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  • Kamanli, Seyit A.  (2)
  • 1
    Online Resource
    Online Resource
    Cambridge University Press (CUP) ; 2016
    In:  The Paleontological Society Papers Vol. 22 ( 2016-09), p. 39-55
    In: The Paleontological Society Papers, Cambridge University Press (CUP), Vol. 22 ( 2016-09), p. 39-55
    Abstract: Confocal laser scanning microscopy is a well-established optical technique allowing for three-dimensional (3-D) visualization of fluorescent specimens with a resolution close to the diffraction limit of light. Thanks to the availability of a wide range of fluorescent dyes and selective staining using antibodies, the technique is commonly used in life sciences as a powerful tool for studying different biological processes, often at the level of single molecules. However, this type of approach is often not applicable for specimens that are preserved in historical slide collections, embedded in amber, or are fossilized, and cannot be exposed to any form of selective staining or other form of destructive treatment. This usually narrows the number of microscopic techniques that can be used to study such specimens to traditional light microscopy or scanning electron microscopy. However, these techniques have their own limitations and cannot fully reveal 3-D structures within such barely accessible samples. Can confocal microscopy be of any help? The answer is positive, and it is due to the fact that many paleontological specimens exhibit a strong inherent autofluorescence that can serve as an excellent source of emitted photons for confocal microscopy visualizations either through reconstruction of the induced autoflourescent signal from the sample, or through reconstruction of the reflected signal from the sample surface. Here, we describe the workflow and methodology involved in acquiring confocal data from a sample and reprocessing the resulting image stack using the image-processing program imageJ before reconstructing the data using the open-source 3-D rendering program, Drishti. This approach opens new possibilities for using confocal microscopy in a nondestructive manner for visualizing complex paleontological material that has never previously been considered as suitable for this type of microscopic technique.
    Type of Medium: Online Resource
    ISSN: 1089-3326 , 2399-7575
    Language: English
    Publisher: Cambridge University Press (CUP)
    Publication Date: 2016
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  • 2
    In: Invertebrate Systematics, CSIRO Publishing, Vol. 31, No. 6 ( 2017), p. 797-
    Abstract: In his catalogue of British Museum Crustacea, Adam White listed two swimming crabs from Borneo as a new species, Amphitrite argentata, but he did not provide a description and therefore the name was a nomen nudum. Later, Alphonse Milne-Edwards described the larger of these male specimens as Neptunus argentatus and credited the species to White. Now assigned to Monomia Gistel, 1848, M. argentata was recently considered to represent a species-complex; however, its nomenclature and taxonomy have been confused over a long period of time. Furthermore, the larger syntype examined by Alphonse Milne-Edwards is no longer extant. The present study compared the smaller extant M. argentata male of White, here designated as the lectotype, with the description by A. Milne-Edwards. This dried specimen was re-examined using X-ray and computed tomography scanning techniques in order to reveal the general morphology of the first male gonopod (G1). Fresh material was collected and identified with confidence as M. argentata. This species was redescribed to modern standards including illustrations, details of coloration and new scanning electron micrographs of the G1 were provided. The validity of this species was further endorsed by comparing DNA sequences with congeners from the South China Sea. To conclude, the type status, authority and associated species-complex of M. argentata are discussed.
    Type of Medium: Online Resource
    ISSN: 1445-5226
    Language: English
    Publisher: CSIRO Publishing
    Publication Date: 2017
    SSG: 12
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