Carbon allocation under light and nitrogen resource gradients in two model marine phytoplankton1

Marine phytoplankton have conserved elemental stoichiometry, but there can be significant deviations from this Redfield ratio. Moreover, phytoplankton allocate reduced carbon (C) to different biochemical pools based on nutritional status and light availability, adding complexity to this relationship. This allocation influences physiology, ecology, and biogeochemistry. Here, we present results on the physiological and biochemical properties of two evolutionarily distinct model marine phytoplankton, a diatom (cf. Staurosira sp. Ehrenberg) and a chlorophyte (Chlorella sp. M. Beijerinck) grown under light and nitrogen resource gradients to characterize how carbon is allocated under different energy and substrate conditions. We found that nitrogen (N)‐replete growth rate increased monotonically with light until it reached a threshold intensity (~200 μmol photons · m^?2 · s^?1). For Chlorella sp., the nitrogen quota (pg · μm^?3) was greatest below this threshold, beyond which it was reduced by the effect of N‐stress, while for Staurosira sp. there was no trend. Both species maintained constant maximum quantum yield of photosynthesis (mol C · mol photons^?1) over the range of light and N‐gradients studied (although each species used different photophysiological strategies). In both species, C:chl a (g · g^?1) increased as a function of light and N‐stress, while C:N (mol · mol^?1) and relative neutral lipid:C (rel. lipid · g^?1) were most strongly influenced by N‐stress above the threshold light intensity. These results demonstrated that the interaction of substrate (N‐availability) and energy gradients influenced C‐allocation, and that general patterns of biochemical responses may be conserved among phytoplankton; they provided a framework for predicting phytoplankton biochemical composition in ecological, biogeochemical, or biotechnological applications.     

Canopy transpiration of Jeffrey pine in mesic and xeric microsites: O<Subscript>3</Subscript> uptake and injury response

Canopy transpiration of mature Jeffrey pine was compared in "mesic" and "xeric" microsites differing in topographical position, bole growth, and the level of drought stress experienced. Diurnal and seasonal course of canopy transpiration was monitored with thermal dissipation probes in 1999 and 2000. Mid-canopy measures of diurnal foliar stomatal conductance (gs) were taken in June and August in 1999. In early summer, there was little difference between trees in either microsite with regard to gs (55 mmol H2O m⁻²s⁻¹), canopy transpiration (4.0 l h⁻¹), and total duration of active transpiration (12 h >0.03 l h⁻¹). In late summer, xeric trees had a lower daily maximum gs (by 30%), a greater reduction in whole canopy transpiration relative to the seasonal maximum (66 vs 79%), and stomata were open 2 h less per day than in mesic trees. Based on leaf-level gas exchange measurements, trees in mesic sites had an estimated 46% decrease in O3 uptake from June to August. Xeric trees had an estimated 72% decrease over the same time period. A multivariate analysis of morphological and tissue chemistry attributes in mid-canopy elucidated differences in mesic and xeric tree response. Mesic trees exhibited more O3 injury than xeric trees based on reduced foliar nitrogen content and needle retention in mid-canopy.     

Bacillus naphthovorans sp. nov. from oil-contaminated tropical marine sediments and its role in naphthalene biodegradation

. A Bacillus sp., designated as strain MN-003, was isolated as the dominant cultivatable naphthalene-degrading organism from oil-contaminated tropical marine sediments. Strain MN-003 is strictly aerobic, rod-shaped, Gram-positive, catalase positive, oxidase negative, and forms endospores. Strain MN-003 grew at salinities ranging from 0.28 to 7.00% and temperatures ranging from 15 to 41°C. Phylogenetic analyses reveal that strain MN-003 is most similar to Bacillus sp. VAN14, with a 16S rRNA sequence identity of 97.9%. Based on taxonomic and 16S rRNA data, strain MN-003 was named Bacillus naphthovorans sp. nov. When grown with naphthalene as sole carbon source, strain MN-003 had a maximal specific growth rate (µmax) of 0.32ǂ.03 h^–1, and a half-saturation constant (Ks) of 22.3dž.2 µM. A batch study of the tropical marine sediments enriched with naphthalene showed that cells of the Bacillus genus grew to become dominant members of the microbial community. The bacilli comprised 39.5Lj.5% of the microbial fraction after 20 days of enrichment.     

Phytoplankton dynamics in the Congo River

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Plant community structure determines primary productivity in shallow,eutrophic lakes

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Soil carbon and belowground carbon balance of a short‐rotation coppice: assessments from three different approaches

Uncertainty in soil carbon (C) fluxes across different land‐use transitions is an issue that needs to be addressed for the further deployment of perennial bioenergy crops. A large‐scale short‐rotation coppice (SRC) site with poplar (Populus) and willow (Salix) was established to examine the land‐use transitions of arable and pasture to bioenergy. Soil C pools, output fluxes of soil CO₂, CH₄, dissolved organic carbon (DOC) and volatile organic compounds, as well as input fluxes from litter fall and from roots, were measured over a 4‐year period, along with environmental parameters. Three approaches were used to estimate changes in the soil C. The largest C pool in the soil was the soil organic carbon (SOC) pool and increased after four years of SRC from 10.9 to 13.9 kg C m^?2. The belowground woody biomass (coarse roots) represented the second largest C pool, followed by the fine roots (Fr). The annual leaf fall represented the largest C input to the soil, followed by weeds and Fr. After the first harvest, we observed a very large C input into the soil from high Fr mortality. The weed inputs decreased as trees grew older and bigger. Soil respiration averaged 568.9 g C m^?2 yr^?1. Leaching of DOC increased over the three years from 7.9 to 14.5 g C m^?2. The pool‐based approach indicated an increase of 3360 g C m^?2 in the SOC pool over the 4‐year period, which was high when compared with the ?27 g C m^?2 estimated by the flux‐based approach and the ?956 g C m^?2 of the combined eddy‐covariance + biometric approach. High uncertainties were associated to the pool‐based approach. Our results suggest using the C flux approach for the assessment of the short‐/medium‐term SOC balance at our site, while SOC pool changes can only be used for long‐term C balance assessments.     

Invasive submerged freshwater macrophytes are more plastic in their response to light intensity than to the availability of free CO2 in air‐equilibrated water

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Carbon burial by shallow lakes on the Yangtze floodplain and its relevance to regional carbon sequestration

Floodplain lakes may play an important role in the cycling of organic matter at the landscape scale. For those lakes on the middle and lower reaches of the Yangtze (MLY) floodplain which are subjected to intense anthropogenic disturbance, carbon burial rates should, theoretically, be substantial due to the high nutrient input, increased primary production and high sediment accumulation rates. There are more than 600 lakes >1 km² on the Yangtze floodplain including 18 lakes >100 km² and most are shallow and eutrophic. ²¹⁰Pb‐dated cores were combined with total organic carbon (TOC) analyses to determine annual C accumulation rates (C AR; g C m^?2 yr^?1) and the total C stock (since ~1850). The sediment TOC content is relatively low with an average <2% in most lakes. C AR ranged from ~5 to 373 g C m^?2 yr^?1, resulting in C standing stocks of 0.60–15.3 kg C m^?2 (mean: ~5 kg C m^?2) since ~1850. A multicore study of Chaohu lake (770 km²) indicated that spatial variability of C burial was not a significant problem for regional upscaling. The possible effect of changes in lake size and catchment land use on C burial was examined at Taibai lake and indicated that lake shrinkage and declining arable agriculture had limited effects on C AR. The organic C standing stock in individual lakes is, however, significantly dependent on lake size, allowing a simple linear scaling for all the MLY lakes. Total regional C sequestration was ~80 Tg C since ~1850, equivalent to ~11% of C sequestration by soils, but in ~3% of the land area. Shallow lakes from MLY are a substantial regional C sink, although strong mineralization occurs due to their shallow nature and their role as C sinks is threatened due to lake drainage.     

A difference in optomotor behaviour of two Antarctic nototheniid fishes is correlated with the presence of a choroid<Emphasis Type="Italic"> rete mirabile</Emphasis> and Root effect

The hypothesis that fish vision is influenced by the presence of a choroid rete mirabile (an oxygen-concentrating apparatus in the eye) and the Root effect was tested using the optomotor response in two nototheniid species from Antarctica. Pagothenia borchgrevinki, an active cryopelagic zooplanktivore, does not exhibit a major Root effect and the rete is absent. In contrast, the sluggish, benthic nototheniid, Trematomus bernacchii, possesses both a rete and a significant Root effect. Whole-eye ocular PO2 was higher in T. bernacchii (18.6 kPa) than in P. borchgrevinki (18.1 kPa) and the optomotor response of T. bernacchii was positively influenced by subtended angle on a moving background whereas P. borchgrevinki did not respond to any subtended angle (0–600 min of arc). The optomotor response of T. bernacchii may therefore have been facilitated by elevated ocular PO2 due to the presence of the choroid rete and the Root effect.     

The maximum quantum yield of phylopiankton photosynthesis in situ

Light-limited photosynthetic carbon incorportion is expectedto be directly proportional to the scalar quantum irradiance.The proportionality constant is , where _mis the maximum quantum yield (mol C Einstein^–1 absorbed)and $$\stackrel{\&macr;}{{\hbox{ k }}_{\hbox{ c }}}$$ isthe mean spectral absorption coefficient (m² mg^–1 chla). Recent efforts to evaluate of in situphytoplankton photosynthesis are variously flawed. Lack of evidenceof proportionality and lack of correction of cosine to scalarirradiance are common deficiencies. Most data, as we interpretthem, indicate values in the range 0.0003 – 0.0006 mol C m² Einstein1 abs mg1 chl a. New determinationsin lrondequoit Bay, New York, lie in this range. Most estimatesof at depth have been about 0.010 m² mg^–1chl a. Similar values are being obtained for total particulatesfrom lrondequoit Bay; whether detritus contributes significantlyis not yet known. Published data, in our view, all point tovalues of m in situ in the range 0.03–0.07 mol C Einstein^–1abs. Published values >0.10 are almost certainly due to imprecisionor systematic error. ^*This paper is the result of a study made at the Group for AquaticPrimary Productivity (GAP) First International Workshop heldat the Limnological Institute, University of Konstanz, in April1982.     

Using CO2 to enhance carbon capture and biomass applications of freshwater macroalgae

A major limiting factor in the development of algae as a feedstock for the bioenergy industry is the consistent production and supply of biomass. This study is the first to access the suitability of the freshwater macroalgal genus Oedogonium to supply biomass for bioenergy applications. Specifically, we quantified the effect of CO₂ supplementation on the rate of biomass production, carbon capture, and feedstock quality of Oedogonium when cultured in large‐scale outdoor tanks. Oedogonium cultures maintained at a pH of 7.5 through the addition of CO₂ resulted in biomass productivities of 8.33 (±0.51) g DW m^?2 day^?1, which was 2.5 times higher than controls which had an average productivity of 3.37 (±0.75) g DW m^?2 day^?1. Under these productivities, Oedogonium had a carbon content of 41–45% and a higher heating value of 18.5 MJ kg^?1, making it an ideal biomass energy feedstock. The rate of carbon fixation was 1380 g C m^?2 yr^?1 and 1073.1 g C m^?2 yr^?1 for cultures maintained at a pH of 7.5 and 8.5, and 481 g C m^?2 yr^?1 for cultures not supplemented with CO₂. This study highlights the potential of integrating the large‐scale culture of freshwater macroalgae with existing carbon waste streams, for example coal‐fired power stations, both as a tool for carbon sequestration and as an enhanced and sustainable source of bioenergy.     

Production rate estimation of mycosporine‐like amino acids in two Arctic melt ponds by stable isotope probing with NAH13CO3

The net carbon uptake rate and net production rate of mycosporine‐like amino acids (MAAs) were measured in phytoplankton from 2 different melt ponds (MPs; closed and open type pond) in the western Arctic Ocean using a ¹³C stable isotope tracer technique. The Research Vessel Araon visited ice‐covered western‐central basins situated at 82°N and 173°E in the summer of 2012, when Arctic sea ice declined to a record minimum. The average net carbon uptake rate of the phytoplankton in polycarbonate (PC) bottles in the closed MP was 3.24 mg C · m^?3 · h^?1 (SD = ±1.12 mg C · m^?3 · h^?1), while that in the open MP was 1.3 mg C · m^?3 · h^?1 (SD = ±0.05 mg C · m^?3 · h^?1). The net production rate of total MAAs in incubated PC bottles was highest (1.44 (SD = ±0.24) ng C · L^?1 · h^?1) in the open MP and lowest (0.05 (SD = ±0.003) ng C · L^?1 · h^?1) in the closed MP. The net production rate of shinorine and palythine in incubated PC bottles at the open MP presented significantly high values 0.76 (SD = ±0.12) ng C · L^?1 · h^?1and 0.53 (SD = ±0.06) ng C · L^?1 · h^?1. Our results showed that high net production rate of MAAs in the open MP was enhanced by a combination of osmotic and UVR stress and that in situ net production rates of individual MAA can be determined using ¹³C tracer in MPs in Arctic sea ice.     

Carbon dioxide exchange dynamics over a mature switchgrass stand

Switchgrass (Panicum virgatum L.) has gained importance as feedstock for bioenergy over the last decades due to its high productivity for up to 20 years, low input requirements, and potential for carbon sequestration. However, data on the dynamics of CO₂ exchange of mature switchgrass stands (>5 years) are limited. The objective of this study was to determine net ecosystem exchange (NEE), ecosystem respiration (Re), and gross primary production (GPP) for a commercially managed switchgrass field in its sixth (2012) and seventh (2013) year in southern Ontario, Canada, using the eddy covariance method. Average NEE flux over two growing seasons (emergence to harvest) was ?10.4 μmol m^?2 s^?1 and reached a maximum uptake of ?42.4 μmol m^?2 s^?1. Total annual NEE was ?380 ± 25 and ?430 ± 30 g C m^?2 in 2012 and 2013, respectively. GPP reached ?1354 ± 23 g C m^?2 in 2012 and ?1430 ± 50g C m^?2 in 2013. Annual Re in 2012 was 974 ± 20 g C m^?2 and 1000 ± 35 g C m^?2 in 2013. GPP during the dry year of 2012 was significantly lower than that during the normal year of 2013, but yield was significantly higher in 2012 with 1090 g  m^?2, compared to 790 g m^?2 in 2013. If considering the carbon removed at harvest, the net ecosystem carbon balance came to 106 ± 45 g C  m^?2 in 2012, indicating a source of carbon, and to ?59 ± 45 g C m^?2 in 2013, indicating a sink of carbon. Our results confirm that switchgrass can switch between being a sink and a source of carbon on an annual basis. More studies are needed which investigate this interannual variability of the carbon budget of mature switchgrass stands.     

PHOTOACCLIMATION OF PHOTOSYNTHESIS IRRADIANCE RESPONSE CURVES AND PHOTOSYNTHETIC PIGMENTS IN MICROALGAE AND CYANOBACTERIA1

The photosynthesis‐irradiance response (PE) curve, in which mass‐specific photosynthetic rates are plotted versus irradiance, is commonly used to characterize photoacclimation. The interpretation of PE curves depends critically on the currency in which mass is expressed. Normalizing the light‐limited rate to chl a yields the chl a‐specific initial slope (α^chl). This is proportional to the light absorption coefficient (a^chl), the proportionality factor being the photon efficiency of photosynthesis (φ_m). Thus, α^chl is the product of a^chl and φ_m. In microalgae α^chl typically shows little (<20%) phenotypic variability because declines of φ_m under conditions of high‐light stress are accompanied by increases of a^chl. The variation of α^chl among species is dominated by changes in a^chl due to differences in pigment complement and pigment packaging. In contrast to the microalgae, α^chl declines as irradiance increases in the cyanobacteria where phycobiliproteins dominate light absorption because of plasticity in the phycobiliprotein:chl a ratio. By definition, light‐saturated photosynthesis (P_m) is limited by a factor other than the rate of light absorption. Normalizing P_m to organic carbon concentration to obtain P_m^C allows a direct comparison with growth rates. Within species, P_m^C is independent of growth irradiance. Among species, P_m^C covaries with the resource‐saturated growth rate. The chl a:C ratio is a key physiological variable because the appropriate currencies for normalizing light‐limited and light‐saturated photosynthetic rates are, respectively, chl a and carbon. Typically, chl a:C is reduced to about 40% of its maximum value at an irradiance that supports 50% of the species‐specific maximum growth rate and light‐harvesting accessory pigments show similar or greater declines. In the steady state, this down‐regulation of pigment content prevents microalgae and cyanobacteria from maximizing photosynthetic rates throughout the light‐limited region for growth. The reason for down‐regulation of light harvesting, and therefore loss of potential photosynthetic gain at moderately limiting irradiances, is unknown. However, it is clear that maximizing the rate of photosynthetic carbon assimilation is not the only criterion governing photoacclimation.     

Moderate weather extremes alter phytoplankton diversity—A microcosm study

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Phytoplankton and sea ice algal biomass and physiology during the transition between winter and spring (McMurdo Sound, Antarctica)

The phytoplankton and sea ice algal communities at the end of winter in McMurdo Sound were dominated by Fragilariopsis sublineata, with Thalassiosira antarctica, Melosira adele, Pinnularia quadreata, Entomoneis kjellmannii and heterotrophic dinoflagellates also present. Sea ice algal biomass at the end of winter was very low, only 0.050 ± 0.019 mg chla m⁻² in 2007 and 0.234 ± 0.036 mg chla m⁻² in 2008, but this increased to 0.377 ± 0.078 mg chla m⁻² by early October in 2007 and to 1.07 ± 0.192 by late September in 2008. Under ice phytoplankton biomass remained consistently below 0.1 μg chla l⁻¹ throughout the measuring period in both years. The photosynthetic parameters Fv/Fm, rETRmax and α document microalgal communities that are mostly healthy and well adapted to their low light under ice environment. Our results also suggest that species such as Fragilariopsis sublineata are well adapted to deal with low winter light levels but are unlikely to survive an increase in irradiance, whereas other taxa, such as Thalassiosira antarctica, will do better in a higher light environment.     

Planktonic primary production in the German Wadden Sea

By combining weekly data of irradiance, attenuation and chlorophylla concentrations with photosynthesis (P) versus light intensity(E) curve characteristics, the annual cycle of planktonic primaryproduction in the estuarine part of the Northfrisian WaddenSea was computed for a 2 year period. Daily water column particulategross production ranged from 5 to 2200 mg C m^–2 day^–1and showed a seasonal pattern similar to chlorophyll a. Budgetcalculation yielded annual gross particulate primary productionsof 124 and 176 g C m^–2 year^–1 in 1995 and 1996,respectively. Annual amounts of phytoplankton respiration, calculatedaccording to a two-compartment model of Langdon [in Li,W.K.W.and Maestrini,S.Y. (eds), Measurement of Primary Productionfrom the Molecular to the Global Scale. International Councilfor the Exploration of the Sea, Copenhagen, 1993, pp. 20–36],and dissolved production in 1996, were both in the range of24–39 g C m^–2 year^–1. Annual total net productionwas thus very similar to particulate gross production (127 and177 g C m^–2 year^–1 in 1995 and 1996, respectively).Phytoplankton growth was low or even negative in winter. Inspring and summer, production/biomass (Pr/B) ratios varied from0.2 up to 1.7. Phytoplankton growth during the growth seasonalways surpassed average flushing time in the area, thus underliningthe potential of local phytoplankton bloom development in thispart of the Wadden Sea. The chlorophyll-specific maximum photosyntheticrate (P^B_max) ranged from 0.8 to 9.9 mg C mg^–1 Chl h^–1and was strongly correlated with water temperature (r² = 0.67).By contrast, there was no clear seasonal cycle in ^B, which rangedfrom 0.007 to 0.039 mg C mg^–1 Chl h^–1 (µmolphotons m^–2 s^–1)^–1. Its variability was muchless than P^B_max and independent of temperature. The magnitudeand part of the variability of P^B_max and ^B are presumably causedby changes in species composition, as evidenced from the rangeof these parameters found among 10 predominant diatom speciesisolated from the Wadden Sea. The ratio of average light conditionsin the water column (E_av) to the light saturation parameterE_k indicates that primary production in the Wadden Sea regionunder study is predominantly controlled by light limitationand that nutrient limitation was likely to occur for a few hoursper day only during 5 (dissolved inorganic nitrogen) to 10 (PO₄,Si) weeks in the 2 year period investigated.     

The optical properties of a turbid reservoir and its phytoplankton in relation to photosynthesis and growth (Mount Bold Reservoir, South Australia)

In situ light measurements were used to obtain information oninherent and apparent optical properties. The average verticalattenuation coefficient K_d(ave) varied from 1.1 to 4.6 In unitsm^–1 During three periods the variation in K_d(ave) correlatedwith changes in chlorophyll a concentration and specific attenuationcoefficients K_s, of 0.013, 0.014 and 0.022 m² mg Chl a^–1were calculated. Chlorophyll-specific diffuse absorption coefficients(A,) for these periods were 0.012. 0.013 and 0.017 m² mg Chla^–1 and only varied significantly from estimates of K_sin the period when scattering was intense. Absorption coefficientsa(z^mid) and scattering coefficients b(z^mid) calculated for themid-point of the euphotic zone ranged between 0.45 and 2.9 mand 3.5–52.0 m respectively. Chlorophyll-specific absorptioncoefficients K_a, of 0.005, 0.006 and 0.007 m² mg Chl a^–1and scattering coefficients K_b of 0.05. 0.09 and 0.191 m² mgChl a^–1 were measured during the three periods. The highK_b value occurred when gas-vacuolate cyanobactena were dominant.Algal photosynthesis and light absorption were related throughthe maximum quantum yield _m which varied between 0.019 and 0.11mol C Einstein^–1 while average quantum yields _a, variedbetween 0.006 and 0.024 with a mean of 0.013 mol C Einstein^–1A comparison of changes in the mean irradiance of the mixedzone and chlorophyll concentration indicated that growth waslight limited below 0.04–0.05 Einsteins absorbed mg Chla^–1 day^–1.     

低温弱光胁迫及恢复对切花菊光合作用和叶绿素荧光参数的影响

以切花菊品种‘神马’为试材,在偏低温弱光(16℃/12℃,PFD100μmol.m-2.s-1)和临界低温弱光(12℃/8℃,PFD60μmol.m-2.s-1)下分别胁迫11d,然后转入正常条件(22℃/18℃,PFD450μmol.m-2.s-1)恢复11d,研究不同低温弱光强度及恢复对菊花光合作用和叶绿素荧光参数的影响.结果表明:低温弱光导致菊花叶片的净光合速率(Pn)和气孔限制值(Ls)下降,而胞间CO2浓度(Ci)上升.偏低温弱光胁迫下菊花叶片暗适应下最大光化学效率(Fv/Fm)和初始荧光(Fo)无明显变化,但光适应下最大光化学效率(Fv′/Fm′)在处理前期略有下降,后期则有所回升;而临界低温弱光处理的Fo明显升高,Fv/Fm和Fv′/Fm′显著降低.PSⅡ光合电子传递量子效率(ΦPSⅡ)、光化学猝灭系数(qP)和表观光合电子传递速率(ETR)均随着低温弱光胁迫程度的增加和时间的延长而降低;偏低温弱光处理植株在解除胁迫后能迅速恢复到对照水平,而临界低温弱光处理植株回升速度较慢;同时,低温弱光胁迫下吸收光强用于分配光化学反应部分(Prate)的比例减少,而天线热耗散(Drate)和反应中心的能量耗散(Ex)比例上升,但天线热耗散为过剩光能的主要分配途径.     

Relationship Between Root Biomass and Soil Organic Matter Pools in the Shortgrass Steppe of Eastern Colorado

We examined the distribution of soil organic carbon (SOC) fractions and roots with depth to improve our understanding of belowground carbon dynamics in the shortgrass steppe of northern Colorado. Weaver and others (1935) found that the surface 15 cm of soil contained over 70% of the total roots found in a tallgrass prairie soil profile, while only accounting for 40% of the profile soil organic matter. We asked whether the relationship between roots and SOC that Weaver and others (1935) found in the tallgrass prairie was also found in the shortgrass steppe. Weaver and others (1935) suggested that the dissimilarity between belowground biomass and SOC with depth is the result of variability in decomposition rates. In an effort to determine whether patterns of SOC are the result of short-term plant input patterns or decomposition, we measured the ¹⁴C content of potentially mineralizable C and particulate organic matter (POM) C ten years after pulse labeling shortgrass steppe vegetation. We also estimated the mass specific decomposition rate constant (kPOM) for POM C through a shortgrass steppe soil profile. We found that the distribution of roots and SOM in the shortgrass steppe were similar to those observed in tallgrass prairie (Weaver and others 1935), with a higher proportion of total root biomass in the surface soils than total soil organic matter. Fifty-seven percent of root biomass was found in the surface 15-cm, while this same soil layer contained 23 percent of profile soil organic C. We measured the highest accumulation of ¹⁴C at the soil surface (12.0 ng ¹⁴C·m^-2·cm^-1 depth), with the least accumulation from 75-100 cm (0.724 ng ¹⁴C·m^-2·cm^-1 depth). The highest values of potentially mineralizable C were at the soil surface, with no significant differences in total mineralizable C among the 10-100 cm soil depths. The contribution of POM C to total C reached a profile minimum at the 15-20 cm depth increment, with profile maxima in the surface 5 cm and from 75-100 cm. We estimated that the proportion of particulate organic matter lost annually (kPOM) reached a profile maximum of 0.097 yr^-1 within the 10-15 cm depth increment. The 75-100 cm depth increment had the lowest kPOM value at 0.058 yr^-1. Thus, within the same physical fraction of SOC, decomposition rates vary with depth by nearly twofold. This pattern of high decomposition rates from 10-15 cm with lower decomposition rates at the soil surface and deeper in the soil profile may be the result of higher water availability in sub-surface soils in the shortgrass steppe.