Articles | Volume 7, issue 2
https://doi.org/10.5194/soil-7-611-2021
© Author(s) 2021. This work is distributed under
the Creative Commons Attribution 4.0 License.
the Creative Commons Attribution 4.0 License.
https://doi.org/10.5194/soil-7-611-2021
© Author(s) 2021. This work is distributed under
the Creative Commons Attribution 4.0 License.
the Creative Commons Attribution 4.0 License.
The role of ecosystem engineers in shaping the diversity and function of arid soil bacterial communities
Zuckerberg Institute for Water Research, Blaustein Institutes for
Desert Research, Ben-Gurion University of the Negev, Midreshet Ben-Gurion,
Israel
Arielle M. Farrell
Mitrani Department of Desert Ecology, Swiss Institute for Dryland Environmental and Energy Research, Blaustein Institutes for Desert Research,
Ben-Gurion University of the Negev, Midreshet Ben-Gurion, Israel
Adam Št'ovíček
Department of Microbiology, Nutrition and Dietetics, Czech University
of Life Sciences Prague, Kamycka 129, Prague 6, 16500, Czech Republic
Lusine Ghazaryan
Zuckerberg Institute for Water Research, Blaustein Institutes for
Desert Research, Ben-Gurion University of the Negev, Midreshet Ben-Gurion,
Israel
Itamar Giladi
Mitrani Department of Desert Ecology, Swiss Institute for Dryland Environmental and Energy Research, Blaustein Institutes for Desert Research,
Ben-Gurion University of the Negev, Midreshet Ben-Gurion, Israel
Osnat Gillor
CORRESPONDING AUTHOR
Zuckerberg Institute for Water Research, Blaustein Institutes for
Desert Research, Ben-Gurion University of the Negev, Midreshet Ben-Gurion,
Israel
Related authors
Capucine Baubin, Noya Ran, Hagar Siebner, and Osnat Gillor
SOIL Discuss., https://doi.org/10.5194/soil-2021-88, https://doi.org/10.5194/soil-2021-88, 2021
Revised manuscript not accepted
Short summary
Short summary
In this manuscript, we describe changes in desert biocrust bacterial community during drought, rainfall, and dehydration in the Negev Desert. We followed the active bacterial community composition and their potential activity and showed that rainfall changes the bacterial community, triggers photosynthesis in soil phototrophs, and induces the production of extracellular polymeric substances that retain water during dehydration allowing bacterial cells to persist during the dehydration stage.
Talia Gabay, Eva Petrova, Osnat Gillor, Yaron Ziv, and Roey Angel
SOIL, 9, 231–242, https://doi.org/10.5194/soil-9-231-2023, https://doi.org/10.5194/soil-9-231-2023, 2023
Short summary
Short summary
This paper evaluates bacterial growth in biocrusts after a large-scale mining disturbance in a hyperarid desert, using a stable isotope probing assay.
We discovered that biocrust bacteria from both natural and post-mining plots resumed photosynthetic activity but did not grow following hydration. Our paper provides insights into the effects of a large-scale disturbance (mining) on biocrusts and their response to hydration, with implications for biocrust restoration practices in Zin mines.
Capucine Baubin, Noya Ran, Hagar Siebner, and Osnat Gillor
SOIL Discuss., https://doi.org/10.5194/soil-2021-88, https://doi.org/10.5194/soil-2021-88, 2021
Revised manuscript not accepted
Short summary
Short summary
In this manuscript, we describe changes in desert biocrust bacterial community during drought, rainfall, and dehydration in the Negev Desert. We followed the active bacterial community composition and their potential activity and showed that rainfall changes the bacterial community, triggers photosynthesis in soil phototrophs, and induces the production of extracellular polymeric substances that retain water during dehydration allowing bacterial cells to persist during the dehydration stage.
Nimrod Wieler, Tali Erickson Gini, Osnat Gillor, and Roey Angel
Biogeosciences, 18, 3331–3342, https://doi.org/10.5194/bg-18-3331-2021, https://doi.org/10.5194/bg-18-3331-2021, 2021
Short summary
Short summary
Biological rock crusts (BRCs) are common microbial-based assemblages covering rocks in drylands. BRCs play a crucial role in arid environments because of the limited activity of plants and soil. Nevertheless, BRC development rates have never been dated. Here we integrated archaeological, microbiological and geological methods to provide a first estimation of the growth rate of BRCs under natural conditions. This can serve as an affordable dating tool in archaeological sites in arid regions.
Nimrod Wieler, Hanan Ginat, Osnat Gillor, and Roey Angel
Biogeosciences, 16, 1133–1145, https://doi.org/10.5194/bg-16-1133-2019, https://doi.org/10.5194/bg-16-1133-2019, 2019
Short summary
Short summary
In stony deserts, when rocks are exposed to atmospheric conditions, they undergo weathering. The cavernous (honeycomb) weathering pattern is one of the most common, but it is still unclear exactly how it is formed. We show that microorganisms, which differ from the surrounding soil and dust, form biological crusts on exposed rock surfaces. These microbes secrete polymeric substances that mitigate weathering by reducing evaporation rates and, consequently, salt transport rates through the rock.
Related subject area
Soils and natural ecosystems
Mineral dust and pedogenesis in the alpine critical zone
Advancing studies on global biocrusts distribution
The soil knowledge library (KLIB) – a structured literature database on soil process research
Masked diversity and contrasting soil processes in tropical seagrass meadows: the control of environmental settings
Biocrust-linked changes in soil aggregate stability along a climatic gradient in the Chilean Coastal Range
Content of soil organic carbon and labile fractions depend on local combinations of mineral-phase characteristics
Effects of environmental factors and soil properties on soil organic carbon stock in a natural dry tropical area of Cameroon
SoilGrids 2.0: producing soil information for the globe with quantified spatial uncertainty
Disaggregating a regional-extent digital soil map using Bayesian area-to-point regression kriging for farm-scale soil carbon assessment
Opportunities and limitations related to the application of plant-derived lipid molecular proxies in soil science
Spatial variability in soil organic carbon in a tropical montane landscape: associations between soil organic carbon and land use, soil properties, vegetation, and topography vary across plot to landscape scales
A probabilistic approach to quantifying soil physical properties via time-integrated energy and mass input
Arctic soil development on a series of marine terraces on central Spitsbergen, Svalbard: a combined geochronology, fieldwork and modelling approach
Local versus field scale soil heterogeneity characterization – a challenge for representative sampling in pollution studies
Analysis and definition of potential new areas for viticulture in the Azores (Portugal)
The interdisciplinary nature of SOIL
Jeffrey S. Munroe, Abigail A. Santis, Elsa J. Soderstrom, Michael J. Tappa, and Ann M. Bauer
SOIL, 10, 167–187, https://doi.org/10.5194/soil-10-167-2024, https://doi.org/10.5194/soil-10-167-2024, 2024
Short summary
Short summary
This study investigated how the deposition of mineral dust delivered by the wind influences soil development in mountain environments. At six mountain locations in the southwestern United States, modern dust was collected along with samples of soil and local bedrock. Analysis indicates that at all sites the properties of dust and soil are very similar and are very different from underlying rock. This result indicates that soils are predominantly composed of dust delivered by the wind over time.
Siqing Wang, Li Ma, Liping Yang, Yali Ma, Yafeng Zhang, Changming Zhao, and Ning Chen
EGUsphere, https://doi.org/10.5194/egusphere-2023-2131, https://doi.org/10.5194/egusphere-2023-2131, 2023
Short summary
Short summary
Biological soil crusts (cover a substantial proportion of dryland ecosystem and play crucial roles in ecological processes. Consequently, studying the spatial distribution of biocrusts holds great significance. This study aimed to stimulate global-scale investigations of biocrusts distribution by introducing three major approaches. Then, we summarized present understandings of biocrusts distribution. Finally, we proposed several potential research topics.
Hans-Jörg Vogel, Bibiana Betancur-Corredor, Leonard Franke, Sara König, Birgit Lang, Maik Lucas, Eva Rabot, Bastian Stößel, Ulrich Weller, Martin Wiesmeier, and Ute Wollschläger
SOIL, 9, 533–543, https://doi.org/10.5194/soil-9-533-2023, https://doi.org/10.5194/soil-9-533-2023, 2023
Short summary
Short summary
Our paper presents a new web-based software tool to support soil process research. It is designed to categorize publications in this field according to site and soil characteristics, as well as experimental conditions, which is of critical importance for the interpretation of the research results. The software tool is provided open access for the soil science community such that anyone can contribute to improve the contents of the literature data base.
Gabriel Nuto Nóbrega, Xosé L. Otero, Danilo Jefferson Romero, Hermano Melo Queiroz, Daniel Gorman, Margareth da Silva Copertino, Marisa de Cássia Piccolo, and Tiago Osório Ferreira
SOIL, 9, 189–208, https://doi.org/10.5194/soil-9-189-2023, https://doi.org/10.5194/soil-9-189-2023, 2023
Short summary
Short summary
The present study addresses the soil information gap in tropical seagrass meadows. The different geological and bioclimatic settings caused a relevant soil diversity. Contrasting geochemical conditions promote different intensities of soil processes. Seagrass soils from the northeastern semiarid coast are marked by a more intense sulfidization. Understanding soil processes may help in the sustainable management of seagrasses.
Nicolás Riveras-Muñoz, Steffen Seitz, Kristina Witzgall, Victoria Rodríguez, Peter Kühn, Carsten W. Mueller, Rómulo Oses, Oscar Seguel, Dirk Wagner, and Thomas Scholten
SOIL, 8, 717–731, https://doi.org/10.5194/soil-8-717-2022, https://doi.org/10.5194/soil-8-717-2022, 2022
Short summary
Short summary
Biological soil crusts (biocrusts) stabilize the soil surface mainly in arid regions but are also present in Mediterranean and humid climates. We studied this stabilizing effect through wet and dry sieving along a large climatic gradient in Chile and found that the stabilization of soil aggregates persists in all climates, but their role is masked and reserved for a limited number of size fractions under humid conditions by higher vegetation and organic matter contents in the topsoil.
Malte Ortner, Michael Seidel, Sebastian Semella, Thomas Udelhoven, Michael Vohland, and Sören Thiele-Bruhn
SOIL, 8, 113–131, https://doi.org/10.5194/soil-8-113-2022, https://doi.org/10.5194/soil-8-113-2022, 2022
Short summary
Short summary
Soil organic carbon (SOC) and its labile fractions are influenced by soil use and mineral properties. These parameters interact with each other and affect SOC differently depending on local conditions. To investigate the latter, the dependence of SOC content on parameters that vary on a local scale depending on parent material, soil texture, and land use as well as parameter combinations was statistically assessed. Relevance and superiority of local models compared to total models were shown.
Désiré Tsozué, Nérine Mabelle Moudjie Noubissie, Estelle Lionelle Tamto Mamdem, Simon Djakba Basga, and Dieudonne Lucien Bitom Oyono
SOIL, 7, 677–691, https://doi.org/10.5194/soil-7-677-2021, https://doi.org/10.5194/soil-7-677-2021, 2021
Short summary
Short summary
Studies on soil organic carbon stock (SOCS) in the Sudano-Sahelian part of Cameroon are very rare. Organic C storage decreases with increasing latitude and more than 60 % of the SOCS is stored below the first 25 cm depth. In addition, a good correlation is noted between precipitation which decreases with increasing latitude and the total SOCS, indicating the importance of climate in the distribution of the total SOCS in the study area, which directly influence the productivity of the vegetation.
Laura Poggio, Luis M. de Sousa, Niels H. Batjes, Gerard B. M. Heuvelink, Bas Kempen, Eloi Ribeiro, and David Rossiter
SOIL, 7, 217–240, https://doi.org/10.5194/soil-7-217-2021, https://doi.org/10.5194/soil-7-217-2021, 2021
Short summary
Short summary
This paper focuses on the production of global maps of soil properties with quantified spatial uncertainty, as implemented in the SoilGrids version 2.0 product using DSM practices and adapting them for global digital soil mapping with legacy data. The quantitative evaluation showed metrics in line with previous studies. The qualitative evaluation showed that coarse-scale patterns are well reproduced. The spatial uncertainty at global scale highlighted the need for more soil observations.
Sanjeewani Nimalka Somarathna Pallegedara Dewage, Budiman Minasny, and Brendan Malone
SOIL, 6, 359–369, https://doi.org/10.5194/soil-6-359-2020, https://doi.org/10.5194/soil-6-359-2020, 2020
Short summary
Short summary
Most soil management activities are implemented at farm scale, yet digital soil maps are commonly available at regional/national scales. This study proposes Bayesian area-to-point kriging to downscale regional-/national-scale soil property maps to farm scale. A regional soil carbon map with a resolution of 100 m (block support) was disaggregated to 10 m (point support) information for a farm in northern NSW, Australia. Results are presented with the uncertainty of the downscaling process.
Boris Jansen and Guido L. B. Wiesenberg
SOIL, 3, 211–234, https://doi.org/10.5194/soil-3-211-2017, https://doi.org/10.5194/soil-3-211-2017, 2017
Short summary
Short summary
The application of lipids in soils as molecular proxies, also often referred to as biomarkers, has dramatically increased in the last decades. Applications range from inferring changes in past vegetation composition to unraveling the turnover of soil organic matter. However, the application of soil lipids as molecular proxies comes with several constraining factors. Here we provide a critical review of the current state of knowledge on the applicability of molecular proxies in soil science.
Marleen de Blécourt, Marife D. Corre, Ekananda Paudel, Rhett D. Harrison, Rainer Brumme, and Edzo Veldkamp
SOIL, 3, 123–137, https://doi.org/10.5194/soil-3-123-2017, https://doi.org/10.5194/soil-3-123-2017, 2017
Short summary
Short summary
We examined the spatial variability in SOC in a 10 000 ha landscape in SW China. The spatial variability in SOC was largest at the plot scale (1 ha) and the associations between SOC and land use, soil properties, vegetation, and topographical attributes varied across plot to landscape scales. Our results show that sampling designs must consider the controlling factors at the scale of interest in order to elucidate their effects on SOC against the variability within and between plots.
Christopher Shepard, Marcel G. Schaap, Jon D. Pelletier, and Craig Rasmussen
SOIL, 3, 67–82, https://doi.org/10.5194/soil-3-67-2017, https://doi.org/10.5194/soil-3-67-2017, 2017
Short summary
Short summary
Here we demonstrate the use of a probabilistic approach for quantifying soil physical properties and variability using time and environmental input. We applied this approach to a synthesis of soil chronosequences, i.e., soils that change with time. The model effectively predicted clay content across the soil chronosequences and for soils in complex terrain using soil depth as a proxy for hill slope. This model represents the first attempt to model soils from a probabilistic viewpoint.
W. Marijn van der Meij, Arnaud J. A. M. Temme, Christian M. F. J. J. de Kleijn, Tony Reimann, Gerard B. M. Heuvelink, Zbigniew Zwoliński, Grzegorz Rachlewicz, Krzysztof Rymer, and Michael Sommer
SOIL, 2, 221–240, https://doi.org/10.5194/soil-2-221-2016, https://doi.org/10.5194/soil-2-221-2016, 2016
Short summary
Short summary
This study combined fieldwork, geochronology and modelling to get a better understanding of Arctic soil development on a landscape scale. Main processes are aeolian deposition, physical and chemical weathering and silt translocation. Discrepancies between model results and field observations showed that soil and landscape development is not as straightforward as we hypothesized. Interactions between landscape processes and soil processes have resulted in a complex soil pattern in the landscape.
Z. Kardanpour, O. S. Jacobsen, and K. H. Esbensen
SOIL, 1, 695–705, https://doi.org/10.5194/soil-1-695-2015, https://doi.org/10.5194/soil-1-695-2015, 2015
J. Madruga, E. B. Azevedo, J. F. Sampaio, F. Fernandes, F. Reis, and J. Pinheiro
SOIL, 1, 515–526, https://doi.org/10.5194/soil-1-515-2015, https://doi.org/10.5194/soil-1-515-2015, 2015
Short summary
Short summary
Vineyards in the Azores have been traditionally settled on lava field terroirs whose workability and trafficability limitations make them presently unsustainable.
A landscape zoning approach based on a GIS analysis, incorporating factors of climate and topography combined with the soil mapping units suitable for viticulture was developed in order to define the most representative land units, providing an overall perspective of the potential for expansion of viticulture in the Azores.
E. C. Brevik, A. Cerdà, J. Mataix-Solera, L. Pereg, J. N. Quinton, J. Six, and K. Van Oost
SOIL, 1, 117–129, https://doi.org/10.5194/soil-1-117-2015, https://doi.org/10.5194/soil-1-117-2015, 2015
Short summary
Short summary
This paper provides a brief accounting of some of the many ways that the study of soils can be interdisciplinary, therefore giving examples of the types of papers we hope to see submitted to SOIL.
Cited articles
Alba-Lynn, C. and Detling, J. K.: Interactive disturbance effects of two disparate ecosystem engineers in North American shortgrass steppe, Oecologia, 157, 269–278, https://doi.org/10.1007/s00442-008-1068-0, 2008.
Angel, R.: Total Nucleic Acid Extraction from Soil, https://doi.org/10.1038/protex.2012.046, 2012.
Angel, R., Soares, M. I. M., Ungar, E. D., and Gillor, O.: Biogeography of soil archaea and bacteria along a steep precipitation gradient, ISME J., 4, 553–563, https://doi.org/10.1038/ismej.2009.136, 2010.
Bachar, A., Soares, M. I. M., and Gillor, O.: The effect of resource islands on abundance and diversity of bacteria in arid soils, Microb. Ecol., 63, 694–700, https://doi.org/10.1007/s00248-011-9957-x, 2012.
Baubin, C.: Soil metagenome Raw sequence reads, NCBI [data set], available at: https://www.ncbi.nlm.nih.gov/bioproject/?term=PRJNA484096,
last access: 30 September 2018.
Baubin, C., Farrell, A. M., Št'ovíček, A., Ghazaryan, L., Giladi, I., and Gillor, O.: Seasonal and spatial variability in total and active bacterial communities from desert soil, Pedobiologia, 74, 7–14, https://doi.org/10.1016/j.pedobi.2019.02.001, 2019.
Bay, S., Ferrari, B., and Greening, C.: Life without water: How do bacteria generate biomass in desert ecosystems?, Microbiology Australia, 39, 28–32, https://doi.org/10.1071/MA18008, 2018.
Ben-David, E. A., Zaady, E., Sher, Y., and Nejidat, A.: Assessment of the spatial distribution of soil microbial communities in patchy arid and semi-arid landscapes of the Negev Desert using combined PLFA and DGGE analyses, FEMS Microbiol. Ecol., 76, 492–503, https://doi.org/10.1111/j.1574-6941.2011.01075.x, 2011.
Berg, N. and Steinberger, Y.: Role of perennial plants in determining the activity of the microbial community in the Negev Desert ecosystem, Soil Biol. Biochem., 40, 2686–2695, https://doi.org/10.1016/j.soilbio.2008.07.019, 2008.
Borisov, V. B., Forte, E., Davletshin, A., Mastronicola, D., Sarti, P., and Giuffrè, A.: Cytochrome bd oxidase from Escherichia coli displays high catalase activity: An additional defense against oxidative stress, FEBS Lett., 587, 2214–2218, https://doi.org/10.1016/j.febslet.2013.05.047, 2013.
Bull, A. T.: Actinobacteria of the Extremobiosphere, in: Extremophiles Handbook, edited by: Horikoshi, K., Springer Japan, Tokyo, 1203–1240, 2011.
Callahan, B. J., McMurdie, P. J., Rosen, M. J., Han, A. W., Johnson, A. J. A., and Holmes, S. P.: DADA2: High-resolution sample inference from Illumina amplicon data, Nat. Methods, 13, 581–583, https://doi.org/10.1038/nmeth.3869, 2016.
Callaway, R. M.: Positive interactions among plants, Bot. Rev., 61, 306–349, 1995.
Chanal, A., Chapon, V., Benzerara, K., Barakat, M., Christen, R., Achouak, W., Barras, F., and Heulin, T.: The desert of Tataouine: an extreme environment that hosts a wide diversity of microorganisms and radiotolerant bacteria, Environ. Microbiol., 8, 514–525, https://doi.org/10.1111/j.1462-2920.2005.00921.x, 2006.
Cordero, P. R. F., Bayly, K., Man Leung, P., Huang, C., Islam, Z. F., Schittenhelm, R. B., King, G. M., and Greening, C.: Atmospheric carbon monoxide oxidation is a widespread mechanism supporting microbial survival, ISME J., 13, 2868–2881, https://doi.org/10.1038/s41396-019-0479-8, 2019.
de Graaff, M.-A., Adkins, J., Kardol, P., and Throop, H. L.: A meta-analysis of soil biodiversity impacts on the carbon cycle, SOIL, 1, 257–271, https://doi.org/10.5194/soil-1-257-2015, 2015.
Dinno, A.: Package “dunn.test,” CRAN Repos., 1–7, available at: https://cran.r-project.org/web/packages/dunn.test/dunn.test.pdf (last access: 5 March 2021), 2017.
Dunn, O. J.: Multiple Comparisons Using Rank Sums, Technometrics, 6, 241–252, 1964.
Facelli, J. M. and Temby, A. M.: Multiple effects of shrubs on annual plant communities in arid lands of South Australia, Austral. Ecol., 27, 422–432, https://doi.org/10.1046/j.1442-9993.2002.01196.x, 2002.
FAO, ITPS, GSBI, SCBD and EC: State of knowledge of soil biodiversity –
Status, challenges and potentialities, Report 2020, 2020.
Farji-Brener, A. G. and Werenkraut, V.: The effects of ant nests on soil fertility and plant performance: a meta-analysis, J. Anim. Ecol., 86, 866–877, https://doi.org/10.1111/1365-2656.12672, 2017.
Ferreira, A. C., Nobre, M. F., Moore, E., Rainey, F. A., Battista, J. R., and Da Costa, M. S.: Characterization and radiation resistance of new isolates of Rubrobacter radiotolerans and Rubrobacter xylanophilus, Extremophiles, 3, 235–238, https://doi.org/10.1007/s007920050121, 1999.
Filser, J., Faber, J. H., Tiunov, A. V., Brussaard, L., Frouz, J., De Deyn, G., Uvarov, A. V., Berg, M. P., Lavelle, P., Loreau, M., Wall, D. H., Querner, P., Eijsackers, H., and Jiménez, J. J.: Soil fauna: key to new carbon models, SOIL, 2, 565–582, https://doi.org/10.5194/soil-2-565-2016, 2016.
Folgarait, P.: Ant biodiversity to ecosystem functioning: a review, Biodivers. Conserv., 7, 1121–1244, https://doi.org/10.1023/A:1008891901953, 1998.
Frouz, J., Holec, M., and Kalčík, J.: The effect of Lasius niger (Hymenoptera, Formicidae) ant nest on selected soil chemical properties, Pedobiologia, 47, 205–212, https://doi.org/10.1078/0031-4056-00184, 2003.
Galloway, J. N., Dentener, F. J., Capone, D. G., Boyer, E. W., Howarth, R. W., Seitzinger, S. P., Asner, G. P., Cleveland, C. C., Green, P. A., Holland, E. A., Karl, D. M., Michaels, A. F., Porter, J. H., Townsend, A. R., and Vörösmarty, C. J.: Nitrogen cycles: past, present, and future, Biogeochemistry, 70, 153–226, 2004.
Gilad, E., von Hardenberg, J., Provenzale, A., Shachak, M., and Meron, E.: Ecosystem Engineers: From Pattern Formation to Habitat Creation, Phys. Rev. Lett., 93, 098105, https://doi.org/10.1103/PhysRevLett.93.098105, 2004.
Ginzburg, O., Whitford, W. G., and Steinberger, Y.: Effects of harvester ant (Messor spp.) activity on soil properties and microbial communities in a Negev Desert ecosystem, Biol. Fert. Soils, 45, 165–173, https://doi.org/10.1007/s00374-008-0309-z, 2008.
Gosselin, E. N., Holbrook, J. D., Huggler, K., Brown, E., Vierling, K. T., Arkle, R. S., and Pilliod, D. S.: Ecosystem engineering of harvester ants: effects on vegetation in a sagebrush-steppe ecosystem, West. N. Am. Naturalist, 76, 82–89, https://doi.org/10.3398/064.076.0109, 2016.
Greening, C., Biswas, A., Carere, C. R., Jackson, C. J., Taylor, M. C., Stott, M. B., Cook, G. M., and Morales, S. E.: Genomic and metagenomic surveys of hydrogenase distribution indicate H2 is a widely utilised energy source for microbial growth and survival, ISME J., 10, 761–777, https://doi.org/10.1038/ismej.2015.153, 2016.
Hansen, B. B., Henriksen, S., Aanes, R., and Sæther, B. E.: Ungulate impact on vegetation in a two-level trophic system, Polar Biol., 30, 549–558, https://doi.org/10.1007/s00300-006-0212-8, 2007.
Henrikus, S. S., Wood, E. A., McDonald, J. P., Cox, M. M., Woodgate, R., Goodman, M. F., van Oijen, A. M., and Robinson, A.: DNA polymerase IV primarily operates outside of DNA replication forks in Escherichia coli, PLoS Genet., 14, 1–29, https://doi.org/10.1371/journal.pgen.1007161, 2018.
Iwai, S., Weinmaier, T., Schmidt, B. L., Albertson, D. G., Poloso, N. J., Dabbagh, K., and DeSantis, T. Z.: Piphillin: Improved prediction of metagenomic content by direct inference from human microbiomes, PLoS One, 11, 1–18, https://doi.org/10.1371/journal.pone.0166104, 2016.
Jones, C. G., Lawton, J. H., and Shachak, M.: Organisms as Ecosystem Engineers, Oikos, 69, 373–386, 1994.
Kaneshisa, M. and Goto, S.: KEGG: Kyoto Encyclopedia of Genes and Genomes,
Nucleic Acids Res., 28, 27–30, https://doi.org/10.1093/nar/28.1.27,
2000.
Kidron, G. J.: The effect of shrub canopy upon surface temperatures and evaporation in the Negev Desert, Earth Surf. Proc. Land., 34, 123–132, 2009.
Klindworth, A., Pruesse, E., Schweer, T., Peplies, J., Quast, C., Horn, M., Glöckner, F. O., and Glockner, F. O.: Evaluation of general 16S ribosomal RNA gene PCR primers for classical and next-generation sequencing-based diversity studies, Nucleic Acids Res., 41, 1–11, https://doi.org/10.1093/nar/gks808, 2013.
Kruskal, W. H. and Wallis, W. A.: Use of Ranks in One-Criterion Variance Analysis, J. Am. Stat. Assoc., 47, 583–621, https://doi.org/10.1080/01621459.1952.10483441, 1952.
Lavelle, P.: Functional domains in soils, Ecol. Res., 17, 441–450, https://doi.org/10.1046/j.1440-1703.2002.00509.x, 2002.
Lavelle, P., Blanchart, E., Martin, A., Spain, A. V., and Martin, S.: Impact
of Soil Fauna on the Properties of Soils in the Humid Tropics, in: SSSA Spec. Publ., Vol. 29, https://doi.org/10.2136/sssaspecpub29.c9, 1992.
Lavelle, P., Decaëns, T., Aubert, M., Barot, S., Blouin, M., Bureau, F.,
Margerie, P., Mora, P., and Rossi, J. P.: Soil invertebrates and ecosystem
services, Eur. J. Soil Biol., 42, Suppl. 1, https://doi.org/10.1016/j.ejsobi.2006.10.002, 2006.
Lennon, J. T. and Jones, S. E.: Microbial seed banks: The ecological and evolutionary implications of dormancy, Nat. Rev. Microbiol., 9, 119–130, https://doi.org/10.1038/nrmicro2504, 2011.
León-Sobrino, C., Ramond, J. B., Maggs-Kölling, G., and Cowan, D. A.: Nutrient acquisition, rather than stress response over diel cycles, drives microbial transcription in a hyper-arid Namib desert soil, Front. Microbiol., 10, 1–11, https://doi.org/10.3389/fmicb.2019.01054, 2019.
MacMahon, J. A., Mull, J. F., and Crist, T. O.: Harvester ants (Pogonomyrmex spp.): their community and ecosystem influences, Annu. Rev. Ecol. Syst., 31, 265–291, https://doi.org/10.1146/annurev.ecolsys.31.1.265, 2000.
McMurdie, P. J., Holmes, S., Jordan, G., and Chamberlain, S.: Phyloseq: handling and analysis of high-throughput microbiome census data, 2017.
Meier, D. V., Imminger, S., Gillor, O., and Woebken, D.: Distribution of Mixotrophy and Desiccation Survival Mechanisms across Microbial Genomes in an Arid Biological Soil Crust Community, mSystems, 6, 1–20, https://doi.org/10.1128/msystems.00786-20, 2021.
Narayan, N. R., Weinmaier, T., Laserna-Mendieta, E. J., Claesson, M. J., Shanahan, F., Dabbagh, K., Iwai, S., and Desantis, T. Z.: Piphillin predicts metagenomic composition and dynamics from DADA2- corrected 16S rDNA sequences, BMC Genomics, 21, 1–12, https://doi.org/10.1186/s12864-020-6537-9, 2020.
Oksanen, J., Blanchet, F. G., Kindt, R., Legen-, P., Minchin, P. R., Hara, R. B. O., Simpson, G. L., Solymos, P., and Stevens, M. H. H.: Package “vegan”, ISBN 0-387-95457-0, 2014.
Oren, Y., Perevolotsky, A., Brand, S., and Shachak, M.: Livestock and
engineering network in the Israeli Negev: Implications for ecosystem
management, in: Ecosystem Engineers, Vol. 4, Elsevier Inc., 323–342,
2007.
Pariente, S.: Spatial patterns of soil moisture as affected by shrubs, in different climatic conditions, Environ. Monit. Assess., 73, 237–251, https://doi.org/10.1023/A:1013119405441, 2002.
Passarelli, C., Olivier, F., Paterson, D. M., Meziane, T., and Hubas, C.: Organisms as cooperative ecosystem engineers in intertidal flats, J. Sea Res., 92, 92–101, https://doi.org/10.1016/j.seares.2013.07.010, 2014.
Preiss, J.: Bacterial glycogen synthesis and its regulation, Annu. Rev. Microbiol., 38, 419–458, 1984.
Preiss, J. and Sivak, M.: 3.14 – Starch and Glycogen Biosynthesis, edited
by: Barton, S. D., Nakanishi, K., and Meth-Cohn, O. B. T., Pergamon, Oxford, 441–495, 1999.
Prieur, D.: An Extreme Environment on Earth: Deep-Sea Hydrothermal Vents. Lessons for Exploration of Mars and Europa, in: Lectures in Astrobiology: Volume II, edited by: Gargaud, M., Martin, H., and Claeys, P., Springer, Berlin, Heidelberg, 319–345, 2007.
Quast, C., Pruesse, E., Yilmaz, P., Gerken, J., Schweer, T., Yarza, P., Peplies, J., and Glöckner, F. O.: The SILVA ribosomal RNA gene database project: improved data processing and web-based tools, Nucleic Acids Res., 41, D590–D596, https://doi.org/10.1093/nar/gks1219, 2013.
R Core Team, I.: R: A language and environment for statistical computing, 2016.
Rajeev, L., Da Rocha, U. N., Klitgord, N., Luning, E. G., Fortney, J., Axen, S. D., Shih, P. M., Bouskill, N. J., Bowen, B. P., Kerfeld, C. A., Garcia-Pichel, F., Brodie, E. L., Northen, T. R., and Mukhopadhyay, A.: Dynamic cyanobacterial response to hydration and dehydration in a desert biological soil crust, ISME J., 7, 2178–2191, https://doi.org/10.1038/ismej.2013.83, 2013.
Repar, J., Briski, N., Buljubašić, M., Zahradka, K., and Zahradka, D.: Exonuclease VII is involved in “reckless” DNA degradation in UV-irradiated Escherichia coli, Mutat. Res., 750, 96–104, https://doi.org/10.1016/j.mrgentox.2012.10.005, 2012.
Saul-Tcherkas, V. and Steinberger, Y.: Soil microbial diversity in the vicinity of a Negev desert shrub-Reaumuria negevensis, Microb. Ecol., 61, 64–81, https://doi.org/10.1007/s00248-010-9763-x, 2011.
Schlesinger, W. H. and Pilmanis, A. M.: Plant-soil interactions in deserts, Biogeochemistry, 42, 169–187, 1998.
Schlesinger, W. H., Raikks, J. A., Hartley, A. E., and Cross, A. F.: On the spatial pattern of soil nutrients in desert ecosystems, Ecology, 77, 364–374, https://doi.org/10.2307/2265615, 1996.
Schulze-Makuch, D., Wagner, D., Kounaves, S. P., Mangelsdorf, K., Devine, K. G., de Vera, J.-P., Schmitt-Kopplin, P., Grossart, H.-P., Parro, V., Kaupenjohann, M., Galy, A., Schneider, B., Airo, A., Frösler, J., Davila, A. F., Arens, F. L., Cáceres, L., Cornejo, F. S., Carrizo, D., Dartnell, L., DiRuggiero, J., Flury, M., Ganzert, L., Gessner, M. O., Grathwohl, P., Guan, L., Heinz, J., Hess, M., Keppler, F., Maus, D., McKay, C. P., Meckenstock, R. U., Montgomery, W., Oberlin, E. A., Probst, A. J., Sáenz, J. S., Sattler, T., Schirmack, J., Sephton, M. A., Schloter, M., Uhl, J., Valenzuela, B., Vestergaard, G., Wörmer, L., and Zamorano, P.: Transitory microbial habitat in the hyperarid Atacama Desert, P. Natl. Acad. Sci. USA, 115, 2670–2675, https://doi.org/10.1073/pnas.1714341115, 2018.
Segoli, M., Ungar, E. D., and Shachak, M.: Shrubs enhance resilience of a
semi-arid ecosystem by engineering and regrowth, Ecohydrology, 1, 330–339, 2008.
Segoli, M., Ungar, E. D., Giladi, I., Arnon, A., and Shachak, M.: Untangling the positive and negative effects of shrubs on herbaceous vegetation in drylands, Landscape Ecol., 27, 899–910, https://doi.org/10.1007/s10980-012-9736-1, 2012.
Shachak, M., Boeken, B., Groner, E., Kadmon, R., Lubin, Y., Meron, E., Ne'eman, G., Perevolotsky, A., Shkedy, Y., and Ungar, E. D.: Woody species as landscape modulators and their effect on biodiversity patterns, Bioscience, 58, 209–221, https://doi.org/10.1641/B580307, 2008.
Sklarz, M. Y., Levin, L., Gordon, M., and Chalifa-Caspi, V.: NeatSeq-Flow: A Lightweight High Throughput Sequencing Workflow Platform for Non-Programmers and Programmers alike, bioRxiv, 173005, https://doi.org/10.1101/173005, 2018.
Slade, D. and Radman, M.: Oxidative Stress Resistance in Deinococcus radiodurans, Microbiol. Mol. Biol. R.,75, 133–191, https://doi.org/10.1128/mmbr.00015-10, 2011.
SSSA: Methods of Soil Analysis: Part 3 Chemical methods, 5.3, edited by: Sparks, D. L., Page, A. L., A, H. P., Loeppert, R. H., Soltanpour, P. N., Tabatabai, M. A., Johnson, C. T., and Sumner, M. E., 1390 pp., 1996.
Steven, B., Gallegos-Graves, L. V., Yeager, C., Belnap, J., and Kuske, C. R.: Common and distinguishing features of the bacterial and fungal communities in biological soil crusts and shrub root zone soils, Soil Biol. Biochem., 69, 302–312, https://doi.org/10.1016/J.SOILBIO.2013.11.008, 2014.
Tveit, A. T., Hestnes, A. G., Robinson, S. L., Schintlmeister, A., Dedysh, S. N., Jehmlich, N., Von Bergen, M., Herbold, C., Wagner, M., Richter, A., and Svenning, M. M.: Widespread soil bacterium that oxidizes atmospheric methane, P. Natl. Acad. Sci. USA, 116, 8515–8524, https://doi.org/10.1073/pnas.1817812116, 2019.
Vonshak, A., Sklarz, M. Y., Hirsch, A. M., and Gillor, O.: Perennials but not slope aspect affect the diversity of soil bacterial communities in the northern Negev Desert, Israel, Soil Res., 56, 123–128, https://doi.org/10.1071/SR17010, 2018.
Wagner, D.: The Influence of Ant Nests on Acacia Seed Production, Herbivory and Soil Nutrients, J. Ecol., 85, 83–93, https://doi.org/10.2307/2960629, 1997.
Wagner, D. and Jones, J. B.: The Contribution of Harvester Ant Nests, Pogonomyrmex rugosus (Hymenoptera, Formicidae), to Soil Nutrient Stocks and Microbial Biomass in the Mojave Desert, Environ. Entomol., 33, 599–607, https://doi.org/10.1603/0046-225X-33.3.599, 2004.
Walker, L. R., Thompson, D. B., and Landau, F. H.: Experimental manipulations of fertile islands and nurse plant effects in the Mojave Desert, USA, West. N. Am. Naturalist, 61, 25–35, 2001.
West, N. E.: Nutrient cycling in desert ecosystems, in: Arid land ecosystems,
Vol. 2, Structure, functioning and management, edited by: Goodall, D. W., Perry, R. A., and Howes, K. M. W., Cambridge University Press, Cabridge, UK, ISBN: 9780521229883, 301–324, 1981.
Whitford, W. G. and Duval, B. D.: Ecology of Desert Systems, Academic Press Inc,
https://doi.org/10.1016/s0167-8809(02)00198-6,
2002.
Wickham, H.: Ggplot2: Elegant graphics for data analysis, 2016.
Wilby, A., Shachak, M., and Boeken, B.: Integration of ecosystem engineering and trophic effects of herbivores, Oikos, 92, 436–444, https://doi.org/10.1034/j.1600-0706.2001.920305.x, 2001.
Wright, J. P., Jones, C. G., Boeken, B., and Shachak, M.: Predictability of
ecosystem engineering effects on species richness across environmental
variability and spatial scales, Shrub mound effects on annual plant
diversity, J. Ecol., 94, 815–824, https://doi.org/10.1111/j.1365-2745.2006.01132.x, 2006.
Wright, S. F. and Upadhyaya, A.: Extraction of an abundant and unusual protein
from soil and comparison with hyphal protein of arbuscular mycorrhizal fungi,
Soil Sci., 161, 575–586, https://doi.org/10.1097/00010694-199609000-00003, 1996.
Short summary
In this paper, we describe changes in desert soil bacterial diversity and function when two ecosystem engineers, shrubs and ant nests, in an arid environment are present. The results show that bacterial activity increases when there are ecosystem engineers and that their impact is non-additive. This is one of a handful of studies that investigated the separate and combined effects of ecosystem engineers on soil bacterial communities investigating both composition and function.
In this paper, we describe changes in desert soil bacterial diversity and function when two...