PL EN
ORIGINAL PAPER
State of soil enzymatic activity in relationship to some chemical properties of Brunic Arenosols
 
More details
Hide details
1
Wydział Leśny, Katedra Ekologii i Hodowli Lasu, Uniwersytet Rolniczy im. Hugona Kołłątaja w Krakowie, Polska
 
 
Submission date: 2021-02-23
 
 
Final revision date: 2021-04-14
 
 
Acceptance date: 2021-07-30
 
 
Online publication date: 2021-12-31
 
 
Publication date: 2021-12-31
 
 
Corresponding author
Wojciech Piaszczyk   

Wydział Leśny, Katedra Ekologii i Hodowli Lasu, Uniwersytet Rolniczy im. Hugona Kołłątaja w Krakowie, Polska
 
 
Soil Sci. Ann., 2021, 72(4)140641
 
KEYWORDS
ABSTRACT
Brunic Arenosols are one of the most common soil types in lowland forests. The aim of this study was to determine the enzymatic activity of trophically diverse forest Brunic Arenosols. In this study, an attempt was made to determine the relationship between enzymatic activity and some chemical properties of Brunic Arenosols. It has been presented how the activity of dehydrogenases, urease and protease changes deep into the profile of Brunic Arenosols. Sample plots were located in central Poland, in the Przedbórz forest district. 23 sample plots have been selected for the research. The research concerned Albic Brunic Arenosols (9 plots), Haplic Brunic Arenosols (7 plots) and Cambic Brunic Arenosols (7 plots). At each sample plot a detailed description of soil profile has been carried out, samples have been taken from each genetic horizon in order to mark of soil properties and enzyme activity. The analyses carried out confirmed the relationship of enzymatic activity with the content of C, N, pH and the texture in the studied soils. Regardless of the type of enzyme, a decrease in activity has been observed in the depth of the profile which is related to the availability of carbon substrates necessary for enzymatic reactions. Dehydrogenases activity reflects the trophic conditions of Brunic Arenosols better than other tested enzymes. The highest dehydrogenases activity was recorded in Cambic Brunic Arenosols. For protease and urease activities, no clear differences were recorded between Brunic Arenosols subtypes. Extracellular enzyme activities were most strongly associated with organic horizons regardless of Brunic Arenosols subtype.
 
REFERENCES (36)
1.
Alef, K., Nannipieri, P., 1995. Enzyme activities. [In:] Methods in applied Soil Microbiology and Biochemistry (Alef K., Nannipieri P., Editors). Academic Press, London, New York, San Francisco, 311-373.
 
2.
Allison, S., Wallenstein, M., Bradford, M., 2010. Soil-carbon response to warming dependent on microbial physiology. Nature Geoscience 3, 336-340. https://doi.org/10.1038/ngeo84....
 
3.
Bach, E.M., Hofmockel, K.S., 2014. Soil aggregate isolation metod affects measures of intra-aggregate extracellular enzyme activity. Soil Biology and Biochemistry 69, 54-62.
 
4.
Baldrian, P., 2014. Distribution of extracellular enzymes in soils: spatial heterogeneity and determining factors AT various scales. Soil Science Society of America Journal 78, 11-18. https://doi.org/10.2136/sssaj2....
 
5.
Baran, S., Bielińska, J.E., Oleszczuk, P., 2004. Enzymatic activity in an airfield soil polluted with polycyclic aromatic hydrocarbons. Geoderma 118, 221-232. https://doi.org/10.1016/S0016-....
 
6.
Błońska, E., Lasota, J., Gruba, P., 2016. Effect of temperate forest tree species on soil dehydrogenase and urease activities in relation to other properties of soil derived from loess and glaciofluvial sand. Ecological Research 31(5), 655-664.
 
7.
Błońska, E., Bednarz, B., Kacprzyk, M., Piaszczyk, W., Lasota, J., 2020a. Effect of Scots pine forest management on soil properties and carabid beetle occurrence under post-fire environmental conditions - a case study from Central Europe. Forest Ecosystems 7, 28. https://doi.org/10.1186/s40663....
 
8.
Błońska, E., Lasota, J., Rocha Vasconcelos da Silva, G., Vanguelova, E., Ashwood, F., Tibbett, M., Watts, K., Lukac, M., 2020b. Soil organic matter stabilization and carbon-cycling enzyme activity are affected by land management. Annals of Forest Research 63, 71-86.
 
9.
Błońska, E., Piaszczyk, W., Staszel, K., Lasota, J., 2021. Enzymatic activity of soils and soil organic matter stabilization as an effect of components released from the decomposition of litter. Applied Soil Ecology 157, 103723. https://doi.org/10.1016/j.apso....
 
10.
Burns, R.G., Dick, R.P., 2002. Enzymes in the environment: activity, ecology and applications. Mercel Dekker, New York, 1-640.
 
11.
Cusack, D.F., Silver, W.L., Torn, M.S., Burton, S.D., Firestone, M.K., 2011. Changes in microbial community characteristics and soil organic matter with nitrogen additions in two tropical forests. Ecology 92, 621-632. https://doi.org/10.1890/10-045....
 
12.
Everrit, B., 1980. Cluster analysis. Reviews of current research. Social Science Research Council, Halstead Press, New York, pp. 11.
 
13.
Frankenberger, W.T., Johanson, J.B., 1982. Effect of pH on enzyme stability in soil. Soil Biology and Biochemistry 14, 433-437.
 
14.
Friedlová, M., 2010. The influence of heavy metals on soil biological and chemical properties. Soil Water Research 5, 21–27. https://doi.org/10.17221/11/20....
 
15.
Gianfreda, L., Rao, A.M., Piotrowska, A., Palumbo, G., Colombo, C., 2005. Soil enzyme activities as affected by anthropogenic alterations: intensive agricultural practices and organic pollution. Science of the Total Environment 341, 265-79.
 
16.
Haziev, F.H., 1976. Fermentativnaâ aktivnost počv. Izd. Nauka, Moskwa.
 
17.
Hernández, D.L., Hobbie, S.E., 2010. The effects of substrate composition quantity, and diversity on microbial activity. Plant and Soil 335, 397-411. https://doi.org/10.1007/s11104....
 
18.
Kandeler, E., Stemmer, M, Klimanek, E.M., 1999. Response of soil microbial biomass, urease and xylanase within particle size fraction to long-term soil management. Soil Biology and Biochemistry 31, 261–273.
 
19.
Klasyfikacja Gleb Leśnych Polski. 2000. CILP Warszawa.
 
20.
Kotroczó, Z., Veres, Z., Fekete, J., Krakomperger, Z., Tóth, J.A., Lajtha, K., Tóthmérész, B., 2014. Soil enzyme activity in response to long-term organic matter manipulation. Soil Biology and Biochemistry 70: 237-243. https://doi.10.1016/j.soilbio.....
 
21.
Kumar, S., Chaudhuri, S., Maiti S.K., 2013. Soil dehydrogenase enzymes activity in natural and mine soil—a review. Middle East Journal Science Research 13, 898–906. https://doi.10.5829/idosi.mejs....
 
22.
Lasota J, Błońska E., 2013. Forest Site Science in the Polish Lowlands and Highlands; Scientific Papers; University of Agriculture in Krakow, Kraków, Poland.
 
23.
Lasota, J., Błońska, E., 2018. Polycyclic aromatic hydrocarbons content in contaminated forest soils with different humus type. Water Air and Soil Pollution 229, 204. https://doi.org/10.1007/s11270....
 
24.
Ling, N., Sun, Y., Ma, J., Guo, J., Zhu, P., Peng, C., Yu, G., Rau, W., Guo, S., Shen, Q., 2014. Response of the bacterial diversity and soil enzyme activity in particle-size fraction of Mollisol after different fertilization in a long-term experiment. Biology Fertility of Soil 50, 901–911.
 
25.
Lipińska, A., Kucharski, J., Wyszkowska, J., 2013. Urease activity in soil contamined with polycyclic aromatic hydrocarbons. Polish Journal of Environmental Studies 22, 1393-1400.
 
26.
Margesin, R., Zimmerbauer, A., Schinner, F., 2000. Monitoring of bioremediation by soil biological activities. Chemosphere 40, 339-346. https://doi.org/10.1016/S0045-....
 
27.
Sardans, J., Peñuelas, J., Estiarte, M., 2008. Changes in soil enzymes related to C and N cycle and in soil C and N content under prolonged warming and drought in a Mediterranean shrubland. Applied Soil Ecology 39, 223-235. https://doi.org/10.1016/j.apso....
 
28.
Schimel, J.P., Weintraub, M., 2003. The implications of exoenzyme activity on microbial carbon and nitrogen limitation in soil: a theoretical model. Soil Biology and Biochemistry 35, 549-563. https://doi.org/10.1016/S0038-....
 
29.
Sinsabaugh, R.L., Lauber, C.L., Weintraub, M.N., Ahmed, B., Allison, S.D., Crenshaw, C., Contosta, A.R., Causack, D., Frey, S., Gallo, M.E., Gartner, T.B., Hobbie, S.E., Holland, K., Keeler, B.L., Powers, J.S., Stursova, M., Takacs-Vesbach, C., Wallenstein, M.D., Zak, D.R., Zeglin, L.H., 2008. Stoichiometry of soil enzyme activity at global scale. Ecology Letters 11, 1252-1264. https://doi.org/10.1111/j.1461....
 
30.
StatSoft Inc., 2012. STATISTICA (version 13.0). Computer software.
 
31.
Stone, M.M., DeForest, J.L., Plante, A.F., 2014. Changes in extracellular enzyme activity and microbial community structure with soil depth at the Luquillo Critical Zone Observatory. Soil Biology and Biochemistry 75, 237- 247. https://doi.org/ 10.1016/j.soilbio.2014.04.017.
 
32.
Tabatabai, M.A., Bremner, J.M., 1972. Assay of urease activity in soils. Soil Biology and Biochemistry, 4, 479–487.
 
33.
Wang, R., Dorodnikov, M., Yang, S., Zhang, Y., Filley, T.R., Turco, R.F., Zhang, Y., Xu, Z., Li, H., Jiang, Y., 2015. Responses of enzymatic activities within soil aggregates to 9-year nitrogen and water addition in a semi-arid grassland. Soil Biology and Biochemistry 81, 159-167.
 
34.
Wolińska, A., Stępniewska, Z., 2012. Dehydrogenase activity in the soil environment. In: Canuto RA (eds) Dehydrogenases. In-Tech.
 
35.
Quiquampoix, H., Staunton, S., Baron, M.H., Ratkliffe, R.G., 1993. Interpretation of the pH dependence of protein adsorption on clay mineral surfaces and its relevance to the understanding of extracellular enzyme activity in soil. Colloids and Surfaces A: Physicochemical and Engineering Aspects 75, 85-93.
 
36.
Zhan, X., Wu, W., Zhou, L., Liang, J., Jiang, T., 2010. Interactive effect of dissolved organic matter and phenanthrene on soil enzymatic activities. Journal of Environmental Science 22, 607-614. https://doi.org/10.1016/S1001-....
 
eISSN:2300-4975
ISSN:2300-4967
Journals System - logo
Scroll to top