axis. A gynoecium consists of two stigmas and one basal, unitegmic, orthotropous ovule. The wall enclosing the ovule, the circumlocular wall, is comprised distally of gynoecial tissue and proximally of tissue of the inflorescence axis and its appendages. The latter portion of the wall is formed by zonal growth. Androecial members, formed proximal to the gynoecium on the partial inflorescence, are carried onto the circumlocular wall by zonal growth. A stamen may develop from the last-formed primordium before gynoecial inception or from a potentially stigmatic primordium. The papillae of the flower and fruit arise as emergences and from potentially bracteate, axial, and staminate primorida during the development of the circumlocular wall. The term circumlocular wall is used in a neutral sense to describe this unique structure. Since the gynoecium is composed of gynoecial appendages and inflorescence axis and appendages, a functional definition of gynoecium must be expanded to include any tissue, including an inflorescence, that surrounds the ovule(s) and forms the fruit(s).

Bulk Contributions Modulate the Sum-Frequency Generation Spectra of Interfacial Water on Model Sea-Spray Aerosols

2018 ◽  
Author(s):  
Sandeep K. Reddy ◽  
Raphael Thiraux ◽  
Bethany A. Wellen Rudd ◽  
Lu Lin ◽  
Tehseen Adel ◽  
...  
Keyword(s):  
Single Layer ◽  
Sum Frequency Generation ◽  
Second Order ◽  
Interfacial Structure ◽  
Sea Spray ◽  
Third Order ◽  
Systematic Analysis ◽  
Sum Frequency ◽  
Structure Of Water ◽  
Frequency Generation

Vibrational sum-frequency generation (vSFG) spectroscopy is used to determine the molecular structure of water at the interface of palmitic acid monolayers. Both measured and calculated spectra display speci c features due to third-order contributions to the vSFG response which are associated with nite interfacial electric potentials. We demonstrate that theoretical modeling enables to separate the third-order contributions, thus allowing for a systematic analysis of the strictly surface-sensitive, second-order component of the vSFG response. This study provides fundamental, molecular-level insights into the interfacial structure of water in a neutral surfactant system with relevance to single layer bio-membranes and environmentally relevant sea-spray aerosols. These results emphasize the key role that computer simulations can play in interpreting vSFG spectra and revealing microscopic details of water at complex interfaces, which can be difficult to extract from experiments due to the mixing of second-order, surface-sensitive and third-order, bulk-dependent contributions to the vSFG response.

Evidence for general base catalysis by protic solvents in a kinetic study of alcoholyses and hydrolyses of 1-(phenoxycarbonyl)pyridinium ions under both solvolytic and non-solvolytic conditions

2009 ◽  
Vol 74 (1) ◽  
pp. 43-55 ◽  
Author(s):  
Dennis N. Kevill ◽  
Byoung-Chun Park ◽  
Jin Burm Kyong
Keyword(s):  
Second Order ◽  
Base Catalysis ◽  
Substitution Reactions ◽  
Third Order ◽  
Methoxy Derivative ◽  
First Order ◽  
General Base ◽  
Protic Solvents ◽  
Kinetics Of ◽  
Pyridinium Ions

The kinetics of nucleophilic substitution reactions of 1-(phenoxycarbonyl)pyridinium ions, prepared with the essentially non-nucleophilic/non-basic fluoroborate as the counterion, have been studied using up to 1.60 M methanol in acetonitrile as solvent and under solvolytic conditions in 2,2,2-trifluoroethan-1-ol (TFE) and its mixtures with water. Under the non- solvolytic conditions, the parent and three pyridine-ring-substituted derivatives were studied. Both second-order (first-order in methanol) and third-order (second-order in methanol) kinetic contributions were observed. In the solvolysis studies, since solvent ionizing power values were almost constant over the range of aqueous TFE studied, a Grunwald–Winstein equation treatment of the specific rates of solvolysis for the parent and the 4-methoxy derivative could be carried out in terms of variations in solvent nucleophilicity, and an appreciable sensitivity to changes in solvent nucleophilicity was found.

Panicle, spikelet, and floret development in orchardgrass (Dactylis glomerata)

1993 ◽  
Vol 71 (4) ◽  
pp. 523-532 ◽  
Author(s):  
Joanna Fraser ◽  
Eric G. Kokko
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Unique Feature ◽  
Dactylis Glomerata ◽  
Bilateral Symmetry ◽  
Second Order ◽  
Third Order ◽  
First Order ◽  
Lateral Branches ◽  
Scanning Electron

The initial stages of panicle, spikelet, and floret development in field-grown 'Kay' orchardgrass were examined using scanning electron microscopy. Spikelets arose from a complex multilevelled sequence of initiation from branch apices. Spikelets developed indirectly in a two-tiered progression: (i) an acropetal and basipetal sequence of first order, second-order, and third-order inflorescence apices, and (ii) an acropetal development within subclusters of higher-order lateral branch inflorescence apices. The panicle had the unique feature of dorsiventrality as well as bilateral symmetry. The basal apex from first-order, second-order, or third-order apices developed on the same side of the main axis as the first-order apex. The two glumes subtending each spikelet primordium developed alternately and acropetally. Development and initiation of florets within spikelets was basipetal within the panicle, basipetal within clusters and subclusters of spikelets on lateral branches, and acropetal within spikelets. Within florets, paleas developed later than lemmas. Key words: Dactylis glomerata, cocksfoot, scanning electron microscopy, development, panicle.

scholarly journals Probing the Locally Generated Even and Odd Order Nonlinearity in Y–Ba–Cu–O and Tl–Ba–Ca–Cu–O (2212) Microwave Resonators Around <img src="/images/tex/19586.gif" alt="T_{\rm C}">

2013 ◽  
Vol 23 (3) ◽  
pp. 9000105-9000105 ◽  
Author(s):  
Brooke Jeries ◽  
Sean Cratty ◽  
S Remillard
Keyword(s):  
Meissner Effect ◽  
Second Order ◽  
Intermodulation Distortion ◽  
Coaxial Cable ◽  
Superconducting Resonators ◽  
Third Order ◽  
Odd Order ◽  
Similar Temperature Dependence ◽  
Similar Temperature ◽  
Lower Temperature

Spatial scanning of the synchronously generated second- and third-order intermodulation distortion in superconducting resonators uncovers local nonlinearity hot spots, and possible time reversal symmetry breaking, using a simple probe fashioned from coaxial cable. It is clear that even and odd order nonlinearity in these samples do not share the same physical origins, because their temperature and static magnetic field dependences are quite different. 2nd order intermodulation distortion remains strong in these measurements as the temperature continues to drop belowTCto 77 K even though the 3rd order peaks nearTCand becomes smaller at lower temperature as predicted by the nonlinear Meissner effect. Both YBa2Cu3O7and Tl2Ba2CaCu2O8resonators of the same structure exhibit similar temperature dependence in the second order with second order remaining high at lower temperature. The YBa2Cu3O7sample has lower third-order intermodulation distortion with a pronounced peak atTC.

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