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  • 1
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    In:  Blumea - Biodiversity, Evolution and Biogeography of Plants (0006-5196) vol.53 (2008) nr.3 p.549
    Publication Date: 2015-03-06
    Description: A first phylogenetic placement of Petitiocodon based on molecular sequence data from three plastid regions (accD-psa1, rpl16 and trnL-F) is presented, in conjunction with a reassessment of morphology for the genus. Our results do not support an evolutionary affinity between Petitiocodon and Tricalysia (Coffeeae) as suggested by previous studies, but they confirm other research that Petitiocodon and Didymosalpinx are distinct genera. Placement of Petitiocodon in tribe Octotropideae is well-supported on the basis of molecular data and floral and carpological characters.
    Keywords: Octotropideae ; African flora ; accD-psa1 ; rpl16 ; trnL-F ; molecular phylogenetics ; placentation
    Repository Name: National Museum of Natural History, Netherlands
    Type: Article / Letter to the editor
    Format: application/pdf
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  • 2
    Publication Date: 2024-01-12
    Description: A first phylogenetic placement of Petitiocodon based on molecular sequence data from three plastid regions (accD-psa1, rpl16 and trnL-F) is presented, in conjunction with a reassessment of morphology for the genus. Our results do not support an evolutionary affinity between Petitiocodon and Tricalysia (Coffeeae) as suggested by previous studies, but they confirm other research that Petitiocodon and Didymosalpinx are distinct genera. Placement of Petitiocodon in tribe Octotropideae is well-supported on the basis of molecular data and floral and carpological characters.
    Keywords: Octotropideae ; African flora ; accD-PSA1 ; rpl16 ; trnL-F ; molecular phylogenetics ; placentation
    Repository Name: National Museum of Natural History, Netherlands
    Type: info:eu-repo/semantics/article
    Format: application/pdf
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  • 3
    Publication Date: 2024-01-12
    Description: A first phylogenetic placement of Petitiocodon based on molecular sequence data from three plastid regions (accD-psa1, rpl16 and trnL-F) is presented, in conjunction with a reassessment of morphology for the genus. Our results do not support an evolutionary affinity between Petitiocodon and Tricalysia (Coffeeae) as suggested by previous studies, but they confirm other research that Petitiocodon and Didymosalpinx are distinct genera. Placement of Petitiocodon in tribe Octotropideae is well-supported on the basis of molecular data and floral and carpological characters.
    Keywords: Octotropideae ; African flora ; accD-psa1 ; rpl16 ; trnL-F ; molecular phylogenetics ; placentation
    Repository Name: National Museum of Natural History, Netherlands
    Type: info:eu-repo/semantics/article
    Format: application/pdf
    Location Call Number Limitation Availability
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  • 4
    Publication Date: 2024-01-12
    Description: In the 1990s Rubiaceae became a hot spot for systematists, mainly due to the comprehensive treatment of the family by Robbrecht in 1988. Next to the exploration of macromolecular characters to infer the phylogeny, the palynology of Rubiaceae finally received the attention it deserves. This article aims to present a state-of-the-art analysis of the systematic palynology of the family. The range of variation in pollen morphology is wide, and some of the pollen features are not known from other angiosperm taxa; e.g., a looplike or spiral pattern for the position of apertures in pantoaperturate grains. We compiled an online database at the generic level for the major pollen characters and orbicule presence in Rubiaceae. An overview of the variation is presented here and illustrated per character: dispersal unit, pollen size and shape, aperture number, position and type, sexine ornamentation, nexine pattern, and stratification of the sporoderm. The presence/absence and morphological variation of orbicules at the generic level is provided as well. The systematic usefulness of pollen morphology in Rubiaceae is discussed at the (sub)family, tribal, generic, and infraspecific levels, using up-to-date evolutionary hypotheses for the different lineages in the family. The problems and opportunities of coding pollen characters for cladistic analyses are also treated.
    Keywords: Rubiaceae ; pollen morphology ; palynology ; phylogeny
    Repository Name: National Museum of Natural History, Netherlands
    Type: info:eu-repo/semantics/article
    Format: application/pdf
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  • 5
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 96 (1992), S. 7321-7332 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The optothermal detection method has been used to obtain near-infrared spectra of the H2O–CO2 and H2O –HCCH van der Waals molecules in the 3 μm region. For H2O–CO2, the observed vibrational band correlates with the asymmetric O–H stretching vibration of the water monomer and gives a direct measurement of the internal rotation tunneling splitting, from which the height of the associated barrier is estimated. This experimental estimate is compared with results obtained from both a distributed multipole analysis and an ab initio calculation. In the case of H2O –HCCH, three different vibrational bands are observed. Although these spectra are not directly sensitive to the wide amplitude motion in this molecule, they are consistent with the quasiplanar picture suggested by the ab initio calculations. These calculations show the molecule to have a bent equilibrium structure, with a small barrier located at the planar geometry.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 98 (1993), S. 10107-10107 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 98 (1993), S. 3754-3762 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The optothermal detection method has been used to obtain high resolution infrared spectra for both the ν9 and ν11 vibrational bands of Ar-ethylene. Analysis of these spectra reveals that the argon atom lies essentially in the plane of the ethylene, situated next to the carbon–carbon double bond. Although the rigid structure that best fits the measured rotational constants actually places the argon atom 15° out of the ethylene plane, the experimental and theoretical results are more consistent with a planar equilibrium geometry and wide amplitude in-plane and out-of-plane motion of the ethylene sub-unit. In both spectra the transitions appear as doublets, due to the fact that the ethylene sub-unit undergoes internal rotation between equivalent frameworks. Of the possible paths, only internal rotation about the C=C axis is consistent with the data. The barrier to internal rotation is estimated from the tunneling splitting to be 76 cm−1, which is compared with the results of ab initio calculations.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 99 (1993), S. 8585-8598 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Infrared spectra have been obtained for the Ar–C2H2 complex, which include a combination band associated with the low frequency bending mode. These data are used, together with ab initio calculations and the results of previous studies of this system, to construct a two-dimensional Hartree–Fock plus damped dispersion (HFD) intermolecular potential surface corresponding to the C–H stretch excited vibrational state. A high quality SCF surface, which includes ghost orbital corrections, has been used to fix the repulsive part of the potential. The remaining potential parameters were initially estimated with the aid of various combining rules and the collocation technique was used to solve the bound state problem for this potential and to calculate the spectrum of the Ar–C2H2 complex. To obtain good agreement between the calculated and experimental spectra it was necessary to distribute the dispersion interaction over the length of the acetylene subunit. The result is a double minimum potential upon which the complex executes wide amplitude bending motion.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 102 (1995), S. 3993-3999 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Reported here are the first rotationally assigned near-infrared spectra of the ethylene dimer. The vibrational bands observed in this study correlate with ν9 and ν11 of the ethylene monomer, corresponding to C–H stretching motion. The spectral patterns have been identified as due to the vibrational transitions of a symmetric top molecule with D2d symmetry. This structure of the dimer has been predicted by ab initio calculations as the most stable geometry due to the fact that it enables the formation of four equivalent hydrogen bonds. Both vibrational bands show considerable homogeneous broadening corresponding to vibrational predissociation lifetimes of 0.37 and 0.18 ns for ν9 and ν11 excitation, respectively. © 1995 American Institute of Physics.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 103 (1995), S. 7788-7795 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: A rotationally resolved near-infrared spectrum has been obtained for the ethylene–CO2 van der Waals complex. The structure obtained for this complex has the carbon dioxide lying above the plane of the ethylene molecule, with the CO2 axis parallel to this plane. The individual subbands observed in the spectrum are shifted from the expected rigid rotor positions, indicative of internal rotation of the two monomer units within the complex. A double rotor model is presented that accounts for the shifts and provides an estimate of the barrier to internal rotation. The results indicate that the complex is completely delocalized along the internal rotational coordinate. Ab initio calculations are also presented that are in good agreement with this picture. © 1995 American Institute of Physics.
    Type of Medium: Electronic Resource
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