Wilkinson Adam D, Collier Catherine J, Flores Florita, Mercurio Phil, O'Brien Jake, Ralph Peter J, Negri Andrew P
College of Marine and Environmental Sciences, James Cook University, Townsville, Queensland, Australia; Australian Institute of Marine Science, Townsville, Queensland, Australia.
College of Marine and Environmental Sciences, James Cook University, Townsville, Queensland, Australia; Centre for Tropical Water & Aquatic Ecosystem Research (TropWATER), James Cook University, Cairns, Queensland, Australia.
PLoS One. 2015 Feb 12;10(2):e0117541. doi: 10.1371/journal.pone.0117541. eCollection 2015.
Photosystem II (PSII) herbicides have been detected in nearshore tropical waters such as those of the Great Barrier Reef and may add to the pressure posed by runoff containing sediments and nutrients to threatened seagrass habitats. There is a growing number of studies into the potential effects of herbicides on seagrass, generally using large experimental setups with potted plants. Here we describe the successful development of an acute 12-well plate phytotoxicity assay for the PSII herbicide Diuron using isolated Halophila ovalis leaves. Fluorescence images demonstrated Diuron affected the entire leaf surface evenly and responses were not influenced by isolating leaves from the plant. The optimum exposure duration was 24 h, by which time the inhibition of effective quantum yield of PSII (∆F/F(m)') was highest and no deterioration of photosystems was evident in control leaves. The inhibition of ∆F/F(m)' by Diuron in isolated H. ovalis leaves was identical to both potted and hydroponically grown plants (with leaves remaining attached to rhizomes), indicating similar reductions in photosynthetic activity in these acute well-plate assays. The sensitivity of the assay was not influenced by irradiance (range tested 40 to 400 μmol photons m(-2) s(-1)). High irradiance, however, caused photo-oxidative stress in H. ovalis and this generally impacted in an additive or sub-additive way with Diuron to damage PSII. The bioassay using isolated leaves is more rapid, uses far less biological material and does not rely on specialised aquarium facilities in comparison with assays using potted plants. The development and validation of this sensitive bioassay will be useful to reliably screen and monitor the phytotoxicity of existing and emerging PSII herbicides and contribute to risk assessments and water quality guideline development in the future.
在大堡礁等近岸热带水域已检测到光系统II(PSII)除草剂,这可能会增加含有沉积物和养分的径流对受威胁海草栖息地造成的压力。目前有越来越多关于除草剂对海草潜在影响的研究,这些研究通常使用盆栽植物进行大型实验设置。在此,我们描述了一种使用分离出的卵叶喜盐草叶片针对PSII除草剂敌草隆的急性12孔板植物毒性测定法的成功开发。荧光图像显示敌草隆均匀地影响了整个叶片表面,并且响应不受从植株上分离叶片的影响。最佳暴露时间为24小时,此时PSII有效量子产率(∆F/F(m)')的抑制率最高,且对照叶片中光系统未出现明显退化。在分离出的卵叶喜盐草叶片中,敌草隆对∆F/F(m)'的抑制作用与盆栽植物和水培植物(叶片仍附着于根茎)相同,这表明在这些急性孔板测定中光合活性有类似程度的降低。该测定法的灵敏度不受辐照度(测试范围为40至400 μmol光子 m(-2) s(-1))的影响。然而,高辐照度会在卵叶喜盐草中引起光氧化应激,这通常与敌草隆以累加或次累加的方式共同作用,损害PSII。与使用盆栽植物的测定法相比,使用分离叶片的生物测定法速度更快,使用的生物材料少得多,并且不依赖专门的水族箱设施。这种灵敏生物测定法的开发和验证将有助于可靠地筛选和监测现有及新出现的PSII除草剂对植物的毒性,并为未来的风险评估和水质准则制定做出贡献。