Abstract:a b s t r a c t a r t i c l e i n f oThe site complex Ounjougou on the Dogon Plateau (Mali) comprises sediments up to 100,000 years old with numerous Pleistocene and Holocene sequences. The site Ravin de la Mouche (11.4-10.2 ka) is of special archaeological significance because in its Early Holocene deposits, pottery sherds have been found which are among the oldest in Africa. For a better understanding of the environmental conditions which might have contributed to the innovation of pottery making, a multi-pr… Show more
“…Because phytoliths are normally well preserved in oxidizing environments, their morphological assemblages have been widely used for paleo-environmental reconstructions and archaeological and paleontological research (e.g., Piperno and Becker, 1996;Alexandre et al, 1999;Prebble et al, 2002;Prasad et al, 2005;Bremond et al, 2005Bremond et al, , 2008aPiperno, 2006;Alam et al, 2009;Neumann et al, 2009;Rossouw et al, 2009). In parallel, quantification of phytoliths in plants, soils, and rivers has been used to study the biogeochemical cycle of silica, which itself is coupled to the global C cycle (Blecker et al, 2006;Struyf et al, 2009;Cornelis et al, 2011;Alexandre et al, 2011).…”
Abstract. Plants absorb and transport silicon (Si) from soil, and precipitation of Si within the living plants results in micrometric amorphous biosilica particles known as phytoliths. During phytolith formation, a small amount of carbon (<2 %) can become occluded in the silica structure (phytC) and therefore protected from degradation by the environment after plant tissue decomposition. Since the major C source within plants is from atmospheric carbon dioxide (CO 2 ) via photosynthesis, the current understanding is that the radiocarbon ( 14 C) content of phytC should reflect the 14 C content of atmospheric CO 2 at the time the plant is growing. This assumption was recently challenged by 14 C data from phytoliths extracted from living grasses that yielded ages of several thousand years (2-8 kyr BP; in radiocarbon years "Before Present" (BP), "Present" being defined as 1950). Because plants can take up small amounts of C of varying ages from soils (e.g., during nutrient acquisition), we hypothesized that this transported C within the plant tissue could be attached to or even embedded in phytoliths. In this work, we explore this hypothesis by reviewing previously published data on biosilica mineralization and plant nutrient acquisition as well as by evaluating the efficiency of phytolith extraction protocols from scanning electron microscope (SEM) images and energy dispersive spectrometer (EDS) analyses from harvested grasses phytolith concentrates. We show that current extraction protocols are inefficient since they do not entirely remove recalcitrant forms of C from plant tissue. Consequently, material previously measured as "phytC" may contain at least some fraction of soil-derived C (likely radiocarbon-old) taken up by roots. We also suggest a novel interpretation for at least some of the phytC -which enters via the root pathway during nutrient acquisition -that may help to explain the old ages previously obtained from phytolith concentrates.
“…Because phytoliths are normally well preserved in oxidizing environments, their morphological assemblages have been widely used for paleo-environmental reconstructions and archaeological and paleontological research (e.g., Piperno and Becker, 1996;Alexandre et al, 1999;Prebble et al, 2002;Prasad et al, 2005;Bremond et al, 2005Bremond et al, , 2008aPiperno, 2006;Alam et al, 2009;Neumann et al, 2009;Rossouw et al, 2009). In parallel, quantification of phytoliths in plants, soils, and rivers has been used to study the biogeochemical cycle of silica, which itself is coupled to the global C cycle (Blecker et al, 2006;Struyf et al, 2009;Cornelis et al, 2011;Alexandre et al, 2011).…”
Abstract. Plants absorb and transport silicon (Si) from soil, and precipitation of Si within the living plants results in micrometric amorphous biosilica particles known as phytoliths. During phytolith formation, a small amount of carbon (<2 %) can become occluded in the silica structure (phytC) and therefore protected from degradation by the environment after plant tissue decomposition. Since the major C source within plants is from atmospheric carbon dioxide (CO 2 ) via photosynthesis, the current understanding is that the radiocarbon ( 14 C) content of phytC should reflect the 14 C content of atmospheric CO 2 at the time the plant is growing. This assumption was recently challenged by 14 C data from phytoliths extracted from living grasses that yielded ages of several thousand years (2-8 kyr BP; in radiocarbon years "Before Present" (BP), "Present" being defined as 1950). Because plants can take up small amounts of C of varying ages from soils (e.g., during nutrient acquisition), we hypothesized that this transported C within the plant tissue could be attached to or even embedded in phytoliths. In this work, we explore this hypothesis by reviewing previously published data on biosilica mineralization and plant nutrient acquisition as well as by evaluating the efficiency of phytolith extraction protocols from scanning electron microscope (SEM) images and energy dispersive spectrometer (EDS) analyses from harvested grasses phytolith concentrates. We show that current extraction protocols are inefficient since they do not entirely remove recalcitrant forms of C from plant tissue. Consequently, material previously measured as "phytC" may contain at least some fraction of soil-derived C (likely radiocarbon-old) taken up by roots. We also suggest a novel interpretation for at least some of the phytC -which enters via the root pathway during nutrient acquisition -that may help to explain the old ages previously obtained from phytolith concentrates.
“…Phytoliths are good indicators to trace the existence of true tropical forest environments in tropical Africa (Fig. 4) (Bremond et al, 2005a;Aleman et al, 2011) but, conversely, they still fail to reconstruct the ligneous cover in tropical savanna environments (Neumann et al, 2009;Novello et al, 2012). As a result, the Bol phytolith data cannot provide much information on the presence/abundance of the ligneous cover in these paleo-savannas.…”
Section: Tropical Savanna As the Dominant Biome In The Basinmentioning
confidence: 99%
“…9) currently occurring in the Lake Chad basin (Gaston, 1996). Some authors (Neumann et al, 2009;Prasad et al, 2011), however, asserted to have identified a specific bilobate type -"the bilobate type with scoped ends" -which they described as diagnostic of the Ehrhartoideae grass subfamily. The description criteria and classification used in this study were not designed to specifically isolate this bilobate type that may have thus be counted as part of the bilobate types with notched ends (Bi8 type) (see Table 3 for Bi-8 type photograph), which in fact probably include a larger morphological variability than the bilobate type with scoped ends itself.…”
Section: Lesson For the Pliocene Grass Expansion In Central Africamentioning
A discontinuous 200 m-long borehole drilled in the Bol Archipelago (13°N, Lake Chad) provided 25 samples, which were dated using the 10 Be/ 9 Be method and analyzed for their micro-biological content. The dating provided ages ranging from 6.3 ± 0.1 to 2.6 ± 0.1 Ma, a period contemporaneous with the Pliocene fossil localities located in the current Djurab desert of Chad (16-17°N). Well-preserved diatom assemblages first occurred at 4.7 ± 0.1 Ma and were dominated by the freshwater planktonic genera Aulacoseira and Stephanodiscus until the end of the Pliocene. This supports the recurrence of lacustrine conditions at Bol during all the Pliocene. The presence of pelite and argillaceous deposits in the core before 4.7 ± 0.1 Ma, however, suggests that the lake settled earlier, at least since 6.3 ± 0.1 Ma. The abundance of Afromontane pollen taxa at 4.2 ± 0.1 Ma and the occurrence of trapeziform polylobate phytoliths throughout the sequence suggest significant vegetation inputs from the southern highlands, while the importance of kaolinite in the clay sediments indicates a water supply predominantly from the south during the Pliocene. Phytolith assemblages are all dominated by lobate grass silica short cells and by blocky and elongate types, which attest to the presence of herbaceous-dominated vegetation around Bol and/or in the southern drainage basin during the Pliocene. This result is also supported by the pollen assemblage described at 4.2 ± 0.1 Ma, which shows highest affinity for the savanna biome. Moreover, low values for the Xerophytic grass phytolith index indicate the presence of humid-loving (mesophytic and aquatic) grass communities in this vegetation. At last, significant variations in the abundance of blocky and elongate phytoliths are indicative of local alternations of fully lacustrine and marshy conditions at Bol. Particularly between 3.6 and 2.7 Ma, the abundance of silicified bulliform cells combined with the absence of diatoms support a significant lacustrine reduction at Bol favoring the increasing of local marshy vegetation.
“…The rainy season contributed to rambling flow with strong competence in a wide sandy gravel bed while the dry season led to decantation deposits in permanent pools as shown by the absence of desiccation evidence at the top of the fine deposits attributable to the dry season. Moreover, for the first time in the sedimentation, the abundance and nature of organic material evidences the importance of the vegetal cover in the valley base (riverain) and slopes (Eichhorn and Neumann, 2007;Neumann et al, 2009). This indicates the transition to a calmer river system that can be explained by the reconquest of vegetation on the slopes and in the base of the valley, limiting the sedimentary contribution to the talweg.…”
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