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  • CN 62-1070/P
  • ISSN 1000-694X
  • Bimonthly 1981
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Community dynamics of ground arachnid arthropods in a gravel gobi desert of the middle of the Hexi Corridor, China

  • Jiliang Liu ,
  • Wenzhi Zhao ,
  • Fengrui Li ,
  • Yibin Ba
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  • 1.Linze Inland River Basin Research Station,Northwest Institute of Eco-Environment and Resources,Chinese Academy of Sciences,Lanzhou 730000,China
    2.University of Chinese Academy of Sciences,Beijing 100049,China
    3.Museum of Hebei University,Baoding 071002,Hebei,China

Received date: 2020-06-24

  Revised date: 2021-02-04

  Online published: 2021-05-26

Abstract

Gobi was a key desert type, and it accounts for 50% of the total area of the Hexi Corridor. Arachnid arthropods are mainly predatory arthropods, and they play an important role in the food webs of the gobi desert ecosystem. In this paper, we select a typical gravel gobi desert in the middle of the Hexi Corridor as a long-term observation site for arachnid arthropods. Ground arachnid arthropods was collected using pitfall trap from January to December in 2018 and 2019, and microclimate variable was also monitoring. Based on the above research, we found that Arachnida community is composed of 4 orders, 12 families and 22 species, and Gnaphosidae, Philodromidae, Theridiidae, Thomisidae, Sclerosomatidae, and Karschiidaeare dominant arachnid arthropods, and Steatoda albomaculataXysticus spp., Philodromus spp., Gnaphosa spp., Mesobuthus martensiiMitopus morio, and Karschia sp. are dominant species. The pattern of monthly activity density and species richness was consistent from 2018 to 2019. The activity density of ground arachnid arthropods were peaked in April of 2018, and this pattern was found in June of 2019. Gnaphosidae, Karschiidae, Philodromidae, Sclerosomatidae, Thomisidae, and Theridiidae were dominant families, the activity of Thomisidae, Sclerosomatidae, and Karschiidae in 2019 was higher than that in 2018, and an opposite trend in Gnaphosidae, Philodromidae, and Theridiidae. Monthly activity density of arachnid arthropods showed significant monthly and annual variation. The active period of Philodromidae was in the spring, the activity density of philodromid spiders was peaked in March of 2018 and 2019. The active period of Thomisidae and Sclerosomatidae was in the autumn, the activity density of thomisid spiders was peaked in August of 2018 and 2019, and the activity density of Sclerosomatidae was peaked in October and August of 2018 and 2019. The activity density of Gnaphosidae, Karschiidae, and Theridiidae was peaked in April of 2018, and these patterns were found in June or September of 2019. The activity density and group richness of arachnid arthropods were significant quadratic correlations with monthly average temperature, and no significant correlations with monthly precipitation. In addition, we also found that the activity density of Buthidae was significant positive correlations with monthly average temperature and precipitation, the activity density of Thomisidae was significant positive correlations with monthly precipitation, the activity density of Lycosidae and Gnaphosidae was significant positive correlations with monthly average temperature. In short, temperature and precipitation changes are important influence factors for day, month, season and year activity rhythm in ground arachnid arthropods, which regulate the community dynamic of arachnid arthropods in the gravel gobi desert.

Cite this article

Jiliang Liu , Wenzhi Zhao , Fengrui Li , Yibin Ba . Community dynamics of ground arachnid arthropods in a gravel gobi desert of the middle of the Hexi Corridor, China[J]. Journal of Desert Research, 2021 , 41(3) : 155 -164 . DOI: 10.7522/j.issn.1000-694X.2021.00013

References

1 冯益明,吴波,周娜,等.基于遥感影像识别的戈壁分类体系研究[J].中国沙漠,2013,33(3):635-641.
2 冯益明,吴波,姚爱冬,等.戈壁分类体系与编目研究[J].地理学报,2014,69(3):391-398.
3 申元村,王秀红,程维明,等.中国戈壁综合自然区划研究[J].地理科学进展,2016,35(1):57-66.
4 于琳倩,李景文,李俊清,等.中国沙漠、戈壁自然资源分类体系及其组成特点[J].内蒙古农业大学学报(自然科学版),2014,35(1):59-66.
5 Whitford W G.The importance of the biodiversity of soil biota in arid ecosystems[J].Biodiversity and Conservation,1996,5:185-195.
6 Polis G A,Yamashita T.The ecology and importance of predaceous arthropods in desert communities[M]//Polis G A.The Ecology of Desert Communities.Tuscon,USA:The University of Arizona Press,1991:180-222.
7 刘继亮,李锋瑞,刘七军,等.黑河中游干旱荒漠地面节肢动物群落季节变异规律[J].草业学报,2010,19(5):161-169.
8 Song D X,Zhu M S,Chen J.The Spiders of China[M].Shijiazhuang:Hebei Science and Technology Publishing House,1999.
9 胡金林.青藏高原蜘蛛[M].郑州:河南科学技术出版社,2001.
10 张志升,王露雨.中国蜘蛛生态大图鉴[M].重庆:重庆大学出版社,2017.
11 Richman D B,Brantley S.Spiders of the Chihuahuan Desert of Southern New Mexico and Western Texas[J].The Southwestern Naturalist,2011,56:44-53.
12 刘继亮,李锋瑞,牛瑞雪,等.黑河中游不同土地利用方式地面节肢动物对土壤盐渍化的响应[J].土壤学报,2011,48(6):1242-1252.
13 蒯国锋,刘新民.沙坡头地区人工植被条件下土壤蜘蛛群落特征的研究[J].内蒙古师范大学学报(自然科学汉文版),2004,33(3):304-307.
14 Griffin R E.Species richness and biogeography of non-acarine arachnids in Namibia[J].Biodiversity & Conservation,1998,7:467-481.
15 Shi C M,Liang H B,Altanchimeg D,et al.Climatic niche defines geographical distribution of Mesobuthus eupeusmongolicus (Scorpions:Buthidae) in gobi desert[J].Zoological Systematics,2015,40(3):339-348.
16 刘刚,马祁,姚举,等.棉田与相邻荒漠过渡带蜘蛛群落结构及动态分析[J].新疆农业科学,2007(3):298-302.
17 Pluess T,Opatovsky I,Gavish-Regev E,et al.Non-crop habitats in the landscape enhance spider diversity in wheat fields of a desert agroecosystem[J].Agriculture Ecosystems & Environment,2010,137:68-74.
18 Cloudsley-Thompson J L.Desert adaptation in spiders[J].Journal of Arid Environments,1983,6:307-317.
19 Cloudsley-Thompson J L.Ecophysiology of desert Arachnida[J].Bollettino dell’Accademia Gioenia di Scienze Naturali,1993,26(345):53-63.
20 Langlands P R,Brennan K E C,Pearson D J.Spiders,spinifex,rainfall and fire:Long-term changes in an arid spider assemblage[J].Journal of Arid Environments,2006,67:36-59.
21 Li F,Zhao W Z,Liu H.The response of aboveground net primary productivity of desert vegetation to rainfall pulse in the temperate desert region of northwest China[J].PLoS One,2013,8:e73003.
22 Taucare-?ios A,Veloso C,Canals M,et al.Daily thermal preference variation of the sand recluse spider Sicarius thomisoides (Araneae:Sicariidae)[J].Journal of Thermal Biology,2019,87:102465.
23 MacKay W P,Grimsley C,Cokendolpher J C.Seasonal changes in a population of desert harvestmen,Trachyrhinus Marmoratus (Arachnida:Opiliones),from Western Texas[J].Psyche,99:207-213.
24 Liu J L,Li F R,Liu L L,et al.Responses of different Collembola and mite taxa to experimental rain pulses in an arid ecosystem[J].Catena,2017,155:53-61.
25 Kwok A B C,Wardle G M,Greenville A C,et al.Long-term patterns of invertebrate abundance and relationships to environmental factors in arid Australia[J].Austral Ecology,2016,41:480-491.
26 Lensing J R,Todd S,Wise D H.Theimpactofalteredprecipitationonspatialstrati?cation and activity-densities of springtails (Collembola) and spiders (Araneae)[J].Ecology Entomology,2005,30:194-200.
27 Cloudsley-Thompson J L.Adaptations of arthropoda to arid environments[J].Annual Review of Entomology,1975,20(1):261-283.
28 Webber M M,Bryson Jr R W.Geographic variation in the thermal biology of a widespread Sonoran Desert arachnid,Centruroides sculpturatus (Arachnida:Scorpiones)[J].Journal of Arid Environments,2015,121:40-42.
29 Lubin Y D,Henschel J R.Foraging at the thermal limit:burrowing spiders (Seothyra,Eresidae) in the Namib Desert dunes[J].Oecologia,1990,84(4):461-467.
30 Polis G A,Myers C,Quinlan M.Burrowing biology and spatial distribution of desert scorpions[J].Journal of Arid Environments,1986,10(2):137-146.
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