Abstract

Abstract. Biological soil crusts (biocrusts) are a common element of the Queensland (Australia) dry savannah ecosystem and are composed of cyanobacteria, algae, lichens, bryophytes, fungi and heterotrophic bacteria. Here we report how the CO2 gas exchange of the cyanobacteria-dominated biocrust type from Boodjamulla National Park in the north Queensland Gulf Savannah responds to the pronounced climatic seasonality and on their quality as a carbon sink using a semi-automatic cuvette system. The dominant cyanobacteria are the filamentous species Symplocastrum purpurascens together with Scytonema sp. Metabolic activity was recorded between 1 July 2010 and 30 June 2011, during which CO2 exchange was only evident from November 2010 until mid-April 2011, representative of 23.6 % of the 1-year recording period. In November at the onset of the wet season, the first month (November) and the last month (April) of activity had pronounced respiratory loss of CO2. The metabolic active period accounted for 25 % of the wet season and of that period 48.6 % was net photosynthesis (NP) and 51.4 % dark respiration (DR). During the time of NP, net photosynthetic uptake of CO2 during daylight hours was reduced by 32.6 % due to water supersaturation. In total, the biocrust fixed 229.09 mmol CO2 m−2 yr−1, corresponding to an annual carbon gain of 2.75 g m−2 yr−1. Due to malfunction of the automatic cuvette system, data from September and October 2010 together with some days in November and December 2010 could not be analysed for NP and DR. Based on climatic and gas exchange data from November 2010, an estimated loss of 88 mmol CO2 m−2 was found for the 2 months, resulting in corrected annual rates of 143.1 mmol CO2 m−2 yr−1, equivalent to a carbon gain of 1.7 g m−2 yr−1. The bulk of the net photosynthetic activity occurred above a relative humidity of 42 %, indicating a suitable climatic combination of temperature, water availability and light intensity well above 200 µmol photons m−2 s−1 photosynthetic active radiation. The Boodjamulla biocrust exhibited high seasonal variability in CO2 gas exchange pattern, clearly divided into metabolically inactive winter months and active summer months. The metabolic active period commences with a period (of up to 3 months) of carbon loss, likely due to reestablishment of the crust structure and restoration of NP prior to about a 4-month period of net carbon gain. In the Gulf Savannah biocrust system, seasonality over the year investigated showed that only a minority of the year is actually suitable for biocrust growth and thus has a small window for potential contribution to soil organic matter.

Highlights

  • Biological soil crusts are a consortium of heterotrophic bacteria, cyanobacteria, algae, fungi, lichens and bryophytes in different proportions with photoautotrophic organisms dominating their biomass

  • Our results showed that the Boodjamulla biocrust exhibited a positive net C uptake after the 1-year field monitoring period. This result is in line with the findings of several other studies but differs from all of them in the fact that our study focused on an environment with hot wet-season hydration, whereas all other studies were conducted in environments with cool season hydration

  • What are the reasons for negative C balances of the biocrusts during the first active months after start of the rainy season? We suggest that in contrast to eukaryotic poikilohydric photoautotrophs such as liverworts, mosses or lichens, which resuscitate all thallus compartments after hydration, prokaryotic cyanobacteria show considerable dieback rates during longer dry periods or drought events

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Summary

Introduction

Biological soil crusts (named “biocrusts” throughout the text) are a consortium of heterotrophic bacteria, cyanobacteria, algae, fungi, lichens and bryophytes in different proportions with photoautotrophic organisms dominating their biomass. They cover dryland soil surfaces and can compose up to 70 % of a dryland ecosystem’s living cover (Belnap, 1995; Belnap et al, 2016), and occur in other climatic regions where competition with vascular plants is low (Büdel, 2001; Büdel et al, 2014). Lalonde and Konhauser (2015) point to the importance of oxygenic photosynthesis of early biocrusts providing sufficient equivalents for oxidative-weathering reactions in benthic and soil environments. Process-based models as used by Porada et al (2013, 2014) still rely on a few available data sets covering a small number of biocrust types, organisms, geographical regions and climatic conditions (see summary in Sancho et al, 2016)

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