Abstract
Background and aims
We lack studies evaluating how the identity of plant, lichen and moss species relates to microbial abundance and soil functioning on Antarctica. If species identity is associated with soil functioning, distributional changes of key species, linked to climate change, could significantly affect Antarctic soil functioning.
Methods
We evaluated how the identity of six Antarctic plant, lichen and moss species relate to a range of soil attributes (C, N and P cycling), microbial abundance and structure in Livingston Island, Maritime Antarctica. We used an effect size metric to predict the association between species (vs. bare soil) and the measured soil attributes.
Results
We observed species-specific effects of the plant and biocrust species on soil attributes and microbial abundance. Phenols, phosphatase and β-D-cellobiosidase activities were the most important attributes characterizing the observed patterns. We found that the evaluated species positively correlated with soil nutrient availability and microbial abundance vs. bare soil.
Conclusions
We provide evidence, from a comparative study, that plant and biocrust identity is associated with different levels of soil functioning and microbial abundance in Maritime Antarctica. Our results suggest that changes in the spatial distribution of these species linked to climate change could potentially entail changes in the functioning of Antarctic terrestrial ecosystems.
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References
Agati G, Tattini M (2010) Multiple functional roles of flavonoids in photoprotection. New Phytol 186:786–793. https://doi.org/10.1111/j.1469-8137.2010.03269.x
Allington GRH, Valone TJ (2014) Islands of fertility: a byproduct of grazing? Ecosystems 17:127–141. https://doi.org/10.1007/s10021-013-9711-y
Almeida ICC, Schaefer CEGR, Fernandes RBA, Pereira TTC, Nieuwendam A, Pereira AB (2014) Active layer thermal regime at different vegetation covers at lions rump, king George Island, maritime Antarctica. Geomorphology 225:36–46. https://doi.org/10.1016/j.geomorph.2014.03.048
Amesbury MJ, Roland TP, Royles J, Hodgson DA, Convey P, Griffiths H, Charman DJ (2017) Widespread biological response to rapid warming on the Antarctic peninsula. Curr Biol 27:1616–1622.e2. https://doi.org/10.1016/j.cub.2017.04.034
Anderson MJ (2001) A new method for non-parametric multivariate analysis of variance. Austral Ecol 26:32–46. https://doi.org/10.1111/j.1442-9993.2001.01070.pp.x
Anderson JM, Ingram JSI (1993) Tropical soil biology and fertility: a handbook of methods. Wallingford:CABI
Archer E (2013) Estimate permutation p-values for importance metrics. R package version 1.5.2
Armas C, Ordiales R, Pugnaire FICN (2004) Measuring plant interactions: a new comarative index. Ecology 85(10):2682–2686. https://doi.org/10.1890/03-0650
Arnosti C, Bell C, Moorhead DL, Sinsabaugh RL, Steen AD, Stromberger M, Wallenstein M, Weintraub MN (2014) Extracellular enzymes in terrestrial, freshwater, and marine environments: perspectives on system variability and common research needs. Biogeochemistry 117:5–21. https://doi.org/10.1007/s10533-013-9906-5
Baker NR, Allison SD (2017) Extracellular enzyme kinetics and thermodynamics along a climate gradient in southern California. Soil Biol Biochem 114:82–92. https://doi.org/10.1016/j.soilbio.2017.07.005
Bañón M, Justel A, Velázquez D, Quesada A (2013) Regional weather survey on byers peninsula, Livingston Island, south Shetland Islands, Antarctica. Antarct Sci 25:146–156. https://doi.org/10.1017/S0954102012001046
Barger NN, Weber B, Garcia-Pichel F, et al (2016) Patterns and Controls on Nitrogen Cycling of Biological Soil Crusts. In: Weber B, Büdel B, Belnap J (eds) Biological Soil Crusts: An Organizing Principle in Drylands. Springer International Publishing, Cham, pp 257–285
Bates ST, Nash TH, Sweat KG, Garcia-Pichel F (2010) Fungal communities of lichen-dominated biological soil crusts: diversity, relative microbial biomass, and their relationship to disturbance and crust cover. J Arid Environ 74:1192–1199. https://doi.org/10.1016/j.jaridenv.2010.05.033
Bell CW, Fricks BE, Rocca JD, Steinweg JM, McMahon SK, Wallenstein MD (2013) High-throughput Fluorometric measurement of potential soil extracellular enzyme activities. J Vis Exp:1–16. https://doi.org/10.3791/50961
Bell C, Carrillo Y, Boot CM, Rocca JD, Pendall E, Wallenstein MD (2014a) Rhizosphere stoichiometry: are C : N : P ratios of plants, soils, and enzymes conserved at the plant species-level? New Phytol 201:505–517. https://doi.org/10.1111/nph.12531
Bell C, Stromberger M, Wallenstein M (2014b) New insights into enzymes in the environment. Biogeochemistry 117:1–4. https://doi.org/10.1007/s10533-013-9935-0
Belnap J (2006) The potential roles of biological soil crusts in dryland hydrologic cycles. Hydrol Process 20:3159–3178. https://doi.org/10.1002/hyp.6325
Belnap J (2011) Biological phosphorus cycling in Dryland regions. In: Bünemann E, Oberson A, Frossard E (eds) Phosphorus in action. Springer Berlin Heidelberg, pp 371–406
Belnap J, Prasse R, Harper KT (2003) Influence of biological soil crusts on soil environments and vascular plants. In: Belnap J, Lange OL (eds) Biological soil crusts: structure, function, and management. Springer Berlin Heidelberg, Berlin, Heidelberg, pp 281–300
Bergstrom DM, Convey P, Huiskes AHL (2006) Trends in Antarctic Terrestrial and Limnetic Trends in Antarctic Terrestrial and Limnetic
Beyer L, Pingpank K, Wriedt G, Bölter M (2000) Soil formation in coastal continental Antarctica (Wilkes land). Geoderma 95:283–304. https://doi.org/10.1016/S0016-7061(99)00095-6
Bowker MA, Mau RL, Maestre FT, Escolar C, Castillo-Monroy AP (2011) Functional profiles reveal unique ecological roles of various biological soil crust organisms. Funct Ecol 25:787–795. https://doi.org/10.1111/j.1365-2435.2011.01835.x
Bray RH, Kurtz LT (1945) Determination of Total, organic, and available forms of phosphorus in soils. Soil Sci 59:39–46
Breiman L (2001) Random forests. Mach Learn 45:5–32. https://doi.org/10.1186/1478-7954-9-29
Brookes P, Landman A, Pruden G (1985) Chloroform fumigation and the release of soil nitrogen: a rapid direct extraction method to measure microbial biomass nitrogen in soil. Soil Biol 17:837–842
Burns RG, DeForest JL, Marxsen J et al (2013) Soil enzymes in a changing environment: current knowledge and future directions. Soil Biol Biochem 58:216–234. https://doi.org/10.1016/j.soilbio.2012.11.009
Cannone N, Guglielmin M (2010) Relationships between periglacial features and vegetation development in Victoria Land, continental Antarctica. 22:703–713. doi: https://doi.org/10.1017/S0954102010000751
Cannone N, Wagner D, Hubberten HW, Guglielmin M (2008) Biotic and abiotic factors influencing soil properties across a latitudinal gradient in Victoria land, Antarctica. Geoderma 144:50–65. https://doi.org/10.1016/j.geoderma.2007.10.008
Cannone N, Guglielmin M, Convey P, Worland MR, Favero Longo SE (2016) Vascular plant changes in extreme environments: effects of multiple drivers. Clim Chang 134:651–665. https://doi.org/10.1007/s10584-015-1551-7
Celenza G, Segatore B, Setacci D, Bellio P, Brisdelli F, Piovano M, Garbarino JA, Nicoletti M, Perilli M, Amicosante G (2012) In vitro antimicrobial activity of pannarin alone and in combination with antibiotics against methicillin-resistant Staphylococcus aureus clinical isolates. Phytomedicine 19:596–602. https://doi.org/10.1016/j.phymed.2012.02.010
Celenza G, Segatore B, Setacci D, Perilli M, Brisdelli F, Bellio P, Piovano M, Garbarino JA, Amicosante G, Nicoletti M (2013) Antibacterial activity of selected metabolites from Chilean lichen species against methicillin-resistant staphylococci. Nat Prod Res 27:1528–1531. https://doi.org/10.1080/14786419.2012.730043
Cesco S, Neumann G, Tomasi N, Pinton R, Weisskopf L (2010) Release of plant-borne flavonoids into the rhizosphere and their role in plant nutrition. Plant Soil 329:1–25. https://doi.org/10.1007/s11104-009-0266-9
Chapman SK, J a L, Hart SC, Koch GW (2005) Plants actively control nitrogen cycling: uncorking the microbail bottleneck. New Phytol 169:27–34. https://doi.org/10.1111/j.1469-8137.2005.01571.x
Chen J, Stark JM (2000) Plant species e € ects and carbon and nitrogen cycling in a sagebrush ± crested wheatgrass soil. 32:47–57
Cleveland CC, Reed SC, Keller AB, Nemergut DR, O’Neill SP, Ostertag R, Vitousek PM (2014) Litter quality versus soil microbial community controls over decomposition: a quantitative analysis. Oecologia 174:283–294. https://doi.org/10.1007/s00442-013-2758-9
Colesie C, Büdel B, Hurry V, Green TGA (2017) Can Antarctic lichens acclimatize to changes in temperature? Glob Chang Biol 24:1123–1135. https://doi.org/10.1111/gcb.13984
Concostrina-Zubiri L, Huber-Sannwald E, Martínez I, Flores Flores JL, Escudero A (2013) Biological soil crusts greatly contribute to small-scale soil heterogeneity along a grazing gradient. Soil Biol Biochem 64:28–36. https://doi.org/10.1016/j.soilbio.2013.03.029
Cornelissen JHC, Lang SI, Soudzilovskaia NA, During HJ (2007) Comparative cryptogam ecology: a review of bryophyte and lichen traits that drive biogeochemistry. Ann Bot 99:987–1001. https://doi.org/10.1093/aob/mcm030
Crittenden PD (1999) Aspects of the ecology of mat-forming lichens. Rangifer 20:127–139
Cross AF, Schlesinger WH (1999) Plant regulation of soil nutrient distribution in the northern Chihuahuan Desert. Plant Ecol 145:11–25
De Albuquerque MP, de Victoria FC, Schünemann AL et al (2012) Plant composition of Skuas nests at Hennequin point, king George Island, Antarctica. Am J Plant Sci 3:688–692. https://doi.org/10.4236/ajps.2012.35082
de Graaff MA, Throop HL, Verburg PSJ, Arnone JA, Campos X (2014) A synthesis of climate and vegetation cover effects on biogeochemical cycling in shrub-dominated Drylands. Ecosystems 17:931–945. https://doi.org/10.1007/s10021-014-9764-6
Delgado-Baquerizo M, Covelo F, Gallardo A (2011) Dissolved organic nitrogen in Mediterranean ecosystems ∗ 1. Pedosph an. Int J 21:309–318. https://doi.org/10.1016/S1002-0160(11)60131-8
Delgado-Baquerizo M, Covelo F, Maestre FT, Gallardo A (2013) Biological soil crusts affect small-scale spatial patterns of inorganic N in a semiarid Mediterranean grassland. J Arid Environ 91:147–150. https://doi.org/10.1016/j.jaridenv.2013.01.005
Delgado-Baquerizo M, Gallardo A, Covelo F, Prado-Comesaña A, Ochoa V, Maestre FT (2015) Differences in thallus chemistry are related to species-specific effects of biocrust-forming lichens on soil nutrients and microbial communities. Funct Ecol 29:1087–1098. https://doi.org/10.1111/1365-2435.12403
Delgado-Baquerizo M, Maestre FT, Eldridge DJ, Bowker MA, Ochoa V, Gozalo B, Berdugo M, Val J, Singh BK (2016) Biocrust-forming mosses mitigate the negative impacts of increasing aridity on ecosystem multifunctionality in drylands. New Phytol 209:1540–1552. https://doi.org/10.1111/nph.13688
Dixon RA, Paiva NL (1995) Stress-induced Phenylpropanoid metabolism. Plant Cell 7:1085–1097. https://doi.org/10.2307/3870059
Escudero A, Giménez-Benavides L, Iriondo JM, Rubio A (2004) Patch dynamics and islands of fertility in a high mountain Mediterranean community. Arct Antarct Alp Res 36:518–527. https://doi.org/10.1657/1523-0430(2004)036[0518:PDAIOF]2.0.CO;2
Evans SE, Wallenstein MD (2012) Soil microbial community response to drying and rewetting stress: does historical precipitation regime matter? Biogeochemistry 109:101–116. https://doi.org/10.1007/s10533-011-9638-3
Fan F, Zhang F, Lu Y (2011) Linking plant identity and interspecific competition to soil nitrogen cycling through ammonia oxidizer communities. Soil Biol Biochem 43:46–54. https://doi.org/10.1016/j.soilbio.2010.09.009
Gianfreda L (2015) Enzymes of importance to rhizosphere processes. J Soil Sci Plant Nutr 15(2):283–306
Haigler CH, Weimer PJ (eds) (1991) Biosynthesis and biodegradation of cellulose. Marcel Dekker, New York, p 694. https://doi.org/10.1016/0307-4412(92)90135-9
Hauck M, Jürgens SR, Willenbruch K, Huneck S, Leuschner C (2009) Dissociation and metal-binding characteristics of yellow lichen substances suggest a relationship with site preferences of lichens. Ann Bot 103:13–22. https://doi.org/10.1093/aob/mcn202
Heritage J, Evans EGV, Killington RA (1999) The microbiology of soil and nutrient cycling. Microbiol Action:2–13
Hooper DU, Vitousek PM (1997) The effects of plant composition and diversity on ecosystem processes. Science (80-) 277:1302–1305
Hughes KA, Ott S, Bölter M, Convey P (2006) Colonisation processes. In: Trends in Antarctic terrestrial and limnetic ecosystems: Antarctica as a global indicator, pp 35–54
Iakiviak M, Mackie RI, Cann IKO (2011) Functional analyses of multiple lichenin-degrading enzymes from the rumen bacterium Ruminococcus albus 8. Appl Environ Microbiol 77:7541–7550. https://doi.org/10.1128/AEM.06088-11
Jax K (2010) Ecosystem functioning. Cambridge University Press, Cambridge
Jones DL, Oburger E (2011) Solubilization of phosphorus by soil microorganisms. In: Phosphorus in Action: Biological Processes in Soil Phosphorus Cycling pp 169–198
Jones D, Wilson M (1985) Chemical activity of lichens on mineral surfaces. A Rev Int Biodeterior 21:99–104
Kanda T, Yatomi H, Makishima S, Amano Y, Nisizawa K (1989) Substrate specificities of exo- and endo-type cellulases in the hydrolysis of β-(1→3)- and β-(1→4)-mixed D-glucans. J Biochem 105:127–132
Kappen L, Polarkologie I, Kiel U et al (1985) Vegetation and ecology of ice, free areas of northern Victoria land, Antarctica 2. Ecological conditions in typical microhabitats of lichens at birthday ridge. Polar Biol 4:213–225
Kardol P, Cregger MA, Campany CE, Classen AT (2010) Soil ecosystem functioning under climate change: plant species and community effects. Ecology 91:767–781. https://doi.org/10.1890/09-0135.1
Kennedy AD (1993) Water as a limiting factor in the Antarctic terrestrial environment: a biogeographical synthesis. Arct Alp Res 25:308–315. https://doi.org/10.2307/1551914
Kettler TA, Doran JW, Gilbert TL (2001) Simplified method for soil particle-size determination to accompany soil-quality analyses. Soil Sci Soc Am J 65:849–852. https://doi.org/10.2136/sssaj2001.653849x
Kirby KN, Gerlanc D (2013) BootES: an R package for bootstrap confidence intervals on effect sizes. Behav Res Methods 45:905–927. https://doi.org/10.3758/s13428-013-0330-5
Köhler H, Contreras RA, Pizarro M, Cortés-Antíquera R, Zúñiga GE (2017) Antioxidant responses induced by UVB radiation in Deschampsia antarctica Desv. Front Plant Sci 8:1–10. https://doi.org/10.3389/fpls.2017.00921
Kreyszig E (1978) Introductory Functional Analysis with Applications
Lawrey JD (1986) Biological role of lichen substances. Bryologist 89:111–122. https://doi.org/10.2307/3242751
Lawrey JD (1989) Lichen secondary compounds: evidence for a correspondence between Antiherbivore and antimicrobial function. Bryologist 92:326–328
Lee JR, Raymond B, Bracegirdle TJ, Chadès I, Fuller RA, Shaw JD, Terauds A (2017) Climate change drives expansion of Antarctic ice-free habitat. Nature 547:49–54. https://doi.org/10.1038/nature22996
Liu Y, Yang H, Li X, Xing Z (2014) Effects of biological soil crusts on soil enzyme activities in revegetated areas of the Tengger Desert, China. Appl Soil Ecol 80:6–14. https://doi.org/10.1016/j.apsoil.2014.03.015
Liu YR, Delgado-Baquerizo M, Trivedi P, He JZ, Singh BK (2016) Species identity of biocrust-forming lichens drives the response of soil nitrogen cycle to altered precipitation frequency and nitrogen amendment. Soil Biol Biochem 96:128–136. https://doi.org/10.1016/j.soilbio.2016.01.021
Liu YR, Delgado-Baquerizo M, Trivedi P, He JZ, Wang JT, Singh BK (2017) Identity of biocrust species and microbial communities drive the response of soil multifunctionality to simulated global change. Soil Biol Biochem 107:208–217. https://doi.org/10.1016/j.soilbio.2016.12.003
Maestre FT, Castillo-Monroy AP, Bowker MA, Ochoa-Hueso R (2012a) Species richness effects on ecosystem multifunctionality depend on evenness, composition and spatial pattern. J Ecol 100:317–330. https://doi.org/10.1111/j.1365-2745.2011.01918.x
Maestre FT, Quero JL, Gotelli NJ, Escudero A, Ochoa V, Delgado-Baquerizo M, Garcia-Gomez M, Bowker MA, Soliveres S, Escolar C, Garcia-Palacios P, Berdugo M, Valencia E, Gozalo B, Gallardo A, Aguilera L, Arredondo T, Blones J, Boeken B, Bran D, Conceicao AA, Cabrera O, Chaieb M, Derak M, Eldridge DJ, Espinosa CI, Florentino A, Gaitan J, Gatica MG, Ghiloufi W, Gomez-Gonzalez S, Gutierrez JR, Hernandez RM, Huang X, Huber-Sannwald E, Jankju M, Miriti M, Monerris J, Mau RL, Morici E, Naseri K, Ospina A, Polo V, Prina A, Pucheta E, Ramirez-Collantes DA, Romao R, Tighe M, Torres-Diaz C, Val J, Veiga JP, Wang D, Zaady E (2012b) Plant species richness and ecosystem multifunctionality in global Drylands. Science (80- ) 335:214–218. https://doi.org/10.1126/science.1215442
Malik AA, Chowdhury S, Schlager V, Oliver A, Puissant J, Vazquez PGM, Jehmlich N, von Bergen M, Griffiths RI, Gleixner G (2016) Soil fungal: bacterial ratios are linked to altered carbon cycling. Front Microbiol 7:1–11. https://doi.org/10.3389/fmicb.2016.01247
Mallen-Cooper M, Eldridge DJ (2016) Laboratory-based techniques for assessing the functional traits of biocrusts. Plant Soil 406:131–143. https://doi.org/10.1007/s11104-016-2870-9
Melick ADR, Seppelt RD (1997) Vegetation patterns in relation to climatic and endogenous changes in Wilkes land, continental Antarctica Source: The Journal of Ecology, Vol. 85, No. 1, ( Feb ., 1997 ), pp. 43–56 Published by : British Ecological Society Stable URL: http://www. J Ecol 85:43–56
Mihoč MAK, Giménez-Benavides L, Pescador DS, Sánchez AM, Cavieres LA, Escudero A (2016) Soil under nurse plants is always better than outside: a survey on soil amelioration by a complete guild of nurse plants across a long environmental gradient. Plant Soil 408:31–41. https://doi.org/10.1007/s11104-016-2908-z
Millbank JW (1978) The Contribution of nitrogen-fixing lichens to the nitrogen status of their environment. In: Environmental Role of Nitrogen-fixing Blue-green Algae and Asymbiotic Bacteria. p 260–?? (incomplete pages)
Millbank JW (1982) The assessment of nitrogen fixation and throughput by lichens: III. Losses of nitrogenous compounds by Peltigera Membranacea, P. Polydactyla and Lobaria Pulmonaria in simulated rainfall episodes. New Phytol 92:229–234. https://doi.org/10.1111/j.1469-8137.1982.tb03380.x
Miralles I, Domingo F, Cantón Y, Trasar-Cepeda C, Leirós MC, Gil-Sotres F (2012) Hydrolase enzyme activities in a successional gradient of biological soil crusts in arid and semi-arid zones. Soil Biol Biochem 53:124–132. https://doi.org/10.1016/j.soilbio.2012.05.016
Ochoa-Hueso R, Eldridge DJ, Delgado-Baquerizo M, Soliveres S, Bowker MA, Gross N, le Bagousse-Pinguet Y, Quero JL, García-Gómez M, Valencia E, Arredondo T, Beinticinco L, Bran D, Cea A, Coaguila D, Dougill AJ, Espinosa CI, Gaitán J, Guuroh RT, Guzman E, Gutiérrez JR, Hernández RM, Huber-Sannwald E, Jeffries T, Linstädter A, Mau RL, Monerris J, Prina A, Pucheta E, Stavi I, Thomas AD, Zaady E, Singh BK, Maestre FT (2018) Soil fungal abundance and plant functional traits drive fertile island formation in global drylands. J Ecol 106:242–253. https://doi.org/10.1111/1365-2745.12871
Otálora MAG, Jørgensen PM, Wedin M (2014) A revised generic classification of the jelly lichens, Collemataceae. Fungal Divers 64:275–293. https://doi.org/10.1007/s13225-013-0266-1
Parnikoza I, Dykyy I, Ivanets V, Kozeretska I, Kunakh V, Rozhok A, Ochyra R, Convey P (2012) Use of Deschampsia antarctica for nest building by the kelp gull in the argentine islands area (maritime Antarctica) and its possible role in plant dispersal. Polar Biol 35:1753–1758. https://doi.org/10.1007/s00300-012-1212-5
Perroni-Ventura Y, Montaña C, García-Oliva F (2010) Carbon-nitrogen interactions in fertility island soil from a tropical semi-arid ecosystem. Funct Ecol 24:233–242. https://doi.org/10.1111/j.1365-2435.2009.01610.x
Qu XH, Wang JG (2008) Effect of amendments with different phenolic acids on soil microbial biomass, activity, and community diversity. Appl Soil Ecol 39:172–179. https://doi.org/10.1016/j.apsoil.2007.12.007
Rai AN, Bergman B, Rasmussen U (eds) (2002) Cyanobacteria in Symbiosis. Springer Netherlands, Dordrecht. https://doi.org/10.1007/0-306-48005-0
Reiss J, Bridle JR, Montoya JM, Woodward G (2009) Emerging horizons in biodiversity and ecosystem functioning research. Trends Ecol Evol 24:505–514. https://doi.org/10.1016/j.tree.2009.03.018
Ruhland CT, Xiong FS, Clark WD, Day TA (2005) The influence of ultraviolet-B radiation on growth, Hydroxycinnamic acids and flavonoids of Deschampsia antarcfica during springtime ozone depletion in Antarctica. Photochem Photobiol 81:1086–1093. https://doi.org/10.1562/2004-09-18-RA-321
Sancho LG, Schulz F, Schroeter B, Kappen L (1999) Bryophyte and lichen flora of South Bay (Livingston Island: south Shetland Islands, Antarctica). Nova Hedwigia 68:301–337
Sancho LG, Belnap J, Colesie C, et al (2016) Carbon Budgets of Biological Soil Crusts at Micro-, Meso-, and Global Scales. In: Weber B, Büdel B, Belnap J (eds) Biological Soil Crusts: An Organizing Principle in Drylands. Springer International Publishing, Cham, pp 287–304
Sancho LG, Pintado A, Navarro F, Ramos M, de Pablo MA, Blanquer JM, Raggio J, Valladares F, Green TGA (2017) Recent warming and cooling in the Antarctic peninsula region has rapid and large effects on lichen vegetation. Sci Rep 7:5689. https://doi.org/10.1038/s41598-017-05989-4
Schlensog M, Green TGA, Schroeter B (2013) Life form and water source interact to determine active time and environment in cryptogams: an example from the maritime Antarctic. Oecologia 173:59–72. https://doi.org/10.1007/s00442-013-2608-9
Schlesinger WH, Reynolds JF, Cunningham GL, Huenneke LF, Jarrell WM, Virginia RA, Whitford WG (1990) Biological feedbacks in global desertification. Science (80-) 247:1043–1048. https://doi.org/10.1126/science.247.4946.1043
Schlesinger WH, Raikes JA, Hartley AE, Cross AF (1996) On the spatial pattern of soil nutrients in desert ecosystems. Ecology 77:364–374
Schroeter B, Green TGA, Pannewitz S, Schlensog M, Sancho LG (2011) Summer variability, winter dormancy: lichen activity over 3 years at Botany Bay, 77°S latitude, continental Antarctica. Polar Biol 34:13–22. https://doi.org/10.1007/s00300-010-0851-7
Søchting U, Øvstedal D, Sancho LG (2004) The lichens of Hurd peninsula, Livingston Island, south Shetlands. Antarctica Biblioth Lichenol:607–658
Solomon S (1999) Stratospheric ozone depletion: A review of concepts and history. 275–316
Solomon S (2004) The hole truth. Nature 427:289–291. https://doi.org/10.1038/427289a
Torres-Mellado GA, Jaña R, Casanova-Katny MA (2011) Antarctic hairgrass expansion in the south Shetland archipelago and Antarctic peninsula revisited. Polar Biol 34:1679–1688. https://doi.org/10.1007/s00300-011-1099-6
van der Putten WH, Bradford MA, Pernilla Brinkman E, van de Voorde TFJ, Veen GF (2016) Where, when and how plant–soil feedback matters in a changing world. Funct Ecol 30:1109–1121. https://doi.org/10.1111/1365-2435.12657
Vieira G, Mora C, Pina P, Schaefer CER (2014) A proxy for snow cover and winter ground surface cooling: mapping Usnea sp. communities using high resolution remote sensing imagery (maritime Antarctica). Geomorphology 225:69–75. doi: https://doi.org/10.1016/j.geomorph.2014.03.049
Vitousek PM, Cassman K, Cleveland C, Crews T, Field CB, Grimm NB, Howarth RW, Marino R, Martinelli L, Rastetter EB, Sprent JI (2002) Towards an ecological understanding of biological nitrogen fixation. Biogeochemistry 57:1–45
Wasley J, Robinson SA, Lovelock CE, Popp M (2006) Climate change manipulations show Antarctic flora is more strongly affected by elevated nutrients than water. Glob Chang Biol 12:1800–1812. https://doi.org/10.1111/j.1365-2486.2006.01209.x
Whitton B, Al-Shehri AM, Ellwood NTW, Turner BL (2005) Ecological aspects of phosphatase activity in cyanobacteria, eukaryotic algae and bryophytes. Org Phosphorus Environ:1–43
Xiong FS, Day TA (2001) Effect of solar ultraviolet-B radiation during springtime ozone depletion on photosynthesis and biomass production of Antarctic vascular plants. Plant Physiol 125:738–751. https://doi.org/10.1104/pp.125.2.738
Zhang W, Zhang G, Liu G, Dong Z, Chen T, Zhang M, Dyson PJ, An L (2012) Bacterial diversity and distribution in the southeast edge of the Tengger Desert and their correlation with soil enzyme activities. J Environ Sci (China) 24:2004–2011. https://doi.org/10.1016/S1001-0742(11)61037-1
Acknowledgements
We thank the reviewers and editor of this article for their constructive and precise comments. We also thank Victoria Ochoa, Beatriz Gozalo and Chanda Trivedi for their kind assistance through laboratory work and Jasmine Grinyer for revising the English of this manuscript. We thank José Manuel Blanquer, the B.I.O. Hesperides crew and the Spanish Antarctic Base JCI team for their support during the field campaign. This research was supported by grants from the Spanish Ministerio de Economía y Competitividad (CTM2015-64728-C2-1-R, CTM2012-38222-CO2-01 and CGL2013-44661-R) and the European Research Council (BIODESERT project, ERC Grant agreement n° 647038). ABG was supported by FPI (BES-2013-062945) and short stay (EEBB-I-15-09187) grants from Spanish Ministerio de Economía y Competitividad. MDB is supported from the Marie Sklodowska-Curie Actions of the Horizon 2020 Framework Program H2020-MSCA-IF-2016 under REA grant agreement n° 702057 and from the BES (MUSGONET) grant agreement n° LRA17\1193. BKS work is supported by the Australian Research Council (DP170104634).
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Figure S1
Fertility effect of the species studied (vs. bare ground areas), as measured with the relative interaction index (RII), on soil variables that did not show statistical differences between species (n = 10, except Cladonia sp. with n = 6). CL: Cladonia sp.; DA: Deschampsia antarctica; LP: Leptogium puberulum; SA: Stereocaulon alpinum; SG: Sphaerophorus globosus; SU: Sanionia uncinata. (PNG 120 kb)
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Benavent-González, A., Delgado-Baquerizo, M., Fernández-Brun, L. et al. Identity of plant, lichen and moss species connects with microbial abundance and soil functioning in maritime Antarctica. Plant Soil 429, 35–52 (2018). https://doi.org/10.1007/s11104-018-3721-7
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DOI: https://doi.org/10.1007/s11104-018-3721-7