2. 中国科学院大学, 北京 100049
2. University of Chinese Academy of Sciences, Beijing 100049, China
三峡水库为达到“蓄清排浊”目的, 采用春夏排水和秋冬蓄水的运行调度方式, 导致在库区高程145~175 m之间形成与天然河流涨落季节相反, 面积约349 km2的消落带(water-level fluctuation zone, WLFZ)[1].库区消落带反复经历“淹水-落干”循环, 消落带土壤处于反复的干湿交替变化之中, 强烈的物理、化学和生物等过程交替发生, 导致突出的土壤结构变化[2]、有机质分解矿化[3]、离子迁移转化[4]和微生物群落转变[5]等问题, 显著影响磷的生物地球化学循环.土壤磷主要分为无机磷和有机磷, 因其本底、形态结构和生物有效性的不同, 各形态磷在水-土界面的迁移转化过程差异显著[6], 对上覆水磷污染负荷的贡献也有较大区别[7, 8].因此, 研究消落带土壤磷形态赋存特征对于了解磷释放风险具有重要意义.
三峡水库运行以后, 支流流速减缓, 水体自净能力下降.同时, 陆地向水体输入的营养元素显著增加, 易在支流库湾处累积, 加上适宜的温度, 使得支流库湾“水华”现象频发[9, 10].目前, 针对库区水体富营养化问题, 从控源角度出发, 除了关于库区水质时空分布特征[11, 12]、营养物质来源解析[13]、沉积物各形态磷生物有效性[14, 15]、吸附-释放性能[16]和迁移转化规律研究[7, 17]以外, 有关消落带土壤磷释放的研究主要集中在降雨时期不同土地利用方式下[18]和不同农业种植模式下[19, 20]水土流失造成的面源污染上, 对库区特有的反复“淹水-落干”状态下, 消落带土壤磷释放过程与机制关注不够.且经过十多年的干湿交替后, 消落带土壤磷分布格局又产生了新的变化, 而消落带磷的释放特征仍不清楚, 对于未来三峡水库支流水污染控制构成新的挑战.
目前, 国际上学者大多选择磷素饱和度(degree of phosphorus sorption, DPS)作为土壤磷释放风险的指标.DPS是土壤中可提取态磷(soil text phosphorus, STP)占土壤磷最大吸附容量(phosphorus sorption capacity, PSC)的百分比[21, 22].STP根据提取方式的不同而呈现较大差异, 选择土壤中生物有效性较高的形态磷之和作为生物有效磷(bioavailable phosphorus, Bio-P)[23], 涵盖范围更全面, 在评价三峡消落带土壤磷释放风险中得到了较好运用[23].本文也将利用学者提出的DPS经验公式和阈值研究三峡库区消落带土壤磷流失现状和风险.
1 材料与方法 1.1 研究区概况和样品采集三峡库区重庆段消落带占库区消落带总面积的87.8%, 重庆段涪陵以下至云阳的库区腹心段区县消落带面积占全市消落带面积的84.3%[24].其中, 涪陵多为斜坡淹没形成的消落带, 忠县多为台地和阶地淹没后形成的消落带, 且为大暴雨集中中心.该地区为亚热带湿润季风气候, 年平均气温为18.5℃, 年平均降水量为1 140 mm, 其中约70%发生在雨季(5~9月).因此, 选择涪陵珍溪河(FLZX)、忠县黄金河(ZXHJ)和忠县汝溪河坪山(ZXPS)库湾作为研究地点(图 1), 代表三峡库区腹心库湾消落带.3个研究地点分别距离长江干流约0.7、1.5和3.0 km, 整体坡度分别为30°~60°左右.消落带150 m以下为沉积泥沙; 150~160 m优势植物为狗牙根和水蓼, 狗牙根占比约90%以上; 160~175 m优势植物为苍耳、鬼针草和蒿草, 植被盖度随高程增加逐渐提高.珍溪河和黄金河175 m以上土壤被开垦成农田, 种植豆类和玉米等农作物, 而坪山库湾多种植果树, 如柑橘等.
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图 1 三峡库区消落带采样样点 Fig. 1 Location of sampling sites in tributaries, Three Gorges Reservoir |
2019年6月18~19日, 待库区水位降至148 m左右进行采样.分别在各个研究点设置3条采样断面, 各断面之间距离约200 m左右.断面由低到高设置4个采样高程, 分别为150、160、170和180 m.选择175 m以上、未被人为活动干扰和未经历过干湿交替影响的区域采集180 m土壤样品, 作为下方消落带的对照土壤.根据均匀分布和典型代表原则, 在各个高程采集3~5处表层土壤样品(0~20 m), 将土壤样品装袋带回实验室.将同一断面、同一高程的土壤样品混合均匀, 挑出植物根系, 分出小部分冷藏保存, 剩余样品自然风干, 粉碎后过10目和100目筛, 室温保存.
1.2 指标测定土壤鲜样直接测定无机磷(IP)形态、碱性磷酸酶(alkaline phosphomonoesterase, ALP)和磷酸二酯酶(phosphodiesterase, PDE), 风干土测定粒径组成、pH、总磷(TP)、有机质(OM)和有机磷(OP)形态.吸管法测定粒径组成, 分为黏粒(<0.002 mm)、粉粒(0.002~0.05 mm)和砂粒(0.05~2 mm)[25].NaOH熔融法提取TP.pH计测定土壤pH(水土比, 2.5 ∶1).重铬酸钾-硫酸亚铁铵法测定OM.ALP和PDE活性采用对-硝基苯磷酸二钠和双(对-硝基苯基)磷酸酯比色法测定(以p-NP计)[26].
IP形态采用Chang等[27]和Buehler等[28]提出的改进后的无机磷分级方法, 1.0 mol ·L-1 NH4Cl(pH值为8.0)提取交换态磷(Ex-P); 0.5 mol ·L-1 NH4F(pH值为8.2)提取铝结合态磷(Al-P); 0.1 mol ·L-1 NaOH提取铁结合态磷(Fe-P); 0.3 mol ·L-1柠檬酸钠+连二亚硫酸钠混合溶液提取闭蓄态磷(Oc-P); 0.5 mol ·L-1 H2SO4提取钙结合态磷(Ca-P).
OP形态采用Ivanoff等[29]提出的有机磷分级方法, 0.5 mol ·L-1 NaHCO3(pH值为8.5)提取活性有机磷(NaHCO3-Po); 1 mol ·L-1 HCl提取酸结合态有机磷(HCl-Po); 0.5 mol ·L-1 NaOH提取富里酸结合态有机磷(Fulvic-Po)和胡敏酸结合态有机磷(Humic-Po), 分别为上清液和沉淀中的有机磷; 剩余样品灼烧后用1 mol ·L-1 H2SO4提取残余态有机磷(Residual-Po).
1.3 土壤生物有效磷、磷吸附指数和磷素饱和度根据无机磷和有机磷中各形态磷的活性大小, 以Ex-P、Al-P、Fe-P、NaHCO3-Po、HCl-Po和Fulvic-Po之和作为土壤Bio-P[30].
PSC包含土壤可吸附磷和已固存磷, 通常利用浸提液中铝和铁的含量代替PSC, 但这种方法多适用于酸性土壤.针对这一问题, 学者提出利用磷吸附指数(phosphorus sorption index, PSI)与特定系数的乘积代替PSC[31]. PSI是按照Bache等[32]建议的方法, 土壤样品(1 g风干土)用20 mL 0.01 mol ·L-1 CaCl2溶液(含75 mg ·L-1 H2PO4-P)平衡24 h, 并在(25±1)℃下振荡, 滤液测定残余磷含量.PSI计算公式如下:
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(1) |
式中, X为土壤吸附磷含量(mg ·kg-1), c为滤液残余磷浓度(mg ·L-1).
根据ω(Bio-P)和PSC计算土壤DPS(%), 公式如下:
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(2) |
数据经Excel 2016处理后, 采用One way-ANOVA方法对数据进行显著性分析, 用最小显著极差法(Duncan)确定差异显著性水平.用冗余分析(RDA)辨别土壤磷形态的分布转化特征, 以及与土壤理化性质之间的相关性.数据的统计分析用IBM SPSS 22和CANOCO 5.0, 使用Origin 9.0绘图.文中所示误差, 如无说明, 均为3个重复测定的标准差(n=3).
2 结果与分析 2.1 土壤理化性质各支流库湾土壤理化性质如表 1所示.土壤均以砂粒和黏粒为主, 质量分数均值达30%以上.除黄金河170 m高程土壤外, 其余支流土壤pH均为中性和弱碱性.支流消落带土壤OM含量随高程增加逐渐增大, 160 m高程以上土壤OM含量显著高于对照土壤(P < 0.05). 160 m高程土壤ALP和PDE活性均显著高于其余高程土壤(P < 0.05).
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表 1 三峡库区不同高程土壤理化性质1) Table 1 Physical and chemical properties of soils with altitude in the Three Gorges Reservoir |
2.2 磷赋存形态 2.2.1 总磷
消落带土壤ω(TP)为524.36~1 092.66 mg ·kg-1, 均值为771.80mg ·kg-1(图 2).各消落带土壤TP含量在高程间分布趋势不明确, 与对照土壤差异不一致.
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不同小写字母表示不同高程差异显著(P < 0.05) 图 2 三峡库区支流不同高程土壤总磷含量 Fig. 2 Contents of TP in soils with altitude in tributaries, Three Gorges Reservoir |
消落带土壤可提取ω(IP)为272.78~762.41mg ·kg-1, 均值为485.33mg ·kg-1(图 3).土壤IP形态以Ca-P为主, 其余依次为Oc-P、Fe-P、Al-P和Ex-P, 不同形态磷含量排序与已有研究的结果相似[33, 34].3个库湾消落带土壤整体Ex-P和Oc-P含量均显著高于对照土壤.Fe-P含量随高程下降而显著降低, Oc-P含量随高程降低表现出先减小后增大的趋势, Ex-P、Al-P和Ca-P含量无明确分布趋势(P < 0.05).
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(a)、(d)和(g)FLZX, (b)、(e)和(h)ZXHJ, (c)、(f)和(i)ZXPS; 小写字母为同一形态磷的不同高程比较, 不同小写字母表示不同高程差异显著(P < 0.05) 图 3 三峡库区支流不同高程土壤无机磷形态含量 Fig. 3 Contents of IP in soils with altitude in tributaries, Three Gorges Reservoir |
消落带土壤可提取ω(OP)为90.02~239.42 mg ·kg-1, 均值为166.30 mg ·kg-1(图 4).土壤OP以Residual-Po为主, 其余依次为Fulvic-Po、HCl-Po、Humic-Po和NaHCO3-Po, 与已有研究结果相似[35~37].消落带土壤NaHCO3-Po含量显著高于对照土壤(P < 0.05).在高程间, HCl-Po、Fulvic-Po和Residual-Po含量均随高程降低而显著降小, NaHCO3-Po和Humic-Po分布趋势不明确(P < 0.05).
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(a)、(d)和(g)FLZX, (b)、(e)和(h)ZXHJ, (c)、(f)和(i)ZXPS; 小写字母为同一形态磷的不同高程比较, 不同小写字母表示不同高程差异显著(P < 0.05) 图 4 三峡库区支流不同高程土壤有机磷形态含量 Fig. 4 Contents of OP in soils with altitude in tributaries, Three Gorges Reservoir |
支流库湾消落带土壤ω(Bio-P)为49.19~148.78mg ·kg-1, 占TP的质量分数为7.71% ~24.78%(表 2).Bio-P含量和质量分数均沿高程降低而显著下降, PSI与之类似(P < 0.05).消落带土壤DPS为5.85% ~22.00%, 分布趋势与Bio-P一致.除黄金河160 m高程以上土壤外, 其余消落带土壤DPS均显著低于对照土壤(P < 0.05).
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表 2 三峡库区支流不同高程土壤有效磷和磷素饱和度1) Table 2 Bioavailable phosphorus and degree of phosphorus saturation in soils with altitude in tributaries, Three Gorges Reservoir |
3 讨论 3.1 反复干湿交替对消落带土壤磷形态赋存的影响
IP形态中, Ex-P、Al-P和Fe-P均属于生物可利用无机磷[38, 39].多年干湿交替作用下, Fe-P在高程间形成逐级减少的格局, 与已有研究结果相似[33]. 150 m高程土壤淹水时间较长, 缺氧环境下还原作用加强, 使得铁氧化物被持续还原, 磷酸盐大量释放; 170 m高程土壤落干时间较长, 氢氧化铁氧化后吸附游离的磷酸盐重新保存下来[33, 40].Ex-P靠物理吸附附着于土壤微粒和有机质表面, 当环境水分变化时, 吸附的磷可直接脱落进入间隙水[41].Al-P活性较高, 铝氧化物形态受pH影响较大.
OP形态中, NaHCO3-Po、HCl-Po和Fulvic-Po属于生物可利用有机磷.NaHCO3-Po与Ex-P类似, 消落带土壤Ex-P和NaHCO3-Po均显著高于对照土壤(图 3), 这与前人研究的结果相反[41~44].在考虑活性磷流失的同时, 可能忽略了Fe-P转化和非活性有机磷活化等过程(图 5).HCl-Po和Fulvic-Po赋存格局与Fe-P类似, 在已有研究中也有相似的发现[45, 46].以上2种形态磷在有机磷中占大部分比例, 其含量变化与微生物和植物的生长死亡过程密切相关. 春夏出露期, 光照降雨集中, 有利于动植物生长和微生物繁殖, 增加了表层土壤有机磷的内源积累; 秋冬覆水时, 消落带土壤大部分微生物细胞因渗透压的突变, 导致细胞破裂, 溶解释放磷素, 有机磷含量降低[39].在此过程中, 消落带各高程土壤水分、雨热和营养物质差异较大, 优势植物分层显著, 动植物的生长死亡过程导致有机磷呈逐级递减的特征.
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红蓝线分别表示解释和响应变量, 下同 图 5 三峡库区支流消落带土壤磷形态与土壤有效磷和磷素饱和度冗余分析 Fig. 5 Redundancy analysis of soil phosphorus forms with Bio-P and DPS in WLFZ of tributaries, Three Gorges Reservoir |
因此, 干湿交替对消落带土壤生物可利用形态磷的影响机制包括:①土壤水分环境的变化直接影响活性磷的附着状态; ②土壤氧化还原条件和pH的变化使得铁铝氧化物与磷酸盐的结合方式发生转变, 磷酸盐被释放或重新结合; ③植物和微生物生长死亡过程使得土壤有机质迅速积累和消耗, 淹水-落干的时间差异导致有机磷梯级分布.
3.2 消落带土壤磷释放风险吴起鑫等[41]和徐德星等[47]对消落带形成初期土壤Bio-P质量分数的研究结果分别为25.18% ~65.38%和54%, 本研究中Bio-P质量分数均低于25%, 表明多年干湿交替使得消落带土壤Bio-P大量流失.在已有研究中, DPS≥25%可作为一个临界值, 高于该临界值时土壤具有较高的可解吸磷会随径流或壤中流释放[22].3个消落带土壤DPS均低于22%, 且在高程间逐级降低.目前, 当处于淹水状态且水流无较大波动时, 支流库湾消落带土壤磷素释放风险较低, 170 m高程土壤磷释放风险最高.结合三峡库区消落带坡耕地土壤磷流失过程的原位监测研究, 消落带土壤主要的磷释放途径可能集中在夏季时期降雨导致的水土流失, 即不可逆转的磷素迁移过程[48~50].
经历干湿交替时, 各形态磷结合方式的不同导致土-水界面磷酸盐释放过程差异较大[7].通过各形态磷与Bio-P和DPS的冗余分析可知, HCl-Po和Fulvic-Po与Bio-P以及Fe-P与DPS之间夹角较小且箭头长度较长, 存在显著的正相关关系(图 5).以上形态磷在磷释放过程中的贡献率可达98.6%, 是生物可利用磷的主要来源, 与含量大小有直接关系.三者与土壤理化性质的冗余分析显示, pH、OM和ALP的解释度可达68.5%(图 6).pH对Fe-P为负反馈作用, ALP和OM对HCl-Po和Fulvic-Po均为正反馈作用.有研究表明, 土壤中较高的OH-可以与磷酸盐阴离子争夺氧化物吸附点位, 导致与铁氧化物结合的磷酸根释放量增加[33].磷酸酶主要由植物和微生物分泌, 是土壤磷素循环和能量流动的重要参与者.高艺伦[51]对澎溪河消落带不同高程土壤磷形态和磷酸酶活性进行了研究, 发现整体上消落带土壤磷酸酶活性与各有机磷含量呈显著正相关.OM是有机磷的重要来源, 在土壤缺磷时可被磷酸酶活化, 形成新的有机磷参与土壤磷素循环[46].
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图 6 三峡库区消落带土壤高释放风险磷形态与土壤理化性质冗余分析 Fig. 6 Redundancy analysis of phosphorus forms of high release risk with soil physical and chemical properties in WLFZ of tributaries, Three Gorges Reservoir |
(1) 消落带土壤ω(TP)、ω(IP)和ω(OP)均值分别为771.80、485.33、166.30 mg ·kg-1.无机磷和有机磷不同形态磷含量排序分别为:Ca-P>Oc-P>Fe-P>Al-P>Ex-P和Residual-Po>Fulvic-Po>HCl-Po>Humic-Po>NaHCO3-Po, 均以非活性磷为主, 整体生物有效性较低.
(2) 消落带土壤Ex-P和NaHCO3-Po含量显著高于对照土壤, Fe-P、HCl-Po和Fulvic-Po含量随高程下降而显著降低.活性磷和中等活性磷在高程间的赋存格局与干湿交替下土壤环境的变化有关.
(3) 消落带土壤ω(Bio-P)为49.19~148.78 mg ·kg-1, 占TP的质量分数为7.71% ~24.78%, 远低于消落带形成初期研究结果.消落带土壤DPS为5.85% ~22.00%, 低于已有研究中根据土壤磷释放风险划定的最低阈值(25%).目前, 当处于淹水状态且水流无较大波动时, 消落带土壤磷释放风险较低.Fe-P、HCl-Po和Fulvic-Po在磷释放过程中贡献率最大, 土壤pH、OM和ALP活性的变化是导致磷释放的主要原因, 在后续库区支流水环境治理防护中以上形态磷需要重点关注.
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