Lisle John T, Robbins Lisa L
U. S. Geological Survey, St. Petersburg Coastal and Marine Science Center St. Petersburg, FL, USA.
Front Microbiol. 2016 Dec 9;7:1958. doi: 10.3389/fmicb.2016.01958. eCollection 2016.
Removal of carbon through the precipitation and burial of calcium carbonate in marine sediments constitutes over 70% of the total carbon on Earth and is partitioned between coastal and pelagic zones. The precipitation of authigenic calcium carbonate in seawater, however, has been hotly debated because despite being in a supersaturated state, there is an absence of persistent precipitation. One of the explanations for this paradox is the geochemical conditions in seawater cannot overcome the activation energy barrier for the first step in any precipitation reaction; nucleation. Here we show that virally induced rupturing of photosynthetic cyanobacterial cells releases cytoplasmic-associated bicarbonate at concentrations ~23-fold greater than in the surrounding seawater, thereby shifting the carbonate chemistry toward the homogenous nucleation of one or more of the calcium carbonate polymorphs. Using geochemical reaction energetics, we show the saturation states (Ω) in typical seawater for calcite (Ω = 4.3), aragonite (Ω = 3.1), and vaterite (Ω = 1.2) are significantly elevated following the release and diffusion of the cytoplasmic bicarbonate (Ω = 95.7; Ω = 68.5; Ω = 25.9). These increases in Ω significantly reduce the activation energy for nuclei formation thresholds for all three polymorphs, but only vaterite nucleation is energetically favored. In the post-lysis seawater, vaterite's nuclei formation activation energy is significantly reduced from 1.85 × 10 J to 3.85 × 10 J, which increases the nuclei formation rate from highly improbable (<<1.0 nuclei cm s) to instantaneous (8.60 × 10 nuclei cm s). The proposed model for homogenous nucleation of calcium carbonate in seawater describes a mechanism through which the initial step in the production of carbonate sediments may proceed. It also presents an additional role of photosynthesizing microbes and their viruses in marine carbon cycles and reveals these microorganisms are a collective repository for concentrated and reactive dissolved inorganic carbon (DIC) that is currently not accounted for in global carbon budgets and carbonate sediment diagenesis models.
通过海洋沉积物中碳酸钙的沉淀和埋藏来去除碳,占地球总碳量的70%以上,并且在沿海和远洋区域之间分配。然而,海水中自生碳酸钙的沉淀一直备受争议,因为尽管处于过饱和状态,但却没有持续的沉淀。对于这一矛盾的一种解释是,海水中的地球化学条件无法克服任何沉淀反应第一步(成核)的活化能障碍。在这里,我们表明,病毒诱导光合蓝细菌细胞破裂会释放出与细胞质相关的碳酸氢盐,其浓度比周围海水高约23倍,从而使碳酸盐化学朝着一种或多种碳酸钙多晶型物的均匀成核方向转变。利用地球化学反应能量学,我们表明,在细胞质碳酸氢盐释放和扩散后,典型海水中方解石(Ω = 4.3)、文石(Ω = 3.1)和球霰石(Ω = 1.2)的饱和状态(Ω)显著升高(Ω = 95.7;Ω = 68.5;Ω = 25.9)。这些Ω的增加显著降低了所有三种多晶型物的核形成阈值的活化能,但只有球霰石的成核在能量上是有利的。在裂解后的海水中,球霰石细胞核形成的活化能从1.85×10焦耳显著降低到3.85×10焦耳,这使得细胞核形成速率从极不可能(<<1.0个核厘米秒)增加到瞬间(8.60×10个核厘米秒)。所提出的海水中碳酸钙均匀成核模型描述了碳酸盐沉积物产生的初始步骤可能进行的一种机制。它还揭示了光合微生物及其病毒在海洋碳循环中的额外作用,并表明这些微生物是浓缩和活性溶解无机碳(DIC)的集体储存库,目前在全球碳预算和碳酸盐沉积物成岩模型中并未考虑到这些碳。