BIOLOGICAL SOIL CRUSTS CONTROL N DYNAMICS AND MICROBIAL FUNCTIONAL DIVERSITY IN RESPONSE TO NUTRIENT ADDITIONS Manuel Delgado-Baquerizo (mdelbaq@upo.es)1, Lourdes Morillas (lmorvin@upo.es)1, Fernando T. Maestre (fernando.maestre@urjc.es)2 & Antonio Gallardo (agallardo@upo.es)1. 1 Área de ecología, Departamento de Sistemas Físicos, Químicos y Naturales, Universidad Pablo de Olavide, Carretera de Utrera km. 1, 41013 Sevilla, Spain. 2 Área de Biodiversidad y Conservación, Departamento de Biología y Geología, Escuela Superior de Ciencias Experimentales y Tecnología, Universidad Rey Juan Carlos, 28933 Móstoles, Spain INTRODUCTION STUDY SITE AND SAMPLING DESIGN Human activities are changing carbon (C), nitrogen (N), and phosphorus (P) ratios in soil ecosystems 1. This study was conducted in a semi-arid grassland at the Aranjuez experimental station (Fig 1). Soil sampling was carried at Spring (2010). Five soil samples (top 4 cm) were taken under two microsites: bare soil (BS) and BSC (Fig 1). In drylands, biological soil crusts (BSCs) play a prevalent role in the Nitrogen (N) cycle 2-3, however its influence on the phosphorus (P) cycle is poorly known. We evaluated how BSCs and different N, C and P ratios affect to the N dynamics and microbial functional diversity Soil were incubated using different N (100 mg N kg-1), C (2.323 mg C kg-1) and P (20 mg P kg-1) treatments (Control, N, C, P, C+N, N+P, C+P, and C+N+P)4 at 20ºC during 2 different incubation periods (1-week and 3-week) in a factorial design. LAB ANALISYS A B The functional diversity of soil heterotrophic microbial communities was analyzed with the MicroResp technique5 NH4+, N03- and dissolved organic nitrogen (DON) were estimated by colorimetry from K2SO4 0.5 M extracts in the incubated and initial (air-dried) soil samples2. The potential net N trasnformation rates (depolymerization, ammonification and nitrification; [NTRs]) were calculated for each nutrient treatment3. C NUMERICAL AND STATISTICAL ANALYSES D The Shannon-Weaver (S-W) Diversity Index (H') was calculated by using the CO2 responses to the different C sources. Pi is the % of response of a each C substrate in regard to the total6. Figure 1. Study site. A: Localization of our study site at the Iberian peninsula map; B: semi-arid grassland (Stipa tenacissima L); C: BS microsite (Dominate by Diploschistes diacapsis; ratio C:N: 11.24; pH: 7.2); D: BSC microsite (Ratio C:N: 10.11; pH: 7.4). We calculated the increment in the relative dominance of N-forms (NH4+, N03- and DON), total available N, potential net N transformation rates and SW-diversity index in regard to control. The effects of incubation period, microsite and nutrient treatments on the increment of all these variables in regard to control were tested by using PERMANOVAs7. DISCUSSION In general, when C and P was added, BSC showed a higher increase in DON, depolymerization and the S-W diversity index than bare soil microsite (Fig 1-3). N treatment decrease the microbial functional diversity in both microsites (p<0.01). Complex processes as depolymerization may require a larger and diverse group of heterotrophic microorganisms. Besides, P may be an essential nutrient in BSC communities where N fixation. N addition derived from human activities may have an important impact on the N dynamics and microbial functional diversity8. Changes in the labile C:N ratio more than N availability modulate the N-forms and NTRs in both microsites (Fig 1 and 3). Thus, in the 3-week period of incubation, NO3- and nitrification dominate when N treatments (N and N+P), NH4+ and amonification in the C+N+P treatments and DON and depolymerization when C treatments (C and C+P; p<0.01)9-10. CONCLUDING REMARKS The increase in depolymerization, DON and microbial functional diversity in the BSC microsite with regard to bare soil, when C or P were added, suggest that BSC may confer resistance to this variables to changes in nutrient ratios derived from human activities. Changes in the ratios of labile C:N more than N availability seems to modulate the N dominance form and N transformation processes. Figure 1. Increment in the relative dominance of N-forms (NH4+, NO3and DON) under the different nutrient treatments along the periods of incubation, in the BSC and BS microsites. Means ± SE (n = 5). Figure 2. Increment in the S-W diversity index for the different nutrient treatments along the periods of incubation, in the BSC and BS microsites Means ± SE (n = 5). Figure 3. Increment in the NTRs for the different nutrient treatments, in the BSC and BS microsites. Means ± SE (n = 5). REFERENCES: 1. 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