干旱区研究 ›› 2023, Vol. 40 ›› Issue (6): 905-915.doi: 10.13866/j.azr.2023.06.06
张颂安1(),刘轩1,赵珮杉1,高广磊1,2,3(),张英1,3,丁国栋1,2,3,柳叶1,任悦1
收稿日期:
2022-09-21
修回日期:
2022-12-07
出版日期:
2023-06-15
发布日期:
2023-06-21
通讯作者:
高广磊. E-mail: 作者简介:
张颂安(1997-),女,硕士研究生,主要研究方向为荒漠化防治. E-mail: 基金资助:
ZHANG Songan1(),LIU Xuan1,ZHAO Peishan1,GAO Guanglei1,2,3(),ZHANG Ying1,3,DING Guodong1,2,3,LIU Ye1,REN Yue1
Received:
2022-09-21
Revised:
2022-12-07
Online:
2023-06-15
Published:
2023-06-21
摘要:
为揭示呼伦贝尔沙地樟子松人工林土壤细菌相互关系,以呼伦贝尔沙地不同林龄樟子松人工林(25 a、34 a和43 a)为研究对象,以沙质草地为对照,采用分子生态网络分析法对不同土层(0~10 cm和10~20 cm)土壤细菌群落进行比较分析。结果表明:(1) 从25 a到43 a,土壤细菌网络总边数增多,平均路径长度降低。土壤深度由0~10 cm到10~20 cm,人工林土壤细菌网络总边数减少,平均路径长度升高。与沙质草地相比,人工林土壤细菌网络总边数较少。(2) 25 a人工林关键菌种隶属于嗜酸菌目(Acidimicrobiales)、RB41和MB-A2-108,34 a人工林关键菌种隶属于Gaiellales,43 a人工林关键菌种隶属于Gaiellales、RB41、Subgroup_7、Subgroup_6、和DA101_soil_group,草地关键菌种隶属于匿杆菌门(Latescibacteria)。(3) 全氮、氨氮、微生物碳含量和脲酶酶活性对土壤细菌网络中具有高中介中心性的部分细菌有显著正相关影响(P<0.05);转化酶和过氧化氢酶活性、土壤含水量以及速效磷含量对土壤细菌网络中具有高中介中心性的部分细菌有显著负相关影响(P<0.05);土壤有机质对土壤细菌网络中具有高中介中心性的部分细菌既有显著正相关影响又有显著负相关影响(P<0.05)。樟子松人工林从25 a到43 a,土壤细菌网络愈加复杂和紧密,土壤深度由0~10 cm到10~20 cm,网络复杂性和紧密度降低;与草地相比,人工林土壤细菌网络复杂性较低。43 a人工林土壤细菌网络关键菌种类型数量最多。另外,土壤细菌网络受土壤有机质影响最大。研究结果有助于深入理解呼伦贝尔沙地樟子松人工林土壤细菌群落,并为呼伦贝尔沙地樟子松人工林的可持续经营提供科技支撑。
张颂安, 刘轩, 赵珮杉, 高广磊, 张英, 丁国栋, 柳叶, 任悦. 呼伦贝尔沙地樟子松人工林土壤细菌网络特征[J]. 干旱区研究, 2023, 40(6): 905-915.
ZHANG Songan, LIU Xuan, ZHAO Peishan, GAO Guanglei, ZHANG Ying, DING Guodong, LIU Ye, REN Yue. Soil bacterial networks in Pinus sylvestris var. mongolica plantations of the Hulunbuir Desert[J]. Arid Zone Research, 2023, 40(6): 905-915.
表3
呼伦贝尔沙地樟子松人工林土壤细菌网络拓扑特征"
拓扑特征 | HLP25A | HLP25B | HLP34A | HLP34B | HLP43A | HLP43B | HLGA | HLGB | |
---|---|---|---|---|---|---|---|---|---|
经验网络 | 节点 | 306 | 304 | 307 | 292 | 300 | 268 | 330 | 325 |
边 | 2395 | 2262 | 2483 | 2313 | 3072 | 2011 | 2689 | 2831 | |
平均连通度 | 15.65 | 14.88 | 16.18 | 15.84 | 20.48 | 15.01 | 16.30 | 17.42 | |
模块化 | 0.75 | 0.77 | 0.70 | 0.72 | 0.62 | 0.62 | 0.71 | 0.71 | |
平均路径长度 | 11.89 | 15.26 | 11.50 | 11.67 | 8.57 | 13.81 | 12.14 | 11.52 | |
平均聚类系数 | 0.75 | 0.74 | 0.75 | 0.75 | 0.76 | 0.74 | 0.74 | 0.75 | |
正相关/% | 54.53 | 51.50 | 52.56 | 49.72 | 52.96 | 50.22 | 48.83 | 53.27 | |
负相关/% | 45.47 | 48.50 | 47.44 | 50.28 | 47.04 | 49.78 | 51.17 | 46.73 | |
随机网络 | 模块化 | 0.21 | 0.21 | 0.20 | 0.20 | 0.18 | 0.21 | 0.21 | 0.20 |
平均路径长度 | 2.37 | 2.41 | 2.35 | 2.34 | 2.16 | 2.35 | 2.37 | 2.32 | |
平均聚类系数 | 0.05 | 0.05 | 0.06 | 0.05 | 0.07 | 0.05 | 0.05 | 0.05 |
表4
呼伦贝尔沙地樟子松人工林土壤细菌网络连接节点"
关键菌种 | OTU | 门 | 纲 | 目 | 科 | 属 |
---|---|---|---|---|---|---|
HLP25A | OTU144 | Actinobacteria | Acidimicrobiia | Acidimicrobiales | - | - |
HLP25B | OTU182 | Acidobacteria | Blastocatellia | Blastocatellales | Blastocatellaceae_Subgroup_4 | RB41 |
OTU291 | Actinobacteria | MB-A2-108 | - | - | - | |
HLP34A | OTU149 | Actinobacteria | Thermoleophilia | Gaiellales | - | - |
HLP34B | - | - | - | - | - | - |
HLP43A | OTU66 | Acidobacteria | Blastocatellia | Blastocatellales | Blastocatellaceae_Subgroup_4 | RB41 |
OTU677 | Acidobacteria | Holophagae | Subgroup_7 | - | - | |
OTU319 | Acidobacteria | Subgroup_6 | - | - | - | |
OTU556 | Verrucomicrobia | Spartobacteria | Chthoniobacterales | DA101_soil_group | - | |
HLP43B | OTU152 | Acidobacteria | Subgroup_6 | - | - | - |
OTU3844 | Acidobacteria | Thermoleophilia | Gaiellales | - | - | |
HLGA | - | - | - | - | - | - |
HLGB | OTU718 | Latescibacteria | - | - | - | - |
表5
呼伦贝尔沙地樟子松人工林土壤理化性质与酶活性"
土壤因子 | HLP25A | HLP25B | HLP34A | HLP34B | HLP43A | HLP43B | HLGA | HLGB |
---|---|---|---|---|---|---|---|---|
土壤含水量SWC/% | 10.44±3.66a | 5.77±1.39A | 9.00±1.27a | 6.66±0.78A | 6.88±0.47b | 5.81±2.08A | 10.18±0.89a | 7.69±1.35A |
全氮TN/(g·kg-1) | 0.82±0.01b | 0.56±0.01C | 0.77±0.01c | 0.63±0.00A | 0.51±0.03d | 0.49±0.01D | 0.93±0.02a | 0.59±0.01B |
土壤有机质SOM /(g·kg-1) | 2.31±0.06a | 1.90±0.05A | 2.11±0.05b | 1.82±0.02AB | 1.71±0.12c | 1.32±0.06C | 2.01±0.08b | 1.74±0.06B |
氨氮AN/(mg·kg-1) | 45.37±3.08ab | 84.73±1.59A | 43.30±2.19b | 44.57±2.99B | 50.06±3.36a | 30.63±5.17C | 49.82±3.67a | 44.12±0.57B |
速效磷AP/(g·kg-1) | 3.87±0.31a | 3.35±0.51A | 6.11±1.44a | 4.93±0.30A | 5.40±1.96a | 5.07±0.84A | 4.13±0.65a | 3.28±1.86A |
过氧化氢酶CA/(U·g-1) | 938.76±31.28b | 545.09±528.63AB | 132.00±38.11c | 172.64±7.02B | 997.95±4.60a | 921.19±29.80A | 992.65±22.58a | 884.29±25.03A |
转化酶IA/(U·g-1) | 70.92±6.00c | 41.24±2.36B | 69.63±1.11c | 41.64±7.94B | 97.93±3.00a | 48.94±6.24B | 81.17±4.79b | 74.61±8.92A |
脲酶SU/(U·g-1) | 635.42±35.36a | 213.98±68.25A | 396.04±43.47c | 251.52±20.26A | 511.12±26.12b | 223.20±162.05A | 155.32±28.05d | 258.03±26.61A |
微生物碳MC /(mg·kg-1) | 21.58±12.89c | 18.52±14.02B | 73.09±1.78a | 44.89±2.15A | 14.32±1.74c | 11.60±3.30B | 59.32±4.63b | 51.75±1.16A |
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