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Search Results (221)

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25 pages, 8944 KiB  
Article
Paleoenvironmental Reconstruction and Hydrocarbon Potential of the Westphalian-A Kozlu Formation Hard Coal in the Zonguldak Basin: Insights from Organic Geochemistry and Petrology
by Neslihan Ünal-Kartal and Selin Karadirek
Minerals 2024, 14(10), 971; https://doi.org/10.3390/min14100971 - 26 Sep 2024
Viewed by 374
Abstract
The Zonguldak coal basin is the area with the most important hard coal reserves in Turkey. This study focuses on coal samples extracted from three seams of the Kozlu Formation, specifically from the Kozlu underground mine, to assess the coals’ organic geochemical and [...] Read more.
The Zonguldak coal basin is the area with the most important hard coal reserves in Turkey. This study focuses on coal samples extracted from three seams of the Kozlu Formation, specifically from the Kozlu underground mine, to assess the coals’ organic geochemical and petrographic properties. Analytical methods, including TOC-pyrolysis, biomarker analysis, and maceral distribution studies, were employed. Based on these analyses, the paleoenvironmental conditions and hydrocarbon generation potential of the coals were evaluated. The results reveal that the coals, characterized by high TOC, high HI, and low OI, contain type II–III kerogen. These findings, coupled with the high QI and low BI values, suggest the presence of oil–gas prone source rocks. Elevated Tmax (457–466 °C) and Rr (0.89%–1.17%) values indicate a maturity level ranging from mature to overmature stages. High GI and GWI values suggest a significant degree of gelification and wet conditions during formation. The high Pr/Ph (1–6.58), C31R/C30 hopane (<0.25), and low DBT/P (0.27–0.50) ratios show that the Acılık seam was formed in a lacustrine environment under anoxic–suboxic conditions, whereas the Büyük and Domuzcu seams were formed in a fluvial/deltaic environment under oxic conditions. The findings of this study suggest that the paleovegetation in coal-forming environments consisted of aquatic and herbaceous plants. Full article
Show Figures

Figure 1

Figure 1
<p>Geological and location maps of the investigated area (modified from [<a href="#B18-minerals-14-00971" class="html-bibr">18</a>,<a href="#B29-minerals-14-00971" class="html-bibr">29</a>,<a href="#B37-minerals-14-00971" class="html-bibr">37</a>,<a href="#B41-minerals-14-00971" class="html-bibr">41</a>]).</p>
Full article ">Figure 2
<p>(<b>a</b>) Generalized stratigraphic section of the investigated area (modified from [<a href="#B18-minerals-14-00971" class="html-bibr">18</a>,<a href="#B22-minerals-14-00971" class="html-bibr">22</a>,<a href="#B41-minerals-14-00971" class="html-bibr">41</a>]). (<b>b</b>) The section of the Acılık, Domuzcu, and Büyük seams from the Kozlu Formation and location of samples (modified from [<a href="#B44-minerals-14-00971" class="html-bibr">44</a>]).</p>
Full article ">Figure 3
<p>n-Alkane and isoprenoid distribution of selected coal samples.</p>
Full article ">Figure 4
<p>(<b>a</b>) <span class="html-italic">m</span>/<span class="html-italic">z</span> 191 and (<b>b</b>) <span class="html-italic">m</span>/<span class="html-italic">z</span> 217 mass fragmentograms of the saturated hydrocarbon fraction in the selected coal samples.</p>
Full article ">Figure 5
<p>(<b>a</b>) <span class="html-italic">m</span>/<span class="html-italic">z</span> 231 mass fragmentograms, (<b>b</b>) <span class="html-italic">m</span>/<span class="html-italic">z</span> 253 mass fragmentograms, (<b>c</b>) <span class="html-italic">m</span>/<span class="html-italic">z</span> 178 + 192 mass fragmentograms, and (<b>d</b>) <span class="html-italic">m</span>/<span class="html-italic">z</span> 184 + 198 mass fragmentograms of aromatic hydrocarbons for selected coal samples.</p>
Full article ">Figure 6
<p>Representative microphotographs of the various macerals of coal samples from Kozlu Formation. Gelinite (G), Sporinite (Sp), Cutinite (Cut), Corpogelinite (Cg), Fusinite (F), Semifusinite (Sf), Vitrodetrinite (Vd), Resinite (R), Inertodetrinite (Id), and Macrinite (Mac).</p>
Full article ">Figure 7
<p>Pr/n-C<sub>17</sub> vs. Ph/n-C<sub>18</sub> diagram illustrating the organic matter source input for analyzed coal samples from the Kozlu Formation.</p>
Full article ">Figure 8
<p>C<sub>27</sub>-C<sub>28</sub>-C<sub>29</sub> sterane ternary diagram for coal samples from the Kozlu Formation.</p>
Full article ">Figure 9
<p>Cross plot of (<b>a</b>) HI versus Tmax, (<b>b</b>) HI-Ro, (<b>c</b>) BI-Tmax, and (<b>d</b>) QI-Tmax for analyzed coal samples.</p>
Full article ">Figure 10
<p>Relation between C<sub>31</sub>R/C<sub>30</sub> hopane and Pr/Ph ratios for the analyzed samples.</p>
Full article ">Figure 11
<p>Coal facies diagrams for the analyzed coal samples. (<b>a</b>) TPI-GI (modified from [<a href="#B53-minerals-14-00971" class="html-bibr">53</a>]) (<b>b</b>) VI-GWI (modified from [<a href="#B52-minerals-14-00971" class="html-bibr">52</a>]).</p>
Full article ">Figure 12
<p>DBT versus Pr/Ph for the analyzed coal samples.</p>
Full article ">Figure 13
<p>Cross-plot of TOC versus Rock-Eval S2 for the analyzed samples.</p>
Full article ">
33 pages, 49504 KiB  
Article
The Late Early–Middle Pleistocene Mammal Fauna from the Megalopolis Basin (Peloponnese, Greece) and Its Importance for Biostratigraphy and Paleoenvironment
by George E. Konidaris, Athanassios Athanassiou, Vangelis Tourloukis, Krystalia Chitoglou, Thijs van Kolfschoten, Domenico Giusti, Nicholas Thompson, Georgia Tsartsidou, Effrosyni Roditi, Eleni Panagopoulou, Panagiotis Karkanas and Katerina Harvati
Quaternary 2024, 7(4), 41; https://doi.org/10.3390/quat7040041 - 24 Sep 2024
Viewed by 1659
Abstract
Recent investigations in the upper Lower–Middle Pleistocene deposits of the Megalopolis Basin (Greece) led to the discovery of several sites/findspots with abundant faunal material. Here, we provide an updated overview including new results on the micro- and macro-mammal fauna. Important new discoveries comprise [...] Read more.
Recent investigations in the upper Lower–Middle Pleistocene deposits of the Megalopolis Basin (Greece) led to the discovery of several sites/findspots with abundant faunal material. Here, we provide an updated overview including new results on the micro- and macro-mammal fauna. Important new discoveries comprise partial hippopotamus skeletons from Marathousa 1 and the new Lower Pleistocene site Choremi 6, as well as a second partial elephant skeleton from Marathousa 1, including a complete tusk and the rarely found stylohyoideum. Based on the first results from the newly collected micromammals, we discuss age constraints of the sites, and we provide biostratigraphic/biochronologic remarks on key mammal taxa for the Middle Pleistocene of Greece and southeastern Europe. The presence of mammals highly dependent on freshwater for their survival, together with temperate-adapted ones in several stratigraphic layers of the basin, including those correlated with glacial stages, when conditions were colder and/or drier, indicate the capacity of the basin to retain perennial freshwater bodies under milder climatic conditions, even during the harsher glacial periods of the European Middle Pleistocene, and further support its refugial status. Yet, the smaller dimensions of the Megalopolis hippopotamuses may represent a response to the changing environmental conditions of the epoch, not optimal for hippopotamuses. Overall, the Megalopolis Basin comprises a unique fossil record for southeastern Europe and provides valuable insights into the Middle Pleistocene terrestrial ecosystems of Europe, and hominin adaptations in particular. Full article
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Figure 1

Figure 1
<p>(<b>a</b>) Geographic position of the Megalopolis Basin (maps taken from Copernicus Land Monitoring Service: <a href="https://land.copernicus.eu/" target="_blank">https://land.copernicus.eu/</a> and <a href="https://maps-for-free.com/" target="_blank">https://maps-for-free.com/</a> (accessed on 30 April 2024)). (<b>b</b>) Geographic position of the investigated sites within the lignite mines (numbered 1–4) of the Megalopolis Basin (satellite image from Google Earth). (<b>c</b>) Panoramic view of the eastern quarry of the Marathousa mine, indicating the Marathousa and Megalopolis Members of the Choremi Formation, and the lignite seams. (<b>d</b>) Simplified stratigraphic column of the Marathousa Member showing the lignite seams and the intercalating detrital intervals, their correlation to the Marine Isotope Stages (MIS) following the age model proposed by Tourloukis et al. [<a href="#B3-quaternary-07-00041" class="html-bibr">3</a>], and the stratigraphic position of the sites and survey units following Karkanas et al. [<a href="#B25-quaternary-07-00041" class="html-bibr">25</a>,<a href="#B28-quaternary-07-00041" class="html-bibr">28</a>].</p>
Full article ">Figure 2
<p>(<b>a</b>) Panoramic view of the site Choremi 6. (<b>b</b>–<b>e</b>) Fossils belonging to the <span class="html-italic">Hippopotamus antiquus</span> skeleton in situ at Choremi 6. (<b>f</b>) Distribution map showing the position of the hippopotamus remains (recorded with the use of a Differential GPS—WGS84 datum).</p>
Full article ">Figure 3
<p><span class="html-italic">Hippopotamus antiquus</span> remains from Choremi 6. (<b>a</b>) Lower molar (m1?) in occlusal view; (<b>b</b>) series of caudal vertebrae (CHO-6-36, 37, 38, 39, 40, and 41); (<b>c</b>,<b>d</b>) left scapula (CHO-6-49) in lateral (<b>c</b>) and distal (<b>d</b>) view; (<b>e</b>) right patella (CHO-6-10) in caudal view; (<b>f</b>) left tibia (CHO-6-42) in dorsal view (note the presence of a limonite concretion on the distal end); (<b>g</b>) left fibula (CHO-6-43) in medial view; (<b>h</b>) left astragalus (CHO-6-7) in dorsal view; (<b>i</b>) left navicular (central tarsal, CHO-6-15) in lateral view; (<b>j</b>) left calcaneus (CHO-6-8) in medial view; (<b>k</b>) left ectocuneiform (tarsal I, CHO-6-17) in proximal view; (<b>l</b>) left mesocuneiform (tarsal II, CHO-6-25) in proximal view; (<b>m</b>) left entocuneiform (tarsal III, CHO-6-11) in distal view; (<b>n</b>) left cuboid (tarsal IV, CHO-6-13) in medial view; (<b>o</b>) left Mt II (CHO-6-20) in dorsal view; (<b>p</b>) left MT V (CHO-6-24) in dorsal view; (<b>q</b>) right MT III (CHO-6-21) in dorsal view.</p>
Full article ">Figure 4
<p>Metrical comparison of <span class="html-italic">Hippopotamus</span> postcranial specimens from Megalopolis Basin with <span class="html-italic">Hippopotamus antiquus</span>, <span class="html-italic">Hippopotamus tiberinus</span> (<span class="html-italic">H</span>. ex gr. <span class="html-italic">antiquus</span>), and <span class="html-italic">Hippopotamus amphibius</span>. Data from [<a href="#B12-quaternary-07-00041" class="html-bibr">12</a>,<a href="#B20-quaternary-07-00041" class="html-bibr">20</a>,<a href="#B33-quaternary-07-00041" class="html-bibr">33</a>,<a href="#B34-quaternary-07-00041" class="html-bibr">34</a>,<a href="#B35-quaternary-07-00041" class="html-bibr">35</a>,<a href="#B36-quaternary-07-00041" class="html-bibr">36</a>,<a href="#B37-quaternary-07-00041" class="html-bibr">37</a>]. The blue and green lines correspond to the ranges of <span class="html-italic">H. amphibius</span> and <span class="html-italic">H. antiquus</span> given by [<a href="#B38-quaternary-07-00041" class="html-bibr">38</a>]. Abbreviations: a, articular facet; d, distal; DAP, anteroposterior diameter; DT, transverse diameter; H, height; L, length; med, medial; p, proximal.</p>
Full article ">Figure 5
<p>Small mammals from several sites and findspots of the Megalopolis Basin. (<b>a</b>,<b>b</b>) Right M2 (KYP-4-MM008) of <span class="html-italic">Mimomys</span> sp. (smaller size) from Kyparissia 4 in occlusal (<b>a</b>) and lingual (<b>b</b>) view; (<b>c</b>,<b>d</b>) left m1 (KYP-4-MM017) of <span class="html-italic">Mimomys</span> cf. <span class="html-italic">savini</span> from Kyparissia 4 in occlusal (<b>c</b>) and lingual (<b>d</b>) view; (<b>e</b>,<b>f</b>) left M3 (KYP-4-MM015) of <span class="html-italic">Pliomys</span> sp. from Kyparissia 4 in occlusal (<b>e</b>) and lingual (<b>f</b>) view; (<b>g</b>,<b>h</b>) left m2 (KYP-3-MM001) of <span class="html-italic">Mimomys</span> sp. (smaller size) from Kyparissia 3 in occlusal (<b>g</b>) and lingual (<b>h</b>) view; (<b>i</b>) right m1 (KYP SU 6-MM002) of <span class="html-italic">Pliomys</span> cf. <span class="html-italic">episcopalis</span> from Kyparrisia SU 6 in occlusal view; (<b>j</b>,<b>k</b>) left m1 (CHO-7-MM135) of <span class="html-italic">Arvicola mosbachensis</span> from Choremi 7 in occlusal (<b>j</b>) and lingual (<b>k</b>) view; (<b>l</b>) left m1 (CHO-7-MM66) of <span class="html-italic">Microtus</span> sp. (cf. <span class="html-italic">Microtus arvalis</span>) from Choremi 7 in occlusal view; (<b>m</b>) right m1 (CHO-7-MM214) of <span class="html-italic">Microtus</span> (<span class="html-italic">Terricola</span>) <span class="html-italic">subterraneus</span> from Choremi 7 in occlusal view.</p>
Full article ">Figure 6
<p>(<b>a</b>) Panoramic view of the Choremi 4 section showing the fossiliferous layer. (<b>b</b>) A tooth of <span class="html-italic">Castor fiber</span> in situ within a shell-rich layer. (<b>c</b>) In situ concentration of hippopotamus bones. (<b>d</b>,<b>e</b>) Right astragalus of <span class="html-italic">Hippopotamus antiquus</span> in dorsal (<b>d</b>) and plantar (<b>e</b>) view. (<b>f</b>) Right entocuneiform (tarsal III) in proximal view. (<b>g</b>,<b>h</b>) Atlas of <span class="html-italic">H. antiquus</span> in cranial (<b>g</b>) and caudal (<b>h</b>) view. (<b>i</b>–<b>l</b>) Right astragalus of <span class="html-italic">Bison</span> sp. found at the surface near the Choremi 4 section in dorsal (<b>i</b>), plantar (<b>j</b>), medial (<b>k</b>), and lateral (<b>l</b>) view.</p>
Full article ">Figure 7
<p>(<b>a</b>) Panoramic view of the northern profile in the Marathousa mine, indicating the Marathousa and Megalopolis Members, the lignite seams, and the location of the MAR SU 7. (<b>b</b>) Details of the profile showing the MAR SU 7 section. (<b>c</b>,<b>d</b>) Left calcaneus of <span class="html-italic">Castor fiber</span> in medial (<b>c</b>) and plantar (<b>d</b>) view. (<b>e</b>–<b>h</b>) Left humerus of <span class="html-italic">Lutra simplicidens</span> in cranial (<b>e</b>), caudal (<b>f</b>), medial (<b>g</b>), and lateral (<b>h</b>) view. (<b>i</b>,<b>j</b>) Left radius of a <span class="html-italic">Capreolus</span>-sized cervid in dorsal (<b>i</b>) and volar (<b>j</b>) view. (<b>k</b>,<b>l</b>) Metacarpal of a <span class="html-italic">Capreolus</span>-sized cervid in dorsal (<b>k</b>) and volar (<b>l</b>) view.</p>
Full article ">Figure 8
<p><span class="html-italic">Hippopotamus antiquus</span> skeleton from Marathousa 1 (Area B; UB2b). (<b>a</b>) Distribution map showing the position (recorded with the use of a total station) of the hippopotamus remains; (<b>b</b>) hippopotamus fossils in situ; (<b>c</b>) sacrum (MAR-1B-926/587-17) in ventral view; (<b>d</b>) right radius (MAR-1B-1) in dorsal view; (<b>e</b>) right patella (MAR-1B-925/587-2) in caudal view; (<b>f</b>) right femur (MAR-1B-925/587-1) in cranial view; (<b>g</b>) right tibia (MAR-1B-926/587-10) in dorsal view; (<b>h</b>) right astragalus (MAR-1B-926/587-4) in dorsal view; (<b>i</b>) right calcaneus (MAR-1B-2) in medial view; (<b>j</b>) right navicular (central tarsal, MAR-1B-924/587-3) in lateral view; (<b>k</b>) right MT II (MAR-1B-4) in dorsal view; (<b>l</b>) right MT V (MAR-1B-926/586-1) in dorsal view; (<b>m</b>) lumbar vertebra (MAR-1B-926/587-9) in cranial view.</p>
Full article ">Figure 9
<p>(<b>a</b>,<b>b</b>) Left m2 (MAR-1B-8) of <span class="html-italic">Hippopotamus antiquus</span> from Marathousa 1 (Area B), most possibly belonging to the hippopotamus skeleton, in occlusal (<b>a</b>) and buccal (<b>b</b>) view. (<b>c</b>) Biplot comparing <span class="html-italic">Hippopotamus</span> m2 from various localities. (<b>d</b>,<b>e</b>) Left M3 (MAR-1B-7) of <span class="html-italic">H. antiquus</span> from Marathousa 1 (Area B), most possibly belonging to the hippopotamus skeleton, in occlusal (<b>d</b>) and buccal (<b>e</b>) view. (<b>f</b>) Biplot comparing <span class="html-italic">Hippopotamus</span> M3 from various localities. (<b>g</b>) Left M2 of <span class="html-italic">H. antiquus</span> from MAR SU 1 in occlusal view. (<b>h</b>) Left M2 of <span class="html-italic">H. antiquus</span> from MAR SU 2 in occlusal view. (<b>i</b>) Biplot comparing <span class="html-italic">Hippopotamus</span> M2 from various localities. Biplots with 95% confidence ellipses for <span class="html-italic">Hippopotamus amphibius</span> and <span class="html-italic">H. antiquus</span>, performed with the software package PAST v. 4.16 [<a href="#B63-quaternary-07-00041" class="html-bibr">63</a>]. Data are from [<a href="#B33-quaternary-07-00041" class="html-bibr">33</a>,<a href="#B64-quaternary-07-00041" class="html-bibr">64</a>,<a href="#B65-quaternary-07-00041" class="html-bibr">65</a>,<a href="#B66-quaternary-07-00041" class="html-bibr">66</a>,<a href="#B67-quaternary-07-00041" class="html-bibr">67</a>,<a href="#B68-quaternary-07-00041" class="html-bibr">68</a>].</p>
Full article ">Figure 10
<p><span class="html-italic">Palaeoloxodon antiquus</span> skeleton from Marathousa 1 (Area B; UB4c). (<b>a</b>) Tusk and cervical vertebrae (including the axis) in situ. (<b>b</b>) Distribution map of the southwestern part of the trench at Area B showing the position (recorded with the use of a total station) of the elephant remains, stratigraphically and spatially associated with lithic artefacts and other faunal remains. (<b>c</b>,<b>d</b>) Axis (MAR-1B-928/588-39) in cranial (<b>c</b>) and right lateral (<b>d</b>) view; (<b>e</b>) cervical vertebra (MAR-1B-928/586-16) in cranial view; (<b>f</b>–<b>h</b>) left stylohyoid (MAR-1B-928/587-32) in medial (<b>f</b>), lateral (<b>g</b>), and anterior (<b>h</b>) view.</p>
Full article ">Figure 11
<p>Mammal remains from Marathousa 1. (<b>a</b>,<b>b</b>) Left hemimandible with the incisor and p4–m3 of <span class="html-italic">Castor fiber</span> (surface find at Area B) in medial (<b>a</b>) and dorsal (<b>b</b>) view. (<b>c</b>) Left hemimandible (MAR-1A-941/677-41) of <span class="html-italic">Castor fiber</span> in situ at Area A. (<b>d</b>,<b>e</b>) Second phalanx of the front limb (MAR-1B-930/593-46) of <span class="html-italic">Bison</span> sp. in dorsal (<b>d</b>) and lateral (<b>e</b>) view. (<b>f</b>,<b>g</b>) Third phalanx of the front limb (MAR-1B-931/594-42) of <span class="html-italic">Bison</span> sp. in lateral (<b>f</b>) and medial (<b>g</b>) view. (<b>h</b>) Refitting mandibular fragments (MAR-1B-934/594-71, 932/598-51, 933/595-60, 931/593-38, and 931/596-39) of the same individual of <span class="html-italic">Dama</span> sp., above the right hemimandible in medial view, and below the left hemimandible in lateral view. (<b>i</b>,<b>j</b>) Left scapula fragment (MAR-1B-934/597-35) of <span class="html-italic">Dama</span> sp. in lateral (<b>i</b>) and distal (<b>j</b>) view. (<b>k</b>) Left calcaneus (MAR-1B-928/588-21) of <span class="html-italic">Dama</span> sp. in plantar view. (<b>l</b>,<b>m</b>) Left scapula fragment (MAR-1A-935/672-20) of <span class="html-italic">Cervus elaphus</span> in lateral (<b>l</b>) and distal (<b>m</b>) view. (<b>n</b>) Distal fragment of left humerus (MAR-1B-931/564-58) of <span class="html-italic">C. elaphus</span> in cranial view. (<b>o</b>) Proximal fragment of left radius (MAR-1B-926-587-22) in dorsal view. (<b>p</b>) Distal fragment of left tibia (MAR-1B-925/586-7) in dorsal view. (<b>q</b>) Right astragalus (MAR-1B-926/586-4) of <span class="html-italic">C. elaphus</span> in dorsal view. (<b>r</b>) Left calcaneus (MAR-1-939/635-1) of <span class="html-italic">C. elaphus</span> in medial view. (<b>s</b>) Left MT IV (MAR-1A-941/672-44) of <span class="html-italic">Canis</span> sp. in dorsal view. Silhouette images from PhyloPic, phylopic.org.</p>
Full article ">Figure 12
<p>Mammal remains from Tripotamos 4 (TRP-4) and Choremi 7 (CHO-7). (<b>a</b>) Antler fragment (TRP-4-F2) of <span class="html-italic">Cervus elaphus</span> in lateral view; (<b>b</b>) distal metacarpal (TRP-4-F57) of <span class="html-italic">Dama</span> sp. in dorsal view; (<b>c</b>) distal metacarpal (TRP-4-F47) of <span class="html-italic">Dama</span> sp. in dorsal view; (<b>d</b>–<b>f</b>) lower molar (TRP-4-F2, surface) of Bovini in lingual (<b>d</b>), occlusal (<b>e</b>), and buccal (<b>f</b>) view; (<b>g</b>) fragment of upper canine (TRP-4-F70) of <span class="html-italic">Hippopotamus</span> sp.; (<b>h</b>) lamellar fragment (TRP-4-F36, F44, F58, and F73) of Elephantidae indet.; (<b>i</b>–<b>k</b>) right hemimandible fragment with m1–m3 (CHO-7-F125) of <span class="html-italic">Cervus elaphus</span> in lateral (<b>i</b>), lingual (<b>j</b>), and occlusal (<b>k</b>) view; (<b>l</b>–<b>n</b>) right m3 (CHO-7-F147) of <span class="html-italic">Bos</span> sp. in occlusal (<b>l</b>), lingual (<b>m</b>), and buccal (<b>n</b>); (<b>o</b>–<b>q</b>) upper molar (CHO-7-F68) of <span class="html-italic">Bos</span> sp. in occlusal (<b>o</b>), buccal (<b>p</b>), and lingual (<b>q</b>) view.</p>
Full article ">Figure 13
<p>(<b>a</b>,<b>b</b>) Tusk fragment of <span class="html-italic">Palaeoloxodon antiquus</span> from CHO SU 11 in cross-sectional (<b>a</b>) and lateral (<b>b</b>) view. (<b>c</b>–<b>e</b>) Left upper molar of cf. <span class="html-italic">Bos</span> from Choremi 5 in occlusal (<b>c</b>), lingual (<b>d</b>), and buccal (<b>e</b>) view. (<b>f</b>) Distal metacarpal of <span class="html-italic">Bos</span> sp. from CHO SU 11 in dorsal view. (<b>g</b>,<b>h</b>) Right upper premolar (P3/P4) of <span class="html-italic">Equus</span> sp. from CHO SU 10, close to the site Choremi 6, in lingual (<b>g</b>) and occlusal (<b>h</b>) view. (<b>i</b>) Left astragalus of <span class="html-italic">Equus</span> sp. from MAR SU North in dorsal view. (<b>j</b>) Left astragalus of <span class="html-italic">Equus</span> sp. from CHO SU 7 in dorsal view. (<b>k</b>) Left radius and ulna of <span class="html-italic">Hippopotamus antiquus</span> from the Marathousa mine in lateral view.</p>
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<p>Simplified stratigraphic column of the Marathousa Member showing the lignite seams and the intercalating detrital intervals, their correlation to the Marine Isotope Stages (MIS) following the age model proposed by Tourloukis et al. [<a href="#B3-quaternary-07-00041" class="html-bibr">3</a>], the stratigraphic position of the sites and survey units following Karkanas et al. [<a href="#B25-quaternary-07-00041" class="html-bibr">25</a>,<a href="#B28-quaternary-07-00041" class="html-bibr">28</a>], and the biostratigraphic range of selected micro- and macro-mammals from the Megalopolis Basin, indicating their First and Last Occurrences in the Greek fossil record. Silhouette images from PhyloPic, phylopic.org.</p>
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14 pages, 3190 KiB  
Article
Geochemical Indicators on the Central Tibetan Plateau Lake Sediments: Historical Climate Change and Regional Sustainability
by Xi Ma, Xiaodan Wang, Yunlong Gao, Fujun Yue and Wei Chen
Sustainability 2024, 16(18), 8186; https://doi.org/10.3390/su16188186 - 20 Sep 2024
Viewed by 709
Abstract
This study investigates geochemical indicators (TOC, TN, C/N, δ13Corg, δ15N, and pollen indicators) from sediment samples of Zigetang Co Lake on the Tibetan Plateau (TP) to explore past climate changes in the lake basin. The findings aim to provide [...] Read more.
This study investigates geochemical indicators (TOC, TN, C/N, δ13Corg, δ15N, and pollen indicators) from sediment samples of Zigetang Co Lake on the Tibetan Plateau (TP) to explore past climate changes in the lake basin. The findings aim to provide essential data for developing sustainable strategies for the TP region. From 14.0 to 10.8 cal. ka BP, the δ15N, TOC, TN, and δ13Corg value of the lake sediments was relatively low; this indicated a low organic matter input into the lake, reflecting a probably cold and arid environment. In addition, the pollen was primarily composed of Artemisia and Gramineae, which are adapted to cold environments, further confirming that the climate during this period was likely cold and dry. From 10.8 to 8.2 cal. ka BP, the changes in the main plant composition were likely due to increased solar radiation, the onset of the monsoon, and higher temperatures and precipitation, which created more favorable conditions for the growth of Cyperaceae. From 8.2 to 4.2 cal. ka BP, when the solar radiation weakened and the monsoon diminished, the basin maintained relatively high water levels, with regional precipitation being likely influenced by westerly winds. From 4.2 to 0.01 cal. ka BP, δ13Corg and δ15N initially decreased and then increased, which was likely a transition from a cold–wet climate to warm–dry conditions during the late Holocene, and the Pollen sum also showed significant changes. Understanding climate evolution and vegetation changes is crucial for formulating timely policies to ensure regional sustainable development. Full article
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<p>(<b>a</b>) Geographical location of Zigetang Co Lake (the red star). (<b>b</b>) Geomorphic profile [<a href="#B32-sustainability-16-08186" class="html-bibr">32</a>] and coring site of Zigetang Co Lake (the red star).</p>
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<p>The variations in total organic carbon (TOC), total nitrogen (TN), and nitrogen isotopes (δ<sup>15</sup>N) with depth. The linear lines represent the linear fittings for their co-variations.</p>
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<p>The variations in TN, TOC, carbon/nitrogen ratio (C/N), organic carbon isotopes (δ<sup>13</sup>Corg), and δ<sup>15</sup>N in sediments. Each region of the chart represents the various climatic conditions in different late glacial periods.</p>
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<p>The correlations of TN with TOC (<b>a</b>) and δ<sup>15</sup>N (<b>b</b>) in the lake sediment.</p>
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<p>The variation in <span class="html-italic">Artemisia</span> and <span class="html-italic">Cyperaceae</span> pollen in Zigetang Co lake sediments.</p>
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<p>Source indications of sediment organic matter in Zigetang Co. The ranges of C<sub>3</sub>, C<sub>4</sub>, aquatic, and terrestrial plants were derived from previous studies [<a href="#B11-sustainability-16-08186" class="html-bibr">11</a>,<a href="#B43-sustainability-16-08186" class="html-bibr">43</a>,<a href="#B44-sustainability-16-08186" class="html-bibr">44</a>].</p>
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<p>Changes in the (<b>a</b>) TOC, (<b>b</b>) TN, (<b>c</b>) δ<sup>15</sup>N, and (<b>d</b>) δ<sup>13</sup>Corg over time, (<b>e</b>) the effective moisture in monsoonal Central Asia [<a href="#B56-sustainability-16-08186" class="html-bibr">56</a>] and the solar insolation at 32° N in June [<a href="#B53-sustainability-16-08186" class="html-bibr">53</a>]. OD and YD refer to the Older Dryas and the Younger Dryas, respectively. The yellow area indicates monsoon-influenced precipitation in the region, while the blue area indicates precipitation influenced by westerlies. The gray dashed lines delineate the areas corresponding to stages I, II, III, and IV.</p>
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30 pages, 19679 KiB  
Article
Paleoenvironmental Transition during the Rhuddanian–Aeronian and Its Implications for Lithofacies Evolution and Shale Gas Exploration: Insights from the Changning Area, Southern Sichuan Basin, South-West China
by Hangyi Zhu
Minerals 2024, 14(9), 949; https://doi.org/10.3390/min14090949 - 18 Sep 2024
Viewed by 443
Abstract
During the Rhuddanian–Aeronian interglacial period, global geological events such as glacial melting, synsedimentary volcanic activity, biological resurgence, and large-scale marine transgressions caused frequent fluctuations in paleoproductivity, climate changes, and sea level variations. These paleoenvironmental transitions directly influenced the development characteristics of shale lithofacies. [...] Read more.
During the Rhuddanian–Aeronian interglacial period, global geological events such as glacial melting, synsedimentary volcanic activity, biological resurgence, and large-scale marine transgressions caused frequent fluctuations in paleoproductivity, climate changes, and sea level variations. These paleoenvironmental transitions directly influenced the development characteristics of shale lithofacies. This study investigates the Longmaxi Formation shale in the Changning area in the Southern Sichuan basin, focusing on 28 core samples from Well N1. Using scanning electron microscopy, QEMSCAN, TOC, XRD, and major and trace element analyses, we reconstructed the paleoenvironmental transitions of this period and explored their control over shale lithofacies types and mineral compositions. Four shale lithofacies were identified: carbonate rich lithofacies (CRF), biogenic quartz-rich lithofacies (BQRF), detrital clay-rich lithofacies (CRDF), and detrital quartz-rich lithofacies (DQRF). During the Rhuddanian period, rising global temperatures caused glacial melting and rapid marine transgressions. The low oxygen levels in bottom waters, combined with upwelling and abundant volcanic material, led to high paleoproductivity. This period primarily developed BQRF and CRF. Rich nutrients and abundant siliceous organisms, along with anoxic to anaerobic conditions, provided the material basis and preservation conditions for high biogenic quartz and organic matter content. High paleoproductivity and anoxic conditions also facilitated the precipitation of synsedimentary calcite and supplied Mg2+ and SO42− for the formation of iron-poor dolomite via sulfate reduction. From the Late Rhuddanian to the Mid-Aeronian, the Guangxi orogeny caused sea levels to fall, increasing water oxidation and reducing upwelling and volcanic activity, which lowered paleoproductivity. Rapid sedimentation rates, stepwise global temperature increases, and the intermittent intensification of weathering affected terrigenous clastic input, resulting in the alternating deposition of CRF, CRDF, and DQRF. Two favorable shale gas reservoirs were identified from the Rhuddanian–Aeronian period: Type I (BQRF) in the L1–L3 Layers, characterized by high TOC and brittleness, and Type II (DQRF) in the L4 Layer, with significant detrital quartz content. The Type I-favorable reservoir supports ongoing gas production, and the Type II-favorable reservoir offers potential as a future exploration target. Full article
(This article belongs to the Special Issue Environment and Geochemistry of Sediments, 2nd Edition)
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<p>(<b>a</b>) The Upper Yangtze platform’s position during the Rhuddanian–Aeronian period, adapted from [<a href="#B53-minerals-14-00949" class="html-bibr">53</a>]. (<b>b</b>) Geographical distribution of the Sichuan basin within China, adapted from [<a href="#B8-minerals-14-00949" class="html-bibr">8</a>]. (<b>c</b>) The distribution of the research area (Changning Block) in the Sichuan Basin, adapted from [<a href="#B33-minerals-14-00949" class="html-bibr">33</a>].</p>
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<p>Stratigraphic framework, mineral composition, sample locations, and lithofacies classification for the Rhuddanian–Aeronian stage of Well N1. GR—natural gamma ray logging; Mem.—Member; LMX. Fm.—Longmaxi Formation; WF. Fm.—Wufeng Formation.</p>
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<p>Mineral composition of four shale lithofacies developed in the Longmaxi Formation, N1 Well.</p>
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<p>QEMSCAN image characteristics of four typical lithofacies developed in the Longmaxi Formation, N1 Well. (<b>a</b>) Representative sample image for carbonate rich lithofacies (CRF), 2566.9 m. (<b>b</b>) Representative sample image for biogenic quartz-rich lithofacies (BQRF), 2576.76 m. (<b>c</b>) Representative sample detrital clay-rich lithofacies (CRDF), 2532.82 m. (<b>d</b>) Representative sample image for quartz-rich detrital lithofacies (QRDF), 2531.72 m.</p>
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<p>Thin-section images of representative shale samples from four lithofacies. (<b>a</b>) Abundant radiolarians with a diameter of approximately 50 μm developed in the BQRF shale sample, under plane-polarized light, 2576.08 m; (<b>b</b>,<b>c</b>) radiolarian shells filled with biogenic quartz, BQRF representative sample, under plane-polarized light and cross-polarized light, 2551.04 m; (<b>d</b>,<b>e</b>) anhedral, irregularly shaped, and variably sized detrital quartz grains irregularly distributed, with detrital clay dispersed throughout, under plane-polarized light and cross-polarized light, DQRF representative sample, 2556.61 m; (<b>f</b>) detrital siltstone clasts are well-developed in the QRDF sample, under plane-polarized light, 2563.24 m; (<b>g</b>,<b>h</b>) amorphous detrital clay minerals are diffusely distributed, under plane-polarized light and cross-polarized light, CRDF representative sample, 2579.74 m; (<b>i</b>) some detrital clay minerals are distributed in clumps, CRDF representative sample, under cross-polarized light, 2545.09 m; (<b>j</b>) blocky detrital calcite distributed between minerals, stained with alizarin red, under plane-polarized light, CRF representative sample, 2580.71 m; (<b>k</b>,<b>l</b>) detrital calcite and non-ferroan rhombohedral dolomite, under plane-polarized light and cross-polarized light, CRF representative sample, 2580.71 m.</p>
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<p>Scanning electron microscope images of representative samples of four lithofacies from the Rhuddanian–Aeronian period in Well N1. The marked points within the red circles in the scanning electron microscope (SEM) images represent the locations where energy-dispersive spectroscopy (EDS) data were collected. For detailed EDS data, please refer to <a href="#app1-minerals-14-00949" class="html-app">Table S1</a> (<b>a</b>) Siliceous biogenic debris coexists with biogenic microcrystalline quartz, BQRF representative sample, 2576.08 m; (<b>b</b>) pyritized sponge spicules in association with biogenic microcrystalline quartz, representative sample, 2551.04 m; (<b>c</b>) intergranular pores in biogenic microcrystalline quartz filled with organic matter, representative sample, 2559.72 m; (<b>d</b>) anhedral detrital quartz is relatively well-developed in the QRDF representative sample, with occasional bent and striped detrital clay observed, 2563.24 m; (<b>e</b>) irregularly shaped detrital quartz and detrital calcite with concavo-convex grain contacts, QRDF representative sample, 2556.61 m; (<b>f</b>) a large amount of detrital quartz and detrital calcite exhibit irregular contact with low euhedral degree, QRDF representative sample, 2555.29 m; (<b>g</b>) detrital clay minerals are significantly affected by compaction, resulting in oriented alignment, CRDF representative sample,2579.74 m; (<b>h</b>) densely packed detrital clay minerals filling intergranular pores, CRDF representative sample, 2551.75 m; (<b>i</b>) detrital clay deformed by compaction, bending and filling intergranular pores, CRDF representative sample, 2545.09 m; (<b>j</b>) syntaxial calcite cementation filling intergranular pores during syndiagenesis, CRF representative sample; (<b>k</b>) syndepositional calcite cement in a basal pattern filling the spaces between detrital quartz grains, CRF representative sample, 2580.71 m; (<b>l</b>) basal calcite cement filling intergranular pores with developed dissolution pores, CRF representative sample, 2578.08 m; (<b>h</b>) pyrite coexisting with early diagenetic non-ferroan dolomite, CRF representative sample, 2569.21 m. SS: sponge spicules; OM: organic matter; BQ: biogenic quartz; DC: detrital calcite; CC: calcite cement; DQ: detrital quartz; IPD: iron-poor dolomite; DCL: detrital clay; PY: pyrite.</p>
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<p>Vertical variation of geochemical characterization parameters in Well N1 for paleoenvironment during the Rhuddanian–Aeronian period. Mem.—Member; LMX. Fm.—Longmaxi Formation; GYQ—Guanyinqiao Member; WF. Fm.—Wufeng Formation; LX. Fm.—Linxiang Formation.</p>
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<p>Correlation plots of paleoredox indicators for seven layers during the Rhuddanian–Aeronian period in Well N1: (<b>a</b>) Ni/Co vs. U/Th; (<b>b</b>) Ni/Co vs. V/Cr.</p>
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<p>Plots illustrating water mass restriction levels across seven layers during the Rhuddanian–Aeronian transition in Well N1: (<b>a</b>) Mo-TOC relationships compared to modern anoxic stilled-basin environments; (<b>b</b>) Mo<sub>EF</sub> vs. U<sub>EF</sub>; (<b>c</b>) Co*Mn vs. Al; (<b>d</b>) TOC vs. Co*Mn.</p>
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<p>Correlation analysis of TOC with terrigenous detrital input indicators: (<b>a</b>) TOC vs. Ti; (<b>b</b>) TOC vs. Zr; (<b>c</b>) TOC vs. K; (<b>d</b>) TOC vs. Al.</p>
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<p>Weathering intensity diagrams: (<b>a</b>) A-CN-K weathering intensity plot; (<b>b</b>) ICV-CIA weathering degree plot. The CIA and ICV identification diagrams were modified in [<a href="#B50-minerals-14-00949" class="html-bibr">50</a>,<a href="#B58-minerals-14-00949" class="html-bibr">58</a>]. Ka: kaolinite; Chl: chlorite; Gi: gibbsite; Sm: smectite; Mu: muscovite; Pl: plagioclase (Pl); Kfs: k-feldspar; CIA: chemical index of alteration; ICV: index of compositional variability; A: content of Al<sub>2</sub>O<sub>3</sub>; CN: content of CaO + Na<sub>2</sub>O; K: content of K<sub>2</sub>O.</p>
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<p>Source discrimination diagrams of Si element in four shale lithofacies (modified from [<a href="#B10-minerals-14-00949" class="html-bibr">10</a>,<a href="#B11-minerals-14-00949" class="html-bibr">11</a>,<a href="#B12-minerals-14-00949" class="html-bibr">12</a>,<a href="#B13-minerals-14-00949" class="html-bibr">13</a>,<a href="#B14-minerals-14-00949" class="html-bibr">14</a>,<a href="#B15-minerals-14-00949" class="html-bibr">15</a>]). (<b>a</b>) TOC vs. Si<sub>xs</sub>; (<b>b</b>) Si vs. Zr.</p>
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<p>Schematic diagram of the relationship between paleogeographic environments and lithofacies types during the Rhuddanian–Aeronian period in Well N1. GR—natural gamma ray logging; Mem.—Member; LMX. Fm.—Longmaxi Formation; WF. Fm.—Wufeng Formation; CRF: carbonate rich lithofacies; BQRF: biogenic quartz-rich lithofacies; CRDF: detrital clay-rich lithofacies; QRDF: quartz-rich detrital lithofacies.</p>
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<p>Model diagram of the influence of paleoenvironmental changes on the formation processes of four lithofacies during the Rhuddanian–Aeronian period. CRF: carbonate-rich lithofacies; BQRF: biogenic quartz-rich lithofacies; CRDF: detrital clay-rich lithofacies; QRDF: quartz-rich detrital lithofacies; OM: organic matter.</p>
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22 pages, 49469 KiB  
Article
First Evidence of Reproductive Strategies in Cephalopods Preserved in Phosphate and Siderite Nodules from the Devonian of Uruguay
by Graciela Piñeiro, Magela Rodao and Pablo Núñez Demarco
Foss. Stud. 2024, 2(3), 223-244; https://doi.org/10.3390/fossils2030011 - 13 Sep 2024
Viewed by 2148
Abstract
Uruguayan ammonoids are preserved in phosphate and siderite nodules found at the basalmost tillite-like conglomerates of the San Gregorio Formation. This lithostratigraphic unit was deposited under glacial conditions and its age (as well as that of the nodules) has been highly debated because [...] Read more.
Uruguayan ammonoids are preserved in phosphate and siderite nodules found at the basalmost tillite-like conglomerates of the San Gregorio Formation. This lithostratigraphic unit was deposited under glacial conditions and its age (as well as that of the nodules) has been highly debated because glaciations were intermittent in Gondwana during the Late Paleozoic. Reef-builder organisms (e.g., Rugosa and Tabulata), goniatite and orthoceratid cephalopods, brachiopods, sponges, actinopterygians and other indeterminate gnatostomes, as well as fragmentary stems and roots of cf. Lycopsida are the most frequent fossils in the nodules. According to new biostratigraphic and paleoclimatic evidence, these taxa are representative of a reefal environment of a preliminary Devonian age including species that are common in the underlying Early Devonian (Emsian) Durazno Group. Among the ammonoid remains, more than 40 clusters of hatchling goniatites were found in the nodules. Each cluster contains a variable number of shells similar in shape to some of the adults also preserved within the nodules, representing a single species preserved at the same developmental stage (3 mm on size average). The strongly packed shells are enveloped by a substance with a different chemical composition and microstructure with respect to that of the nodule matrix, possibly indicating the presence of a gelatinous-like substance reminiscent of that secreted by the females of some extant cuttlefish and octopuses at the time of the egg spawn. Differing from previously described ammonoid accumulations, our clusters are unique in containing individuals of just a single species preserved in the same ontogenetic stage. That allows us to suggest that they represent a mode of reproduction in which hatchlings were morphologically similar to their parents and occupied the same habitat. Our results are thus one of the oldest known records of reproductive strategies in Paleozoic ammonoids and the phosphate and siderite nodules from the San Gregorio Formation are here classified as a new Konservat-Lagerstätte, which is the oldest known for South America. Full article
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<p>Map showing the distribution of the studied areas of the San Gregorio Formation of Uruguay in the vicinity of the San Gregorio de Polanco city along both the banks of the Negro River (Tacuarembó and Durazno Departments, red circle), and close to the Melo city in the Cerro Largo Department (black symbols) [<a href="#B1-fossstud-02-00011" class="html-bibr">1</a>,<a href="#B2-fossstud-02-00011" class="html-bibr">2</a>,<a href="#B6-fossstud-02-00011" class="html-bibr">6</a>]. The fossiliferous phosphate and siderite nodules described herein are limited to the former area.</p>
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<p>Basic stratigraphy of the nodule bearing San Gregorio Formation of Uruguay and the underlying Early Devonian Durazno Group. (<b>A</b>). Schematic stratigraphic section of one of the outcrops where we found the specimens described herein. The arrow points to the level where striate bedrock surfaces from glacier displacement were found. (<b>B</b>). Photograph of the basal level of tillites that contain the reworked fossiliferous nodules (head arrow). (<b>C</b>). Detail of the bedrock surface scratched by rocks embedded in glacial ice during glacier displacement. It is worth noting that these striae (yellow arrow) are stratigraphically above the tillites that are bringing the nodules, evidencing the periglacial and postglacial origin of these deposits. Scale: Engineer Sebastian Marmol.</p>
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<p>Photographs of early juvenile ammonoid clusters from the Devonian of Uruguay. (<b>A</b>). Specimen JMMO-IMT 0215 represents the largest cluster found (approximately 55 mm in length) and it shows the closely packed ammonoids shells embedded in a possible gelatinous substance that protected and feed the individuals before hatching [<a href="#B39-fossstud-02-00011" class="html-bibr">39</a>]. The ammonitellae average diameter at this stage is near 0.4 to 0.5 mm, and the shell has reached the three additional whorls that would characterize the hatchling phase outside the gelatinous envelope. Scale bar: 10 mm. (<b>B</b>,<b>C</b>). JMMO-IMT 0311. Part and counterpart of a cluster containing well-preserved, early juvenile tiny ammonoids, which allowed us to studied them by SEM and took good microphotographs of the initial chamber, as well as study the morphology that characterize the ammonitella stage for this new species of Uruguayan ammonoids (see <a href="#fossstud-02-00011-f007" class="html-fig">Figure 7</a> and <a href="#fossstud-02-00011-f008" class="html-fig">Figure 8</a>). Scale bars: 5 mm.</p>
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<p>JMMO-IMT 0230. Photograph of early juvenile ammonoid clusters from the Devonian of Uruguay. The image shows some shells inside a phosphate nodule of the San Gregorio Formation (Central Uruguay). Following [<a href="#B40-fossstud-02-00011" class="html-bibr">40</a>], a possible gelatinous substance enclosing the shells seems to have been broken, maybe representing the moment in which the individuals abandon it and escape to the water-column, or the image might show the thin gelatinous envelop unexpectedly broken by a strong environmental event or by a predator attack. Scale bar: 5 mm.</p>
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<p>Size variation in the shells (<b>a</b>) and ammonitella stage (<b>b</b>) recording at the ammonoid clusters found in phosphate and siderite nodules of the San Gregorio Formation of Uruguay. Measurements of the shells were taken from the best preserved specimens in dorsal view from eight clusters (MMO 0156, 171, 215, 225, 230, 304, 305, 311), trying to cover all the represented sizes, ranging from 3 to 5 mm in average. Measurements of diameters of the ammonitella stage were mostly allowed from the best preserved specimens studied by SEM and were taken following [<a href="#B36-fossstud-02-00011" class="html-bibr">36</a>,<a href="#B38-fossstud-02-00011" class="html-bibr">38</a>].</p>
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<p>Comparative chemical composition and microstructure of the substance that encloses the ammonoid early juvenile specimens herein studied with respect of that of the nodule matrix containing them. (<b>A</b>). SEM-EDS analysis of an area of the matrix in specimen JMMO-IMT 0215. The main elements are calcium and phosphorus, with a variable content of iron, which turns the nodules as phosphate or siderite according to the amount of Fe that they contain. (<b>B</b>). Typical composition found in the possible gelatinous substance that encloses the clusters. (<b>C1</b>,<b>C2</b>) are SEM-EDS analyses that show the high content of carbon that is found in the mentioned substance, denoting the high preservation of soft tissues.</p>
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<p>Microanatomy of the ammonitella stage of tiny ammonoid shells inside the clusters from the Devonian of Uruguay. (<b>A</b>). JMMO-IMT 0305. SEM images of one of the best-preserved shells in lateral view. The initial chamber is poorly delimited but the caecum is well identified. (<b>B</b>). Close up of other shell preserved in the same cluster (JMMO-IMT 0305) to show the internal morphology of the initial chamber well delimited by a septum that separates it from the beginning of the first whorl. (<b>C</b>,<b>D</b>). Other specimens from cluster JMMO-IMT 0304 also show the semicircular shape of the initial chamber and the caecum and prosiphon shapes. Abbreviations: c, caecum; ic, initial chamber; prs, proseptum; psi, prosiphon.</p>
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<p>(<b>A</b>). Dorsal view of the initial chamber and the first whorl showing the position and morphology of the proseptum and the second septum (small black arrow). (<b>B</b>). Close up of the proseptum and second septum shown in (<b>A</b>). (<b>C</b>). Ammonitella stage morphology of a specimen found in the cluster JMMO-IMT 0305, where can be seen that the ornamentation of the shell shows a gradual change at the level of what we interpreted is the proseptum 1. (<b>D</b>). Interpretive drawing of (<b>C</b>) at the same scale. Abbreviations: c, caecum, ic, initial chamber, prs, proseptum, psi, prosiphon.</p>
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<p>SEM images showing the morphology and configuration of the siphuncle and the siphuncular tube in the ammonitella ontogenetic stage of the best-preserved specimens in clusters from the Devonian of Uruguay. All specimens shown are part of the cluster JMMO-IMT 0311. (<b>A</b>). Almost complete specimen showing the siphuncle across the last whorl passing through the chambers close to the outer wall of the shell at the middle region of the chamber. Interestingly, it can be seen that the septum is deformed/opened both centrally and dorsally. (<b>B</b>–<b>D</b>). Images taken from different shells confirming the common configuration of the siphuncle by passing through the median opening formed by the septa, particularly clear in (<b>D</b>).</p>
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<p>Ornamentation of the external surface of the ammonitella and early juvenile stages in individual shells from clusters of the Devonian of Uruguay. (<b>A</b>). JMMO-IMT 0304. Photograph under Camera Lucida of part of the gelatinous substance covering the shells. An almost complete and well preserved specimen displays the lirae-like ornamentation across the shell. Note that it is very fine-ribbed at the first whorl, increasing the space between ribs in direction to the aperture. Scale bar: 30 mm. (<b>B</b>). JMMO-IMT 0304. SEM image where both the mold and the outer ornamentation of the ammonitella shell can be appreciated. (<b>C</b>). JMMO-IMT 0311. SEM photograph of one of the cluster components showing the faint lirae-like ornamentation pattern characterizing the first whorls of the phragmocone, which is different from the well marked ribs observed in the outermost whorls.</p>
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<p>Morphology of the suture in ammonoids preserved in siderite and phosphate nodules of the San Gregorio Formation, Devonian of Uruguay. (<b>A</b>): JMMO-IMT 0215, small ammonoid, possible early juvenile individual. (<b>B</b>). JMMO-IMT 0016, young adult individual. (<b>C</b>,<b>D</b>). JMMO-IMT 0092 and 0091, adult individuals. The pattern of the sutures is clearly related to the ontogenetic stage of the analyzed specimens. It seems to be not constant because the walls of the septa form three-dimensional folds that are more or less accentuated or possess more or less irregularities, depending on the height at which the specimen is sectioned. The sutures at the central chambers are not always visible, i.e., they are not always exposed if the cut does not pass exactly to the center of these sections. (<b>E</b>–<b>H</b>). Interpretive drawings of (<b>A</b>–<b>D</b>). (<b>I</b>). JMMO-IMT 0305. Interpretive drawing of the shell of one of the individuals that are components of the cluster showing the first four phragmocone cameral septa and the sutures for these septa, thus delimitating the end of the ammonitella shell (red arrow). (<b>J</b>). Photograph of the specimen drawn at I clearly showing the first septum (red arrow) delimitation the shape of the ammonitella stage. Scale bars: (<b>E</b>). 5 mm; (<b>F</b>–<b>H</b>). 10 mm; (<b>J</b>). 1 mm. See also <a href="#fossstud-02-00011-f008" class="html-fig">Figure 8</a> as a complement.</p>
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<p>Main taxa represented in the reef community preserved in siderite and phosphate nodules of the San Gregorio Formation, Devonian of Uruguay. (<b>A</b>). JMM-IMT 0006, Actinopterygii (skull and anterior region of the trunk). (<b>B</b>). JMM-IMT 0056. Ammonoidea (goniatite ammonoid adult associated to corallites of cf. Rugosa (arrow). (<b>C</b>). JMM-IMT 0331. Trilobita (characteristic red color and badly preserved; could be a molten exhubia). (<b>D</b>). JMM-IMT 0313. Brachiopoda (clusters of <span class="html-italic">Orbiculoidea baini</span>). (<b>E</b>). JMM-IMT 0234. Rugosa (colonial corallites). (<b>F</b>). JMMO-IMT 0380. Well-preserved coral specimen tentatively assigned to Tabulata, showing internal morphology of the wall (w) and trabeculate septal region (st). (<b>G</b>). JMM-IMT 0422 cf. Lycopsida stem or root. (<b>H</b>,<b>I</b>). JMM-IMT165. Cephalopoda Orthoceridae. Fragmentary cone-shaped shell of a nautiloid cephalopod. Scale bars: (<b>A</b>–<b>C</b>,<b>E</b>–<b>G</b>): 10 mm; (<b>D</b>): 3 mm; and (<b>H</b>–<b>I</b>): 20 mm.</p>
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11 pages, 1893 KiB  
Article
Unique Jurassic Ovaries Shed a New Light on the Nature of Carpels
by Qiang Fu, Jie Sun, Shaolin Zheng and Xin Wang
Plants 2024, 13(16), 2239; https://doi.org/10.3390/plants13162239 - 12 Aug 2024
Viewed by 1035
Abstract
Enclosed ovules are a reproductive feature restricted to angiosperms. Although this feature can be used as a criterion for identifying fossil angiosperms, how ovules are enclosed and the nature of the placenta are still foci of debates. A reason underlying these controversies is [...] Read more.
Enclosed ovules are a reproductive feature restricted to angiosperms. Although this feature can be used as a criterion for identifying fossil angiosperms, how ovules are enclosed and the nature of the placenta are still foci of debates. A reason underlying these controversies is the lack of reproductive organ fossils shedding light on these issues. These controversies hinder a clear understanding of angiosperm evolution and systematics. Here, we report a new fossil ovary, Xenofructus dabuensis gen. et sp. nov, from the Middle Jurassic of Liaoning, China. Our fossil clearly demonstrates the existence of ovules in Xenofructus that has a free central placentation. This new feature implies that a placenta in angiosperm gynoecia is homologous to an ovule/seed-bearing axis, and free central placentation is one of the early developed placentations. This discovery is apparently at odds with the current understanding of placentation and its evolution. Apparently, the understanding of angiosperms and their gynoecia should be updated with newly available palaeobotanical data. Full article
(This article belongs to the Special Issue Inflorescence Architecture and Development in Plants)
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<p><span class="html-italic">Xenofructus dabuensis</span> gen. et sp. nov and its details. Specimen number KP10-18A. (<b>a</b>). Holotype, showing the profile of Ovary A and its seeds/ovules exposed after the foreground ovary is removed. Scale bar = 1 mm. (<b>b</b>). Ovary B and its internal ovules partially exposed and partially covered by the broken ovary wall. Scale bar = 1 mm. (<b>c</b>). Detailed view of the black rectangle in (<b>b</b>), showing three ovules (s) of variable shapes and ovary wall (upper right) covering other ovules. Scale bar = 1 mm. (<b>d</b>). Detailed view of the rectangle in (<b>a</b>), showing robust abaxial margin (between the triangles) of the ovary. Scale bar = 1 mm. (<b>e</b>). Broken ovary wall (upper right) and exposed internal of the ovary (lower left), and the boundary in between (triangles), enlarged from the white rectangle in (<b>b</b>). Scale bar = 0.5 mm. (<b>f</b>). A sickle-shaped ovule with a distal invagination (possible micropyle, triangle), enlarged from the rectangle in (<b>c</b>). Scale bar = 1 mm. (<b>g</b>). A micro-CT rendering of the specimen showing two ovaries parallel deployed on the surface of the specimen. (<b>h</b>–<b>j</b>). Serial sections of Ovary B, showing the ovule-bearing placenta (triangles) independent from both margins of the ovary. Scale bar = 2 mm.</p>
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<p>Sketches of two <span class="html-italic">Xenofructus</span> ovaries. The ovary outline is in black, while the seed outline is in red. (<b>a</b>). The ovary in <a href="#plants-13-02239-f001" class="html-fig">Figure 1</a>a. (<b>b</b>). The ovary in <a href="#plants-13-02239-f001" class="html-fig">Figure 1</a>b.</p>
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<p>Several representatives of early angiosperms, showing variable placentations in the fruits/ovaries of early angiosperms. Seeds (S)/ovules (O) are inserted either along the adaxial (AD), abaxial (AB), or both margins of a fruit/ovary, or are basally fixed in a fruit/ovary. 1. <span class="html-italic">Archaefructus</span>, according to Wang and Zheng [<a href="#B19-plants-13-02239" class="html-bibr">19</a>]; 2. <span class="html-italic">Xenofructus</span>; 3. <span class="html-italic">Qingganninginfructus</span>, according to Han et.al. [<a href="#B36-plants-13-02239" class="html-bibr">36</a>]; 4. <span class="html-italic">Gansufructus</span>, according to Du et al. [<a href="#B57-plants-13-02239" class="html-bibr">57</a>]; 5. <span class="html-italic">Sinocarpus</span>, according to Leng and Friis [<a href="#B55-plants-13-02239" class="html-bibr">55</a>]; 6. <span class="html-italic">Archaeanthus</span>, according to Wang [<a href="#B20-plants-13-02239" class="html-bibr">20</a>].</p>
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10 pages, 2764 KiB  
Communication
Shaolinia: A Fossil Link between Conifers and Angiosperms
by Xin Wang and Li-Jun Chen
Plants 2024, 13(15), 2162; https://doi.org/10.3390/plants13152162 - 5 Aug 2024
Viewed by 1441
Abstract
The flowering plants (angiosperms) are the dominant and defining group of the Earth ecosystems today. However, from which group and by what way flowers, especially their gynoecia (the key characteristic organs of angiosperms), are derived have been key questions in botany, and have [...] Read more.
The flowering plants (angiosperms) are the dominant and defining group of the Earth ecosystems today. However, from which group and by what way flowers, especially their gynoecia (the key characteristic organs of angiosperms), are derived have been key questions in botany, and have remained unanswered despite botanists’ efforts over centuries. Such an embarrassing situation can be attributed to the lack of plants with partially enclosed ovules, which are supposed fill a position between gymnosperms and angiosperms. Here, we report a fossil plant that has apparent coniferous vegetative and reproductive characters but has a single seed partially wrapped by the subtending bract. Such a morphology suggests that a carpel of some angiosperms is equivalent to a lateral appendage (a bract plus its axillary seed) of this fossil. Such a non-traditional interpretation of the homology of angiosperm carpels is compatible with various new progresses made in botany and is in line with Tomlinson’s recent hypothesis. Together with other fossil evidence reported recently, it appears that gynoecia in angiosperms are derived in multiple ways. Full article
(This article belongs to the Special Issue Inflorescence Architecture and Development in Plants)
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<p>General view of <span class="html-italic">Shaolinia intermedia</span> gen. et sp. nov. (<b>A</b>,<b>B</b>) Two counterparts of the same specimen, showing several axillary branches (arrows), leaves and four cone-like reproductive organs (1–4) arranged along the branch. Scale bar = 1 cm.</p>
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<p>Leaves and reproductive organs of <span class="html-italic">Shaolinia intermedia</span>. (<b>A</b>) The distal portion of the branch with helically arranged leaves. Scale bar = 2 mm. (<b>B</b>) Detailed view of the reproductive organs (Nos. 2 and 4). Note the helically arrange lateral appendages. Scale bar = 2 mm. (<b>C</b>) Detailed view of reproductive organ No. 3, with helically arranged lateral appendages. Scale bar = 2 mm. (<b>D</b>) Detailed view of reproductive organ No. 2, showing seeds inside the lateral appendages. Scale bar = 2 mm. (<b>E</b>) Detailed view of the distal portion of the reproductive organ shown in (<b>C</b>). The arrowed seed is removed and shown in (<b>F</b>,<b>G</b>) and <a href="#plants-13-02162-f004" class="html-fig">Figure 4</a>A–D. Scale bar = 1 mm. (<b>F</b>,<b>G</b>) Detailed views of the seed removed from the organ shown in (<b>E</b>). Scale bar = 0.1 mm.</p>
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<p>Lateral appendages with in situ seed inside and an adaxial gap. (<b>A</b>) Detailed side view of lateral appendage No. 3 in <a href="#plants-13-02162-f002" class="html-fig">Figure 2</a>C, showing the seed (s) wrapped by the bract (b). Scale bar = 0.5 mm. (<b>B</b>) Detailed side view of top lateral appendage in <a href="#plants-13-02162-f002" class="html-fig">Figure 2</a>C, showing the adaxial gap with two margins (arrows) of the bract. Scale bar = 0.5 mm.</p>
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<p>SEM view of the <span class="html-italic">in situ</span> seed found in <span class="html-italic">Shaolinia intermedia</span>, from the reproductive organ No. 2 shown in <a href="#plants-13-02162-f002" class="html-fig">Figure 2</a>C,E–G. (<b>A</b>) Seed in whole. Scale bar = 0.1 mm. (<b>B</b>) Converging cellular arrangement suggestive of possible micropyle (arrow) of the seed. Scale bar = 0.1 mm. (<b>C</b>) Seed coat sculpture. Scale bar = 10 μm. (<b>D</b>) Detailed cellular view of the seed coat sculpture. Scale bar = 10 μm.</p>
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<p>Sketches of the lateral appendages of <span class="html-italic">Shaolinia intermedia</span> showing spatial relationship between subtending bract and axillary seed. Not to scale. (<b>A</b>) Longitudinal radial profile of a lateral appendage showing a bract and an adaxial seed attached to the central axis and partially wrapped. The position of (<b>C</b>) is marked. (<b>B</b>) Adaxial view of a lateral appendage showing a bract and a partially wrapped adaxial seed inside. Note the adaxial gap of the bract and micropyle on the right side of the ovule. The positions of (<b>A</b>,<b>C</b>) are marked. (<b>C</b>) Cross view of a lateral appendage showing a bract and an axillary partially wrapped adaxial seed. The position of (<b>A</b>) is marked.</p>
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15 pages, 3667 KiB  
Article
Characteristics of Clay Minerals in Sediments of Xinghua Bay and Nanri Channel in Fujian Province and Their Paleoenvironmental Significance
by Xin Li, Jinrong Wang, Ke Yin, Qin Chen, Wei Liu, Yanna Huang, Yongchao Wang, Zhishan Wu and Jiansui Lin
J. Mar. Sci. Eng. 2024, 12(8), 1270; https://doi.org/10.3390/jmse12081270 - 29 Jul 2024
Viewed by 604
Abstract
Under the background of global climate change, the evolution of climate in the future is the focus of geoscience. The Nanri Channel is an important passage connecting the Xinghua Bay and the Taiwan Strait, in China, and the study of its provenance and [...] Read more.
Under the background of global climate change, the evolution of climate in the future is the focus of geoscience. The Nanri Channel is an important passage connecting the Xinghua Bay and the Taiwan Strait, in China, and the study of its provenance and paleoenvironmental alternation is of great significance to the climate evolution in the eastern coast of China. The grain size and X-ray diffraction analyses of sediments from ZK1 in Nanri Channel and ZK5 in Xinghua Bay, were used to study the variation of grain size and clay mineral characteristics and to analyze the changes in hydrodynamic characteristics, provenance, and paleoenvironmental evolution in the regions since the Last Glacial Maximum. The results show that the sedimentary environment of ZK1 varies from the nearshore tidal flat facies with strong hydrodynamic conditions and the neighboring rivers as the main provenance, to the littoral facies with weak hydrodynamic conditions and the Yangtze River-like type sediments as the main provenance. The sedimentary environment of ZK5 is from the nearshore tidal flat facies with strong hydrodynamic conditions to the littoral facies with weak hydrodynamic conditions, and the provenance of both facies is mainly Yangtze River-like type sediments. The clay mineral characteristics of ZK1 show that the climate in the Nanri Channel has experienced a change from cool and wet, to mild and dry, to mild and wet since the Last Glacial Maximum, while the climate in the Xinghua Bay has experienced a change from warm and humid, to moderate and dry, to warm and humid since the early-middle Holocene, which provides scientific theoretical support for the provenance and paleoenvironment of sediments in the study area and neighboring areas. Full article
(This article belongs to the Section Geological Oceanography)
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<p>(<b>a</b>) Geographic map of the study area, showing the Taiwan warm current and Zhejiang and Fujian coastal current. (<b>b</b>) Column sample location map. Dark blue dots denote the core location. Map drawn with Ocean Data View.</p>
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<p>Triangulation of ZK1 and ZK5 sediment grain size classification. (<b>a</b>) ZK1, the black squares; (<b>b</b>) ZK5, the blue squares.</p>
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<p>Grain size characteristics of columnar sediments in Nanri Channel and Xinghua Bay. (<b>a</b>) ZK1 in Nanri Channel; (<b>b</b>) ZK5 in Xinghua Bay. The red arrow represents the age of the sediments at the depth in column sample.</p>
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<p>Characterization of the variation of the content of ZK1 clay minerals. The red arrow represents the age of the sediments at the depth in column sample.</p>
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<p>Characterization of the variation of the content of ZK5 clay minerals. The red arrow represents the age of the sediments at the depth in column sample.</p>
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<p>Hydrodynamic and sedimentation relationship of ZK1 and ZK5.</p>
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<p>Comparison of clay mineral fractions of sediments in the study area from each potential source area. (A): Yangtze River-like sediments; (B): Yellow River-like sediments; (C): Taiwan-like sediments.</p>
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<p>Cluster analysis diagram of clay mineral fractions of sediments in the study area from each potential source area [<a href="#B18-jmse-12-01270" class="html-bibr">18</a>,<a href="#B19-jmse-12-01270" class="html-bibr">19</a>,<a href="#B20-jmse-12-01270" class="html-bibr">20</a>,<a href="#B21-jmse-12-01270" class="html-bibr">21</a>,<a href="#B22-jmse-12-01270" class="html-bibr">22</a>,<a href="#B23-jmse-12-01270" class="html-bibr">23</a>,<a href="#B24-jmse-12-01270" class="html-bibr">24</a>,<a href="#B25-jmse-12-01270" class="html-bibr">25</a>,<a href="#B26-jmse-12-01270" class="html-bibr">26</a>,<a href="#B27-jmse-12-01270" class="html-bibr">27</a>,<a href="#B28-jmse-12-01270" class="html-bibr">28</a>,<a href="#B29-jmse-12-01270" class="html-bibr">29</a>,<a href="#B30-jmse-12-01270" class="html-bibr">30</a>,<a href="#B31-jmse-12-01270" class="html-bibr">31</a>,<a href="#B32-jmse-12-01270" class="html-bibr">32</a>,<a href="#B33-jmse-12-01270" class="html-bibr">33</a>].</p>
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16 pages, 5734 KiB  
Article
Elemental Geochemistry on Paleoenvironment Reconstruction: Proxies on Miocene-Pliocene of Marine to Fluvial Sediment in Serpong, Banten, Indonesia
by Heri Syaeful, Syaiful Bakhri, Budi Muljana, Agus Sumaryanto, I. Gde Sukadana, Hendra Adhi Pratama, Adi Gunawan Muhammad, Ngadenin, Frederikus Dian Indrastomo, Roni Cahya Ciputra, Susilo Widodo, Nunik Madyaningarum, Puji Santosa, Muhammad Burhannudinnur and Zufialdi Zakaria
Geosciences 2024, 14(7), 189; https://doi.org/10.3390/geosciences14070189 - 13 Jul 2024
Viewed by 763
Abstract
Research of the depositional environment using geological mapping, petrography, gamma-ray (GR) log, palynology, and foraminifera fossils of the Bojongmanik Formation has led to the formation of several different conclusions about the transition to the marine environment, which are attractive to revisit. The expected [...] Read more.
Research of the depositional environment using geological mapping, petrography, gamma-ray (GR) log, palynology, and foraminifera fossils of the Bojongmanik Formation has led to the formation of several different conclusions about the transition to the marine environment, which are attractive to revisit. The expected results of this research are to determine the paleoenvironment of the Bojongmanik and Serpong Formations based on elemental geochemistry, the development of paleoenvironment proxies based on portable X-ray fluorescence (pXRF) in fluvial to transitional environments studies, and the contribution of paleoenvironment analysis to GR-log facies interpretation. The research methodology starts with GR-log facies analysis, Pearson’s correlation, paleoenvironment analysis based on elemental affinity and elemental ratio, and comparing the paleoenvironment with GR-log-based facies. The paleoenvironment analysis based on elemental geochemistry resulted in the Bojongmanik Formation in the research area deposited at the tidal point bar, lagoon, and shoreface, while the Serpong Formation was deposited at the fluvial point bar and floodplain. Compared to previous research, the Bojongmanik Formation in the research area could be stratigraphically related to the upper Bojongmanik Formation. Proxies based on elemental geochemical affinities of carbonate-associated, carbonate-productivity, terrigenous-associated elements, and redox-sensitive trace elements show contrast changes between facies. Proxies based on the specific ratio show a detailed paleoenvironment for paleoclimate (Sr/Cu), paleosalinity (Sr/Ba), paleoredox (Cu/Zn), paleo-hydrodynamics and water depth (Zr/Rb and Fe/Mn), sediment provenance (Cr/Zr), and siliciclastic-dominated (Zr + Rb)/Sr. Adding a geochemistry element-based paleoenvironment analysis benefits from a more specific justification for GR-log facies interpretation. Full article
(This article belongs to the Section Geochemistry)
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<p>Distribution of Bojongmanik and Serpong Formations surrounding the research area (black box).</p>
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<p>GR-log facies analysis of DH-11.</p>
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<p>Drill core and facies unit of DH-11.</p>
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<p>Paleoenvironment analysis based on elemental affinity. Note: The arrow shows the enriched zone.</p>
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<p>Paleoenvironment analysis based on elemental ratio. Note: the red dashed line is the threshold from previous research, and the yellow dashed line is defined in this research.</p>
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<p>Paleoenvironmental change from the tidal point bar to the fluvial point bar (<b>a</b>,<b>b</b>) and from the upper shoreface to the tidal point bar (<b>c</b>,<b>d</b>).</p>
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<p>Box plot of the result of paleoenvironment reconstruction from (Zr + Rb)/Sr (<b>a</b>) and Cu/Zn (<b>b</b>). The vertical dashed line indicates the boundary of the depositional environment, while the horizontal dashed line indicates the threshold value between the marine and fluvial environments.</p>
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14 pages, 9677 KiB  
Article
Holocene Paleoclimate Changes around Qinghai Lake in the Northeastern Qinghai-Tibet Plateau: Insights from Isotope Geochemistry of Aeolian Sediment
by Qiang Peng, Chongyi E, Xiangzhong Li, Yongjuan Sun, Jing Zhang, Shuaiqi Zhang, Yunkun Shi, Xianba Ji and Zhaokang Zhang
Atmosphere 2024, 15(7), 833; https://doi.org/10.3390/atmos15070833 - 12 Jul 2024
Cited by 1 | Viewed by 700
Abstract
The stable carbon isotope composition of total organic matter (δ13Corg) has been utilized in aeolian sediments, serving as an indicator for reconstructing terrestrial paleoenvironments. The Qinghai Lake (QHL) Basin is a climate-sensitive region of significant importance in paleoclimatic reconstruction. [...] Read more.
The stable carbon isotope composition of total organic matter (δ13Corg) has been utilized in aeolian sediments, serving as an indicator for reconstructing terrestrial paleoenvironments. The Qinghai Lake (QHL) Basin is a climate-sensitive region of significant importance in paleoclimatic reconstruction. However, the reconstructed climatic variations based on δ13Corg in aeolian sediments in the QHL Basin in the northeastern Qinghai-Tibet Plateau (QTP) are lacking, and their paleoclimatic significance remains poorly understood. By conducting δ13Corg measurements on the Niaodao (ND) aeolian profile near QHL, we reconstructed the paleoclimate changes of 11 ka–present. The variation range of the δ13Corg values in the ND profile indicated the terrestrial ecosystems were not the sole contributor to lacustrine organic matter. The δ13Corg values are an indicator of historical temperature changes in the study area, exhibiting similar trends with the reconstruction of Chinese summer temperatures, East Asian air temperature, global temperature, and Northern Hemisphere summer insolation at 37° N. The temperature increased with high frequency and amplitude oscillations, with strong aeolian activity and low total organic carbon accumulation during the Early Holocene. The temperature was maintained at a high and stable level, with the weakest aeolian activity and intensified pedogenesis during the Middle Holocene. The temperature decreased at a high rate, with renewed aeolian activity and weak pedogenesis during the Late Holocene. Full article
(This article belongs to the Special Issue Paleoclimate Changes and Dust Cycle Recorded by Eolian Sediments)
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<p>Map of the study area. The Qinghai-Tibet Plateau (QTP) is located in Central Asia, and the Qinghai Lake (QHL) Basin is located in the northeastern QTP, as indicated by the inset map. The red pentagon on the map denotes the location of the Niaodao (ND) profile examined in this study.</p>
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<p>Stratigraphy and dating of the ND profile, with the age scale of the profile referenced to [<a href="#B20-atmosphere-15-00833" class="html-bibr">20</a>]; the ND profile is located along the Buha River.</p>
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<p>Experimental procedures for the δ<sup>13</sup>C<sub>org</sub> sample.</p>
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<p>Data results are correlated with the age of the ND profile. (<b>a</b>) δ<sup>13</sup>C<sub>org</sub> and (<b>b</b>) total organic carbon (TOC).</p>
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<p>Numerical comparison of the δ<sup>13</sup>C<sub>org</sub> (<b>A</b>) and TOC (<b>B</b>) in terrestrial (ND profile and ZYC profile) and lacustrine sediments (Genggahai Lake and QHL).</p>
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<p>Comparison of the δ<sup>13</sup>C<sub>org</sub> in the ND profile of QHL with other indicators during the Holocene. (<b>a</b>) The δ<sup>13</sup>C<sub>org</sub> of the ND profile, (<b>b</b>) the quantitative precipitation reconstruction of QHL [<a href="#B39-atmosphere-15-00833" class="html-bibr">39</a>], (<b>c</b>) the summer temperature of QHL [<a href="#B47-atmosphere-15-00833" class="html-bibr">47</a>], (<b>d</b>) the reconstruction of summer temperature of China [<a href="#B49-atmosphere-15-00833" class="html-bibr">49</a>], (<b>e</b>) the East Asian air temperature [<a href="#B48-atmosphere-15-00833" class="html-bibr">48</a>], and (<b>f</b>) the global temperature [<a href="#B50-atmosphere-15-00833" class="html-bibr">50</a>].</p>
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<p>Comparison of the δ<sup>13</sup>C<sub>org</sub> in the ND profile of QHL with other indicators since the Holocene. (<b>a</b>) The δ<sup>13</sup>C<sub>org</sub> of the ND profile, (<b>b</b>) the Northern Hemisphere summer insolation at 37° N [<a href="#B52-atmosphere-15-00833" class="html-bibr">52</a>], (<b>c</b>) the TOC, (<b>d</b>) low-frequency magnetic susceptibility (χlf), and (<b>e</b>) median grain size (Mz) of the ND profile. (<b>d</b>,<b>e</b>) Have been published in detail in the literature [<a href="#B20-atmosphere-15-00833" class="html-bibr">20</a>].</p>
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12 pages, 12874 KiB  
Article
New Evidence for an Episode of Accelerated Environmental Change in the Late Barremian: Geochemical and Paleontological Records from the Subbetic Basin (Western Tethys)
by Ginés A. de Gea, José Manuel Castro, Miguel Company, Luis O’Dogherty, José Sandoval, María Luisa Quijano, Cristina Sequero, Sandro Froehner and Roque Aguado
Geosciences 2024, 14(7), 187; https://doi.org/10.3390/geosciences14070187 - 11 Jul 2024
Viewed by 767
Abstract
We investigate a new event of accelerated environmental change that was recorded during the late Barremian in the pelagic Subbetic Basin (Western Tethys). Two pelagic sections have been studied using a multi-proxy approach based on C-isotope stratigraphy and a high-resolution quantitative study of [...] Read more.
We investigate a new event of accelerated environmental change that was recorded during the late Barremian in the pelagic Subbetic Basin (Western Tethys). Two pelagic sections have been studied using a multi-proxy approach based on C-isotope stratigraphy and a high-resolution quantitative study of nannofossil assemblages, along with major and trace elements and biomarkers. Our results provide a detailed biostratigraphy and C-isotope stratigraphy, and outline the paleoenvironmental conditions recorded during the early stages of the Taxy Episode. A disturbance has been identified in the C-isotope record, called the IFeNE (Intra-Feradianus negative C-excursion), which is coeval with environmental and biotic changes that predate the well-known ISNE (Intra-Sarasini negative C-excursion). The combined analysis of nannofossil associations, C-isotopes, major and trace elements, and biomarker distributions indicates a separate episode of warming heralding the ISNE, resulting in the acceleration of the hydrological cycle and a consequent increase in continental inputs and the fertilization of surface waters. The origin of the Taxy Episode (the IFeNE and ISNE) has been related to orbital factors (high-eccentricity cycles), and to a global increase in volcanism, probably related to the early phases of the Ontong Java Plateau. Full article
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<p>Geologic map of the eastern Betic Cordillera showing the locations of the sections studied. (A) Barranco de Cavila section (X.Kv2), (B) Rio Argos section (X. AG6). Modified from [<a href="#B10-geosciences-14-00187" class="html-bibr">10</a>].</p>
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<p>Paleogeography of the studied sections. See text for explanations [<a href="#B4-geosciences-14-00187" class="html-bibr">4</a>,<a href="#B14-geosciences-14-00187" class="html-bibr">14</a>,<a href="#B15-geosciences-14-00187" class="html-bibr">15</a>].</p>
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<p>Correlations of the sections studied with C-isotope stratigraphy and bioevents. Orenge band correspond to the stratigraphic IFeNE interval. ND is the Nannoconid Decline Event. Time scale is from [<a href="#B22-geosciences-14-00187" class="html-bibr">22</a>].</p>
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<p>Barranco de Cavila section (X.Kv2). C-isotope stratigraphy and nannofossil indices.</p>
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<p>Rio Argos section (X.Ag6). C-isotope stratigraphy and nannofossil indices.</p>
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<p>Rio Argos section (X.Ag6). C-isotope stratigraphy elemental geochemistry and biomarker ratios.</p>
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<p>Barranco de Cavila section (X.Kv2). C-isotope stratigraphy and elemental geochemistry.</p>
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39 pages, 33558 KiB  
Article
The Perizonium Ultrastructure, Divided Apical Pore Fields, Various Pore Occlusions and Visible Intermissio of Cymbella (Bacillariophyceae) with Descriptions of Four New Species
by Bin Yang, Bing Liu, Saúl Blanco and Patrick Rioual
Plants 2024, 13(13), 1851; https://doi.org/10.3390/plants13131851 - 5 Jul 2024
Viewed by 672
Abstract
The initial valves of two Cymbella species are observed under a scanning electron microscope, and the perizonium ultrastructure of Cymbella is revealed for the first time. The perizonium is composed of alternate nodes and internodes and lacks transverse perizonium bands. Four new species, [...] Read more.
The initial valves of two Cymbella species are observed under a scanning electron microscope, and the perizonium ultrastructure of Cymbella is revealed for the first time. The perizonium is composed of alternate nodes and internodes and lacks transverse perizonium bands. Four new species, Cymbella apiculatophora sp. nov., C. hunanensis sp. nov., C. juglandis sp. nov. and C. menyuanensis sp. nov., are described using light and scanning electron microscopy based on epilithon samples collected from rivers in Hunan and Qinghai Provinces, China. Cymbella menyuanensis is a typical Cymbella species that closely resembles species in the group around C. cymbiformis Agardh, the type species of the genus. Cymbella apiculatophora is similar to C. sinensis Metzeltin & Krammer, while Cymbella hunanensis is closer to the C. hustedtii Krasske group. The last species, C. juglandis, has a cymbelloid valve outline, an obscured intermissio, internal occlusions of the areolae, dorsally deflected distal raphe fissures and a divided apical pore field at each apex, and it does not appear to belong to any group. In addition, new observations on C. cf. excisiformis Krammer and C. hustedtii are reported. The current concept of the genus Cymbella does not represent a monophyletic group as shown by molecular phylogenetic analyses. However, these analyses are still at the preliminary stage and are not yet sufficient to support a complete revision of the genus. Thus, although extremely diverse ultrastructural features are observed in the six Cymbella species investigated in this paper, we prefer to keep them within Cymbella at this moment for the sake of nomenclatural stability. Full article
(This article belongs to the Section Plant Systematics, Taxonomy, Nomenclature and Classification)
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Figure 1

Figure 1
<p><span class="html-italic">Cymbella apiculatophora</span> sp. nov., LM. (<b>A</b>,<b>B</b>). Two uncleaned cells. (<b>C</b>–<b>K</b>). Nine valves showing a size diminution series; note one shortened stria on the dorsal middle part (arrows in <b>C</b>,<b>D</b>,<b>E</b>,<b>F</b>, respectively) and the apiculate apices. (<b>I</b>). Illustration of the holotype specimen. Scale bars (<b>A</b>,<b>B</b>) = 10 μm, (<b>C</b>–<b>K</b>) = 10 μm.</p>
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<p><span class="html-italic">Cymbella apiculatophora</span> sp. nov., SEM, valve external view. (<b>A</b>). A frustule. (<b>B</b>). Middle part details; note ca. 5 stigmata (five arrowheads) and rounded or dumbbell-like (three arrows) outer openings of areolae. (<b>C</b>,<b>D</b>). Details of two apices from <b>A</b>; note the apical field divided by the distal raphe fissure into two unequal areas—a larger area (LA) and a smaller area (SA)—and the rounded outer openings of areolae near each apex. (<b>E</b>,<b>F</b>). Two other middle part details; note ca. 5 stigmata (five arrowheads) and the rounded or dumbbell-like (four arrows) outer openings of areolae. Scale bars (<b>A</b>) = 10 μm, (<b>B</b>–<b>F</b>) = 2 μm.</p>
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<p><span class="html-italic">Cymbella apiculatophora</span> sp. nov., SEM, valve internal view. (<b>A</b>,<b>B</b>). Two valves; note a shortened stria on the dorsal middle part (two arrows). (<b>C</b>,<b>D</b>). Middle part details, note ca. 4 or 5 stigmata (arrowheads) and obscured intermissio (two arrows, respectively). (<b>E</b>). Apical detail; note the apical field divided by the distal raphe fissure into two unequal areas: a larger area (LA) and a smaller area (SA). (<b>F</b>). Apical detail; note the columns of V-shaped occlusions (three arrows). Scale bars (<b>A</b>,<b>B</b>) = 10 μm, (<b>C</b>) = 2 μm, (<b>D</b>–<b>F</b>) = 1 μm.</p>
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<p><span class="html-italic">Cymbella apiculatophora</span> sp. nov., SEM. (<b>A</b>–<b>C</b>). Details showing open girdle bands and a row of large, elongated pores located along the midline of copula (two arrows, respectively). (<b>D</b>–<b>F</b>). Internal details; note manhole-shaped internal openings (arrows) and their rounded to oblong silica closing plates (wavy arrows). Scale bars (<b>A</b>–<b>C</b>) = 2 μm, (<b>D</b>–<b>F</b>) = 1 μm.</p>
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<p><span class="html-italic">Cymbella</span> cf. <span class="html-italic">excisiformis</span>, LM. (<b>A</b>–<b>I</b>). Nine pre-normal valves; note that their somewhat vaulted outline. (<b>J</b>–<b>R</b>). Nine normal vegetative valves. Scale bar (<b>A</b>–<b>R</b>) = 10 μm.</p>
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<p><span class="html-italic">Cymbella</span> cf. <span class="html-italic">excisiformis</span>, pre-normal valve, SEM, external view. (<b>A</b>). A complete pre-normal valve. (<b>B</b>–<b>D</b>). Details from <b>A</b>. Note lineolate areola openings; most of them are oriented parallel to the apical axis, but some are oriented transapically or at an angle relative to the apical axis (arrows). Scale bars (<b>A</b>) = 10 μm, (<b>B</b>–<b>D</b>) = 2 μm.</p>
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<p><span class="html-italic">Cymbella</span> cf. <span class="html-italic">excisiformis</span>, SEM, external view. (<b>A</b>). A complete valve; note the lateral-reverse proximal raphe fissures. (<b>B</b>). Detail of middle part; note the stigma (arrow). (<b>C</b>,<b>D</b>). Two apical details; note that the distal raphe fissure does divide the apical pore field into two areas (arrows). Scale bars (<b>A</b>) = 10 μm, (<b>B</b>–<b>D</b>) = 2 μm.</p>
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<p><span class="html-italic">Cymbella</span> cf. <span class="html-italic">excisiformis</span>, SEM, internal view. (<b>A</b>). A complete valve. (<b>B</b>). Detail of middle part; note the stigma (arrow) and obscured intermissio (wavy arrow). (<b>C</b>,<b>D</b>). Two apical details; note an undulate flap-like silica strip covering the internal apertures of each column of foramina but not occluding the apertures completely (two arrows, respectively). Scale bars (<b>A</b>) = 10 μm, (<b>B</b>–<b>D</b>) = 2 μm.</p>
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<p><span class="html-italic">Cymbella hunanensis</span>, sp. nov., LM. (<b>A</b>–<b>N</b>). Fourteen valves in a series of diminishing size; note that a shortened stria is sometimes present on the dorsal central part (arrows). (<b>A</b>). Illustration of the holotype specimen. Scale bar (<b>A</b>–<b>N</b>) = 10 μm.</p>
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<p><span class="html-italic">Cymbella hunanensis</span>, sp. nov., SEM, external view. (<b>A</b>–<b>C</b>). Three valves; note that a shortened stria is sometimes present on the dorsal central part (arrow in <b>B</b>). (<b>D</b>). Middle part details; note the reniform closing plates (black arrows) and absence of a stigma. (<b>E</b>,<b>F</b>). Details of two apices from <b>C</b>. Note the apical field divided by the distal raphe fissure into two areas: a larger area (LA) and a small area (SA). Scale bars (<b>A</b>–<b>C</b>) = 10 μm, (<b>D</b>–<b>F</b>) = 1 μm.</p>
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<p><span class="html-italic">Cymbella hunanensis</span>, sp. nov., SEM, internal view. (<b>A</b>). A complete valve. (<b>B</b>). Middle part details; note the two internal proximal raphe endings interrupted by the central nodule (two arrows) and the absence of stigmata. (<b>C</b>,<b>D</b>). Apical details. Note the apical field divided into two areas: a large area (LA) and a small area (SA). (<b>E</b>). Other middle part details; note the two internal proximal raphe endings interrupted by the central nodule (two arrows) and the absence of stigmata (arrows). (<b>F</b>). Details showing an undulate flap-like silica strip above the internal apertures of each column of foramina but not occluding the internal apertures completely (two arrows in <b>F</b>). Scale bars (<b>A</b>) = 10 μm, (<b>B</b>–<b>F</b>) = 1 μm.</p>
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<p><span class="html-italic">Cymbella hustedtii</span>, LM. (<b>A</b>–<b>T</b>). Twenty valves in a series of diminishing size. Scale bar (<b>A</b>–<b>T</b>) = 10 μm.</p>
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<p><span class="html-italic">Cymbella hustedtii</span>, SEM, external view. (<b>A</b>,<b>B</b>). Two frustules; note girdle bands and split locations in girdle view. (<b>C</b>) Valve with valvocopula; note row of poroids along suture (three black arrowheads). (<b>D</b>,<b>E</b>). Two apices; note that connective band surrounds insertion of each apex and that two valvocopulae split near apex (<b>E</b>, two vs; v = valvocopula). Scale bar (<b>A</b>–<b>E</b>) = 5 μm.</p>
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<p><span class="html-italic">Cymbella hustedtii</span>, SEM, external view. (<b>A</b>,<b>B</b>). Two valves; note that the areolae close to the axis are smaller than the other areolae (<b>A</b>, arrows). (<b>C</b>,<b>F</b>). Details showing reniform external openings of areolae and reniform closing plates. Note the struts attached to the areola lumens on either the dorsal or ventral side (arrows and wavy arrows, respectively). (<b>D</b>,<b>E</b>). Two apical details. Note the apical field divided by the distal raphe fissure into two unequal areas: a larger ventral area (LA) and a smaller dorsal area (SA). Scale bars (<b>A</b>,<b>B</b>) = 5 μm, (<b>C</b>–<b>F</b>) = 1 μm.</p>
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<p><span class="html-italic">Cymbella hustedtii</span>, SEM, internal view. (<b>A</b>,<b>E</b>). Two complete valves. (<b>B</b>,<b>F</b>). Middle part details; note that the intermissio is clearly visible (not obscured by a silica hood; two arrows, respectively). (<b>C</b>,<b>D</b>). Two apical details; note the apical field composed of two areas—a larger area (LA) and a smaller area (SA)—and an undulate flap-like silica strip covering the internal apertures of each column of foramina but not occluding the internal apertures completely (two arrows in <b>D</b>). Scale bars (<b>A</b>,<b>E</b>) = 3 μm, (<b>B</b>,<b>F</b>) = 1 μm, (<b>C</b>,<b>D</b>) = 400 nm.</p>
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<p><span class="html-italic">Cymbella juglandis</span>, sp. nov., LM. (<b>A</b>–<b>M</b>). Thirteen valves in a series of diminishing size; note that the ventral margin becomes straighter and straighter in smaller specimens. (<b>A</b>). Illustration of the holotype specimen. Scale bars (<b>A</b>–<b>M</b>) = 10 μm.</p>
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<p><span class="html-italic">Cymbella juglandis</span>, sp. nov., SEM, external view. (<b>A</b>–<b>C</b>). Three valves; note the almost straight raphes and the acute apices. (<b>D</b>–<b>F</b>). Middle part details; note that ca. 2–4 terminal areolae in the dorsal central part have different shapes from the others (wavy arrows) and that ca. 4–7 terminal areolae in the ventral central part also have different shapes from the others (arrows). Scale bars (<b>A</b>–<b>C</b>) = 10 μm, (<b>D</b>–<b>F</b>) = 2 μm.</p>
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<p><span class="html-italic">Cymbella juglandis</span>, sp. nov., SEM, external view. (<b>A</b>–<b>F</b>). Apical details. Note the apical field divided by the distal raphe fissure into two areas: a larger area on the ventral side (LA) and a small area on the dorsal side (SA). Scale bars (<b>A</b>–<b>F</b>) = 1 μm.</p>
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<p><span class="html-italic">Cymbella juglandis</span>, sp. nov., SEM, internal view. (<b>A</b>). A complete valve. (<b>B</b>). Middle part details; note the obscured intermissio (two arrows) and absence of stigmata. (<b>C</b>,<b>D</b>). Apical details; note the apical field divided into two areas—a large area (LA) and a small area (SA)—and an undulate flap-like silica strip above internal apertures of each row of foramina but not occluding the internal apertures completely (two arrows in <b>D</b>). (<b>E</b>). Other middle part details; note the obscured intermissio (two wavy arrows) and absence of stigmata (arrows). (<b>F</b>). Details showing the walnut-kernel-like closing plates (arrows). Scale bars (<b>A</b>) = 4 μm, (<b>B</b>–<b>F</b>) = 1 μm.</p>
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<p><span class="html-italic">Cymbella menyuanensis</span> sp. nov., LM. (<b>A</b>). Initial valve or pre-normal valve; note its vaulted outline. (<b>B</b>–<b>L</b>). Eleven normal vegetative valves in a series of diminishing size. (<b>B</b>). Illustration of the holotype specimen. Scale bar (<b>A</b>–<b>L</b>) = 10 μm.</p>
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<p><span class="html-italic">Cymbella menyuanensis</span> sp. nov., pre-normal valve, SEM, external view. (<b>A</b>). Pre-normal valve. (<b>B</b>–<b>D</b>). Details from (<b>A</b>); note stigmata (arrowheads), various areola openings and orientations (arrows) and poorly developed apical pore fields. Scale bars (<b>A</b>) = 10 μm, (<b>B</b>–<b>D</b>) = 2 μm.</p>
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<p><span class="html-italic">Cymbella menyuanensis</span> sp. nov., SEM, external view. (<b>A</b>). Normal valve. (<b>B</b>). Detail of middle part, note stigmata (arrows). (<b>C</b>,<b>D</b>). Two apical details, note that the distal raphe fissure does not divide the apical pore field into two areas (two arrows). Scale bars (<b>A</b>) = 10 μm, (<b>B</b>–<b>D</b>) = 2 μm.</p>
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<p><span class="html-italic">Cymbella menyuanensis</span> sp. nov., SEM, internal view. (<b>A</b>,<b>C</b>). Two complete valves. (<b>B</b>,<b>D</b>). Details of the middle part; note the stigmata (arrows) and mushroom-shaped closing plates (wavy arrows). (<b>E</b>,<b>F</b>). Two apical details; note that there is an undulate flap-like silica strip above the internal apertures of each row of foramina but not occluding the internal apertures completely (two arrows). Scale bars (<b>A</b>,<b>C</b>) = 10 μm, (<b>B</b>,<b>D</b>–<b>F</b>) = 2 μm.</p>
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<p><span class="html-italic">Cymbella</span> cf. <span class="html-italic">excisiformis</span>, SEM, initial valve. (<b>A</b>). An initial valve. (<b>B</b>). Detail of the middle part; note the irregular central nodule and two proximal raphe endings (two arrows). (<b>C</b>,<b>D</b>). Two apical details; note the perizonium composed of a node (two arrows) and internode (wavy arrow). (<b>E</b>,<b>F</b>). Details showing that the perizonium covers the valve surface before being removed (two arrows). Scale bars (<b>A</b>) = 4 μm, (<b>B</b>–<b>F</b>) = 1 μm.</p>
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<p><span class="html-italic">Cymbella</span> cf. <span class="html-italic">excisiformis</span>, SEM, details of perizonium. (<b>A</b>–<b>D</b>). The structures of the perizonium, which is composed of two parts: the nodes and the internodes (labeled in <b>A</b>). The internode is also composed of two parts: strips and openings between them (labelled in <b>D</b>). Scale bars (<b>A</b>–<b>C</b>) = 1 μm, (<b>D</b>) = 400 nm.</p>
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<p><span class="html-italic">Cymbella menyuanensis</span> sp. nov., SEM, initial frustule. (<b>A</b>). An initial frustule. (<b>B</b>). Detail of the middle part; note the rectangle to oblong external openings of areolae and two girdle bands (two arrows). (<b>C</b>,<b>D</b>). Two apical details; note that the perizonium encloses the entire frustule, the rectangle to oblong external openings of areolae (white arrow) and irregular apical pore field (black arrow). (<b>E</b>,<b>F</b>). Details showing that the perizonium covers the valve surface and irregular apical pore field (one black arrow). Scale bars (<b>A</b>) = 10 μm, (<b>B</b>–<b>E</b>) = 3 μm, (<b>D</b>,<b>F</b>) = 1 μm.</p>
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<p><span class="html-italic">Cymbella menyuanensis</span> sp. nov., SEM, details of perizonium. (<b>A</b>,<b>B</b>). Details showing that the perizonium encloses the entire frustule (three arrows). (<b>C</b>). Detail showing that the perizonium is composed of two parts: the nodes and the internodes. The internode is also composed of two parts: strips and openings between them. Scale bars (<b>A</b>–<b>C</b>) = 3 μm.</p>
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<p>Areolae and their occlusions in five <span class="html-italic">Cymbella</span> species. (<b>A</b>,<b>B</b>). Shapes and sizes of external (<b>A</b>) and internal (<b>B</b>) openings and occlusions in <span class="html-italic">C. apiculatophora</span>. (<b>C</b>,<b>D</b>). Shapes and sizes of external (<b>C</b>) and internal (<b>D</b>) openings and occlusions in <span class="html-italic">C. hunanensis</span>. (<b>E</b>,<b>F</b>). Shapes and sizes of external (<b>E</b>) and internal (<b>F</b>) openings and occlusions in <span class="html-italic">C. hustedtii</span>. (<b>G</b>,<b>H</b>). Shapes and sizes of external (<b>G</b>) and internal (<b>H</b>) openings and occlusions in <span class="html-italic">C. menyuanensis</span>. (<b>I</b>,<b>J</b>). Shapes and sizes of external (<b>I</b>) and internal (<b>J</b>) openings and occlusions in <span class="html-italic">C. juglandis</span>.</p>
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18 pages, 5830 KiB  
Article
Effect of Paleoenvironmental Conditions on the Distribution of Lower Carboniferous Shale in Yaziluo Rift Trough, South China: Insights from Major/Trace Elements and Shale Composition
by Xianglin Chen, Qiuchen Xu, Yinglun Qin, Rong Chen, Yufang Wang, Dishi Shi, Jing Bai, Kun Yuan, Wenpan Cen, Fei Li and Tuo Lin
Minerals 2024, 14(7), 659; https://doi.org/10.3390/min14070659 - 26 Jun 2024
Viewed by 987
Abstract
Paleoenvironmental conditions significantly influence the distribution patterns and organic matter enrichment of shale. This study investigated the vertical variations of major elements, trace elements, and total organic carbon (TOC) in the Lower Carboniferous marine shale from the Yaziluo Rift Trough, South China, to [...] Read more.
Paleoenvironmental conditions significantly influence the distribution patterns and organic matter enrichment of shale. This study investigated the vertical variations of major elements, trace elements, and total organic carbon (TOC) in the Lower Carboniferous marine shale from the Yaziluo Rift Trough, South China, to understand the paleoenvironmental conditions, including redox conditions, terrigenous detrital input, paleoproductivity, and paleo-seawater depth. The Lower Carboniferous formation consists of three sedimentary facies: basin facies, lower slope facies, and upper slope facies. From the basin to the lower slope and then to the upper slope facies, TOC, quartz, and pyrite contents gradually decrease, whereas the carbonate mineral content shows an increasing trend. A continuous decline in paleo-seawater depth transformed a deep-water anoxic environment with high paleoproductivity and low detrital input in the basin facies into a semi-deep-water environment with dysoxic-oxic conditions and moderate detrital influx in the lower slope facies, evolving further into a suboxic environment with high detrital flux in the upper slope facies. The geochemistry results suggest that anoxic conditions and high paleoproductivity were the primary controls on organic matter enrichment in the siliceous shale of the basin facies. In contrast, redox conditions significantly influenced organic matter accumulation in the mixed shale of the lower slope facies, attributed to relatively low paleoproductivity in a more restricted marine setting. Additionally, the adsorption of carbon components by clay minerals facilitated the preservation of organic matter in the calcareous shale of the upper slope facies. Full article
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Figure 1
<p>(<b>A</b>) Distribution of the Yaziluo Rift Trough during the late Carboniferous period, showing the sampling wells (Well A, Well B and Well C); (<b>B</b>) sequence stratigraphic framework according to Geology and Mineral Resources Bureau of Guangxi Zhuang Autonomous Region, 1985 [<a href="#B17-minerals-14-00659" class="html-bibr">17</a>].</p>
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<p>Ternary diagram showing the mineralogy of the three major lithofacies of Lower Carboniferous shale in the Yaziluo Rift Trough (modified from Ma et al. [<a href="#B2-minerals-14-00659" class="html-bibr">2</a>], the Cms, Ms, Cs, and Ss represent argillaceous shale lithofacies, mixed shale lithofacies, carboniferous shale lithofacies, and siliceous shale lithofacies, respectively).</p>
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<p>Covariation of Mo<sub>EF</sub> and U<sub>EF</sub> from the Lower Carboniferous shale (modified from Algeo and Tribovillard (2009) [<a href="#B21-minerals-14-00659" class="html-bibr">21</a>]), exhibiting water-mass restriction and redox conditions.</p>
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<p>Stratigraphic distributions of redox (V/Cr and U/Th), paleo-seawater depth (Co/Ti and Sr/Ba), detrital influx (Al and Ti), and paleoproductivity (P/Ti and Ba/Al) proxies in Well A, respectively.</p>
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<p>Stratigraphic distributions of redox (V/Cr and U/Th), paleo-seawater depth (Co/Ti and Sr/Ba), detrital influx (Al and Ti), and paleoproductivity (P/Ti and Ba/Al) proxies in Well B, respectively.</p>
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<p>Stratigraphic distributions of redox (V/Cr and U/Th), paleo-seawater depth (Co/Ti and Sr/Ba), detrital influx (Al and Ti), and paleoproductivity (P/Ti and Ba/Al) proxies in Well C, respectively.</p>
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<p>Correlation between redox proxies and TOC in the Lower Carboniferous formation. (<b>A</b>) V/Cr and TOC; (<b>B</b>) U/Th and TOC.</p>
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<p>Correlation between paleoproductivity proxies and TOC in the Lower Carboniferous formation. (<b>A</b>) Ba/Al and TOC; (<b>B</b>) P/Ti and TOC.</p>
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<p>Correlation between detrital proxies and TOC in the Lower Carboniferous formation. (<b>A</b>) Al and TOC; (<b>B</b>) Ti and TOC.</p>
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<p>Sedimentary model of the Lower Carboniferous formation. The location of well and variations in paleoenvironment proxies and shale components are schematic.</p>
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15 pages, 2427 KiB  
Article
Iron Composition of a Typical Loess-Paleosol Sequence in Northeast China
by Zhong-Xiu Sun, Si-Wei Liu and Ying-Ying Jiang
Agronomy 2024, 14(6), 1333; https://doi.org/10.3390/agronomy14061333 - 20 Jun 2024
Viewed by 564
Abstract
Iron isotope compositions, along with the partial extraction of iron in its various forms, can be utilized to investigate the complex interplay of iron migration and transformation with respect to iron isotope patterns. This study investigated the iron composition of a typical loess-paleosol [...] Read more.
Iron isotope compositions, along with the partial extraction of iron in its various forms, can be utilized to investigate the complex interplay of iron migration and transformation with respect to iron isotope patterns. This study investigated the iron composition of a typical loess-paleosol sequence in Northeast China and aimed to understand the influence of iron migration and transformation of the typical loess-paleosol sequence on iron isotopes and environmental and climatic changes that occurred in the region over time by analyzing the distribution and characteristics of iron compositions in sedimentary layers. Samples were collected from Chaoyang in Northeast China, and the iron isotopic composition was analyzed using the multi-receiver inductively coupled plasma mass spectrometer (MC-ICP-MS). The findings revealed depth-dependent variations in the content of different iron forms, reflecting paleoclimatic shifts primarily through pedogenic transformation processes. Notably, iron migration within the section was observed to be limited. The variations in the reddening index and magnetic susceptibility of the loess-paleosol were primarily influenced by the presence of free iron (Fed), exhibiting a range of colors from yellow to red-yellow and red. The δ56Fe values for loess and paleosols ranged from 0.097 ± 0.035‰ to 0.167 ± 0.010‰, with an average of 0.133 ± 0.024‰ and a coefficient of variation (CV) of 15.66% at the stratum scale. These values indicated a systematic enrichment of heavy iron isotopes and a significant negative correlation with the slightly fluctuating total iron content. Specifically, our analysis highlighted distinct differences in δ56Fe values between paleosol (0.126 ± 0.024‰) and loess (0.146 ± 0.021‰). The δ56Fe in Fed was negative, averaging −0.101 ± 0.022‰, while the δ56Fe in silicate-bound iron was positive, averaging 0.156 ± 0.032‰. Intense pedogenesis, driven by warm and wet climates, facilitated iron transformations and migrations, resulting in the accumulation of light iron isotopes in the paleosols. These transformations and migrations were predominantly observed in microdomains characterized by iron depletions and concentrations, as reflected in the profile morphologies. However, the limited iron transformations and migrations did not result in significant Fe redistribution within the soil section, as evidenced by the limited variations in δ56Fe with soil depth at the stratum scale. Sampling from the stratum or pedogenic horizon could potentially create the illusion of the minimal fractionation of iron isotopes within the sequence. Therefore, a detailed examination of the iron isotope composition in the micro-domains of the loess-paleosol sequence is crucial to elucidate the fractionation processes and mechanisms of iron isotopes during the formation of these sequences. Full article
(This article belongs to the Special Issue Soil Evolution, Management, and Sustainable Utilization)
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<p>(<b>A</b>) A schematic map presenting the location of the Chaoyang section. The inset map shows the location of Chaoyang in China. The schematic map was plotted based on the base map of the World Imagery Wayback (<a href="https://livingatlas.arcgis.com/wayback/" target="_blank">https://livingatlas.arcgis.com/wayback/</a>) using Arc GIS 10.2.2. (<b>B</b>) Landscape photo of the Chaoyang section. Photos (<b>C</b>) and schematic (<b>D</b>) of the Chaoyang section showing boundaries based on age and morphological descriptions [<a href="#B4-agronomy-14-01333" class="html-bibr">4</a>]. L indicates loess, and S indicates paleosol. Note: S0 represents modern soil. The upper (0–195 cm), middle (195–228 cm), and lower parts (228–1985 cm) of the observed section are abbreviated as UPP, MIP, and LOP, respectively.</p>
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<p>Comparisons of δ<sup>56</sup>Fe, various forms of iron content, and their ratios with soil depth in the typical loess-paleosol sequence of Northeast China.</p>
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<p>Comparative analysis of iron content curves in various forms alongside magnetic susceptibility and redness rating index (RR) with respect to depth.</p>
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<p>Characteristics of the migration/accumulation of δ<sup>56</sup>Fe and Fet with respect to soil depth in the typical loess-paleosol sequence.</p>
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11 pages, 1954 KiB  
Article
Sulfur Isotope Characteristics in the Qian-34 Section of the Qianjiang Depression and Its Implications for the Paleoenvironment
by Tianyu Wang, Ren Wei, Kun Ling and Lin Dong
Minerals 2024, 14(6), 626; https://doi.org/10.3390/min14060626 - 20 Jun 2024
Viewed by 634
Abstract
Pyrite is an important proxy used to reflect the redox state of a sedimentary environment. Currently available studies on pyrite focus on the process of sulfur cycles between an ocean and sediment. However, our understanding of the biogeochemical cycle of sulfur in terrestrial [...] Read more.
Pyrite is an important proxy used to reflect the redox state of a sedimentary environment. Currently available studies on pyrite focus on the process of sulfur cycles between an ocean and sediment. However, our understanding of the biogeochemical cycle of sulfur in terrestrial lake basins remains unclear, and the growth patterns of different types of pyrite are poorly understood. In this paper, we used samples from the 34 section of the Qianjiang depression in the Jianghan Basin as direct research objects by combining pyrite and sulfur isotope determination. The one-dimensional diffusion–advection–reaction simulation (1D-DAR) model was applied to simulate the changes in the pyrite content and sulfur isotope values in the sediment. The results show that the sediments in the saline lake basin environment contain a high organic matter content, a high sedimentation rate, and a high H2S diffusion oxidation rate, reflecting the strong reducing background and high productivity of this ancient lake. Sensitivity tests revealed that the organic matter content and H2S diffusion oxidation rate at the sediment–water interface are sensitive to the pyrite content. The sedimentation rate, organic matter content, and sulfate concentration are sensitive to the pyrite’s sulfur isotope values. However, the variation in the active iron content had little effect on the pyrite content or sulfur isotope value. Full article
(This article belongs to the Special Issue Sulfide Mineralogy and Geochemistry)
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<p>Geological setting and stratigraphic column of the Qianjiang depression, Jianghan Basin. (<b>a</b>) The location of the Qianjiang depression, Jianghan Basin (modified from Huang et al., 2014 and Fang et al., 2014 [<a href="#B27-minerals-14-00626" class="html-bibr">27</a>,<a href="#B28-minerals-14-00626" class="html-bibr">28</a>]) and (<b>b</b>) sedimentary lithofacies of the Eocene Qianjiang Formation in the Qianjiang Depression (modified from Huang et al., 2014 and Wei et al., 2023 [<a href="#B27-minerals-14-00626" class="html-bibr">27</a>,<a href="#B32-minerals-14-00626" class="html-bibr">32</a>]).</p>
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<p>Geochemical histogram of the Qian 3<sup>4</sup> section of the BX7 well in the Qianjiang depression (TOC data are from Wei et al., 2023 [<a href="#B32-minerals-14-00626" class="html-bibr">32</a>]). The evaporites are mainly anhydrite and glauberite.</p>
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<p>Model structure of 1D-DAR simulation (SWI: sediment–water interface) (modified from Lang et al., 2020 [<a href="#B11-minerals-14-00626" class="html-bibr">11</a>]).</p>
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<p>The 1D-DAR model results of pyrite’s sulfur isotope values. (<b>a</b>) The sedimentation rate of siliciclastic-dominated mixed sedimentary rocks is lower than that of carbonate-dominated mixed sedimentary rocks, and the organic matter abundance of siliciclastic-dominated mixed sedimentary rocks is higher than that of carbonate-dominated mixed sedimentary rocks; (<b>b</b>) The proportion of H<sub>2</sub>S oxidized at the sediment–water interface of siliciclastic-dominated mixed sedimentary rocks is higher than that of carbonate-dominated mixed sedimentary rocks.</p>
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<p>Sulfur isotope model sensitivity test.</p>
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<p>Trends of different variables in the sulfur isotope model.</p>
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