Boron isotope values in Paleozoic brachiopods and corals, collected from the Yunnan-Guizhou Plateau, China, can be used to constrain the boron isotope compositions of past oceans. All brachiopod shells and coral samples were screened for diagenetic recrystallization by cathodoluminescence microscopy, trace element geochemistry of B, Fe, Mn, Sr, and scanning electron microscopy. The boron isotope ratios for brachiopods in Silurian, Devonian, Carboniferous, and Triassic calcites are in the ranges 8.9‰-14.0‰, 8.8‰-13.8‰, 10.3‰-16.3‰, and 6.7‰-12.4‰, respectively. The boron isotope ratios of coral calcites in the Silurian, Devonian, and Permian are 9.1‰-12.2‰, 6.1‰-13.8‰, and 9.2‰-16.1‰, respectively. The δ 11 B values for both brachiopods and corals are significantly lower than those for modern biogenic carbonates, indicating that the Paleozoic oceans were depleted of δ 11 B by up to 10‰. Our results are consistent with previous published studies. The boron isotope compositions of corals and brachiopods show the consistent trends. The low δ 11 B values may be explained by an enhanced riverine flux of boron from the continents. boron isotope, coral, brachiopod, Paleozoic Citation: Ma Y Q, Xiao Y K, He M Y, et al. Boron isotopic composition of Paleozoic brachiopod and coeval coral calcites in Yunnan-Marine carbonate chemistry and atmospheric concentrations of the greenhouse gas CO 2 are tightly coupled, so the reconstruction of atmospheric PCO 2 from marine carbonate minerals is an important goal for paleoclimatology. One of the most promising carbonate chemistry proxies for the marine environment is the boron isotopic composition ( 11 B) of biogenic calcium carbonate, which is an established tracer for paleo-pH [1][2][3][4][5]. Boron dissolved in seawater occurs as B(OH) 4 -and B(OH) 3 , and the relative proportion of these species is determined by the pH of the ambient seawater. The boron isotopic composition of the two species exhibits a significant fractionation, with B(OH) 4 -depleted in 11 B by ~19‰ with respect to B(OH) 3 (=1.0194) [6]. More recent studies suggest a larger fractionation factor both on the basis of theoretical considerations (=1.027) [7] and in direct measurements (=1.0272) [8]. If seawater pH changes, the relative proportion of the two species and the isotopic compositions of B(OH) 4 -and B(OH) 3 also change. Because it has been generally assumed that the charged species B(OH) 4 -is incorporated into carbonate minerals without any significant boron isotopic fractionation [1, 4], the 11 B of biogenic carbonates has been used as a paleo-pH proxy [2, 5,