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Biogenic volatile organic compounds (BVOCs) emitted by tropical plants represent a significant proportion of global emissions, but the in-situ BVOC measurements in tropical rainforests are extremely sparse. Herein, a vehicle-mounted mobile monitoring system was developed for in-situ online investigations of BVOC emissions from thirty representative tree species in the tropical rainforests of Hainan Island, southern China. The results showed that monoterpenes were the primary BVOCs emitted from most broadleaf trees. Isoprene, sabinene, γ-terpinene and β-ocimene were the most abundant BVOCs. Localized canopy-scale emission factors (EFs) exhibited notable discrepancies with the defaults in the Model of Emissions of Gases and Aerosols from Nature (MEGAN), specifically with isoprene EFs being slightly lower than the model, while the EFs for monoterpenes and sesquiterpenes were 1 to 27 times higher than those in MEGAN. The BVOC emission inventory for the predominant mature forest species in Hainan Island in 2023 was further estimated to be 244.43 Gg C·yr -1 , with isoprene and monoterpenes accounting for 74 % and 16 %, respectively. Additionally, unimodal monthly variation patterns were revealed, with BVOC emissions peaked in July (30.08 Gg C·yr -1 ) and bottomed in January (8.84 Gg C·yr -1 ). This study demonstrates the potential and versatility of the applied mobile platform for in-situ online measurements of plant volatiles. Our findings provide important data support for reducing uncertainties in BVOC emission estimations in tropical rainforests and for evaluating their health benefits in the context of forest therapy., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024. Published by Elsevier B.V.)

Two acylhydrazone based zinc(II) complexes [Zn(HL) 2 Cl 2 (CH 3 OH) 2 ] (Zn1) and [ZnL(AC)] 2 (Zn2) were synthesized from 3-(1-(salicyloylhydrazono)ethyl) pyridine (HL). Single crystal X-ray structure analyses showed that complexes Zn1 and Zn2 have a zero-dimensional monomer or dimer structure. Antiproliferative activity studies revealed that Zn1 and Zn2 are both more effective against A549 cells than cisplatin. The results of the reactive oxygen species (ROS) generation assay on A549 cells showed that both Zn1 and Zn2 induced apoptosis through ROS accumulation. The apoptosis-inducing and cell cycle arrest effects of Zn1 and Zn2 on A549 cells indicated that the antitumor effect was achieved through apoptosis induction and inhibition of DNA synthesis by blocking the G 0 /G1 phase of the cell cycle. What's more, the results of wound-healing assay showed that Zn1 and Zn2 could inhibit the migration of A549 cells. Western blot analysis further demonstrated that Zn1 and Zn2 induced cell apoptosis through the mitochondrial pathway, in which process, the expression level of cytochrome C, cleaved-PARP, cleaved-caspase 3 and cleaved-caspase 9 proteins increased while pro-caspase 3 and pro-caspase 9 expression decreased. In vivo anticancer evaluation demonstrated that both Zn1 and Zn2 complexes effectively inhibited tumor growth without causing significant toxicity in systemic organs., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024. Published by Elsevier Inc.)