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1.
Invertebr Syst ; 382024 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-38744500

RESUMEN

The integration of morphological and molecular lines of evidence has enabled the family Deltocyathidae to be erected to accommodate Deltocyathus species that were previously ascribed to the family Caryophylliidae. However, although displaying the same morphological characteristics as other species of Deltocyathus , molecular data suggested that D. magnificus was phylogenetically distant from Deltocyathidae, falling within the family Turbinoliidae instead. To elucidate the enigmatic evolutionary history of this species and skeletal microstructural features, the phylogenetic relationships of Deltocyathidae and Turbinoliidae were investigated using nuclear ultraconserved and exon loci and complete mitochondrial genomes. Both nuclear and mitochondrial phylogenomic reconstructions confirmed the position of D. magnificus within turbinolids. Furthermore, a novel mitochondrial gene order was uncovered for Deltocyathidae species. This gene order was not present in Turbinoliidae or in D. magnificus that both have the scleractinian canonical gene order, further indicating the taxonomic utility of mitochondrial gene order. D. magnificus is therefore formally moved to the family Turbinoliidae and accommodated in a new genus (Dennantotrochus Kitahara, Vaga & Stolarski, gen. nov.). Surprisingly, turbinolids and deltocyathids do not differ in microstructural organisation of the skeleton that consists of densely packed, individualised rapid accretion deposits and thickening deposits composed of fibres perpendicular to the skeleton surface. Therefore, although both families are clearly evolutionarily divergent, macromorphological features indicate a case of skeletal convergence while these may still share conservative biomineralisation mechanisms. ZooBank: urn:lsid:zoobank.org:pub:5F1C0E25-3CC6-4D1F-B1F0-CD9D0014678E.


Asunto(s)
Antozoos , Filogenia , Animales , Antozoos/genética , Antozoos/clasificación , Genoma Mitocondrial/genética , Evolución Biológica
2.
Mol Phylogenet Evol ; 175: 107565, 2022 10.
Artículo en Inglés | MEDLINE | ID: mdl-35787457

RESUMEN

Molecularly, the family Caryophylliidae is polyphyletic and different sets of genetic data converge towards a consensus that a taxonomic review of this family is necessary. Overall, the order of genes in the mitochondrial genome (mitogenome) together with DNA sequences have been used to successfully untangle evolutionary relationships in several groups of organisms. Published mitogenomes of two caryophylliid genera (Desmophyllum and Solenosmilia) present a transposition of the gene block containing cob, nad2, and nad6, which is located between nad5 5' exon and trnW, while that of Polycyathus chaishanensis presents the same gene order as the majority of scleractinian corals. In molecular-based evolutionary reconstructions, caryophylliids that have the mitochondrial gene rearrangement were recovered as a monophyletic lineage ("true" caryophylliids), while members of the genus Polycyathus were placed in a different position. In this study, additional mitogenomes of this family were assembled and included in evolutionary reconstructions of Scleractinia in order to improve our understanding on whether the mitogenome gene rearrangement is limited to and, therefore, could be a synapomorphy of the actual members of Caryophylliidae. Specimens of Caryophyllia scobinosa, Premocyathus sp., Heterocyathus sulcatus, and Trochocyathus caryophylloides, as well as Desmophyllum pertusum and Solenosmilia variabilis from the Southwest Atlantic were sequenced using Illumina platforms. Then, mitochondrial genomes were assembled and annotated, and nuclear datasets were recovered in-silico from assembled contigs using a previously published set of baits. Evolutionary reconstructions were performed using mitochondrial and nuclear datasets and based on Maximum Likelihood and Bayesian Inference. Obtained mitogenomes are circular and range between 15,816 and 18,225 bp in size and from 30.76% to 36.63% in GC content. The gene rearrangement is only seen in C. scobinosa, D. pertusum, Premocyathus sp., and S. variabilis, which were recovered as a monophyletic clade in both mitochondrial and nuclear phylogenies. On the other hand, the "caryophylliids" with the canonical mitogenome gene order were not recovered within this clade. Differences in features of the skeleton of "true" caryophylliids in comparison to traditional members of the family were observed and offer further support that the gene rearrangement might be seen as a synapomorphy of family Caryophylliidae.


Asunto(s)
Antozoos , Genoma Mitocondrial , Animales , Antozoos/genética , Teorema de Bayes , Orden Génico , Genes Mitocondriales , Filogenia
4.
J Struct Biol ; 185(1): 79-88, 2014 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-24511631

RESUMEN

Using in situ (12 h) pulse-labeling of scleractinian coral aragonitic skeleton with stable 86Sr isotope, the diel pattern of skeletal extension was investigated in the massive Porites lobata species, grown at 5 m depth in the Gulf of Eilat. Several microstructural aspects of coral biomineralization were elucidated, among which the most significant is simultaneous extension of the two basic microstructural components Rapid Accretion Deposits (RAD; also called Centers of Calcification) and Thickening Deposits (TD; also called fibers), both at night and during daytime. Increased thickness of the 86Sr-labeled growth-front in the RADs compared to the adjacent TDs revealed that in this species RADs extend on average twice as fast as TDs. At the level of the individual corallite, skeletal extension is spatially highly heterogeneous, with sporadic slowing or cessation depending on growth directions and skeletal structure morphology. Daytime photosynthesis by symbiotic dinoflagellates is widely acknowledged to substantially increase calcification rates at the colony and the corallite level in reef-building corals. However, in our study, the average night-time extension rate (visualized in three successive 12 h pulses) was similar to the average daytime extension (visualized in the initial 12 h pulse), in all growth directions and skeletal structures. This research provides a platform for further investigations into the temporal calibration of coral skeletal extension via cyclic growth increment deposition, which is a hallmark of coral biomineralization.


Asunto(s)
Antozoos/crecimiento & desarrollo , Antozoos/fisiología , Calcificación Fisiológica/fisiología , Isótopos de Estroncio/metabolismo , Animales , Antozoos/metabolismo , Fotosíntesis/fisiología , Esqueleto
5.
Geobiology ; 11(1): 29-43, 2013 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-23121244

RESUMEN

This paper reports the results of micro- to nanostructural and geochemical analyses of calcitic skeletons from extant deep-sea stalked crinoids. Fine-scale (SEM, FESEM, AFM) observations show that the crinoid skeleton is composed of carbonate nanograins, about 20-100 nm in diameter, which are partly separated by what appears to be a few nm thick organic layers. Sub-micrometre-scale geochemical mapping of crinoid ossicles using a NanoSIMS ion microprobe, combined with synchrotron high-spatial-resolution X-ray micro-fluorescence (µ-XRF) maps and X-ray absorption near-edge structure spectroscopy (XANES) show that high Mg concentration in the central region of the stereom bars correlates with the distribution of S-sulphate, which is often associated with sulphated polysaccharides in biocarbonates. These data are consistent with biomineralization models suggesting a close association between organic components (including sulphated polysaccharides) and Mg ions. Additionally, geochemical analyses (NanoSIMS, energy dispersive spectroscopy) reveal that significant variations in Mg occur at many levels: within a single stereom trabecula, within a single ossicle and within a skeleton of a single animal. Together, these data suggest that physiological factors play an important role in controlling Mg content in crinoid skeletons and that great care should be taken when using their skeletons to reconstruct, for example, palaeotemperatures and Mg/Ca palaeo-variations of the ocean.


Asunto(s)
Equinodermos/química , Equinodermos/ultraestructura , Geología/métodos , Paleontología/métodos , Agua de Mar/química , Animales , Bahamas , Calcio/análisis , Calcio/química , Calcio/metabolismo , Equinodermos/metabolismo , Japón , Magnesio/análisis , Magnesio/química , Magnesio/metabolismo , Temperatura
6.
Gen Comp Endocrinol ; 104(2): 197-202, 1996 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-8930610

RESUMEN

The plasma levels of arginine vasotocin (AVT) and isotocin (IT) in rainbow trout (Oncorhynchus mykiss) were studied to assess possible diurnal variations in neurohypophysial nonapeptides. Fish were kept under natural photoperiod and adapted to fresh and brackish Baltic water. Blood was sampled at 5:00, 11:00, 16:00, 22:30, and again at 5:00. Hormones were determined by gradient high-performance liquid chromatography preceded by solid-phase extraction. The marked diurnal changes of AVT were detected in plasma of fish adapted to both fresh and brackish waters. AVT levels (fmol/ml) were maximal at 16:00 and minimal at 5:00 (253.4 +/- 35.7 and 45.5 +/- 17.3, respectively). Unlike AVT, isotocin levels displayed no diurnal changes. AVT concentrations at 11:00, 16:00, and 22:30 were significantly higher than IT values measured throughout the day. Plasma AVT concentrations determined in brackish water-adapted fish at 16:00 were significantly lower than those of freshwater-adapted fish at the same time. These data suggest that synthesis and/or release of AVT and IT are controlled independently, so that these nonapeptides have different physiological roles in teleost fish. AVT might participate in circadian time-keeping system in fish.


Asunto(s)
Adaptación Fisiológica/fisiología , Ritmo Circadiano/fisiología , Oncorhynchus mykiss/fisiología , Oxitocina/análogos & derivados , Vasotocina/sangre , Animales , Femenino , Agua Dulce , Masculino , Oncorhynchus mykiss/sangre , Oxitocina/sangre , Oxitocina/metabolismo , Agua de Mar , Vasotocina/metabolismo
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