For S elongatus, circadian oscillation

For S. elongatus, circadian oscillation Roxadustat patterns have been demonstrated for almost all genes or at least 30% of all genes, depending on the experimental set-up, conditions and data analysis ( Ito et al., 2009, Liu et al., 1995, Nakahira et al., 2004 and Vijayan

et al., 2009). The consensus view of the clock output pathway is that factors such as SasA, RpaA, LabA as well as CikA with its dual role in input and output regulate downstream gene expression, including kaiBC expression ( Gutu and O’Shea, 2013, Iwasaki et al., 2000, Schmitz et al., 2000, Takai et al., 2006 and Taniguchi et al., 2007). In particular, the histidine kinase SasA (Synechococcus adaptive sensor) constitutes a key component of the output pathway. It interacts physically with KaiC, autophosphorylates and transfers the phosphate to its cognate OmpR-type response regulator RpaA (regulator of phycobilisome-associated; Iwasaki et al., 2000 and Takai et al., 2006). Phosphorylated RpaA

activates kaiBC expression through a so far unknown mechanism because its direct binding has not been shown ( Hanaoka et al., 2012). Activation of kaiBC expression via the KaiC-SasA-RpaA pathway is proposed to occur mainly during the day ( Taniguchi et al., 2010). this website LabA (low-amplitude and bright) and CikA, on the other hand, repress RpaA activity and constitute negative regulators of kaiBC expression ( Gutu and O’Shea, 2013, Taniguchi et al., 2007 and Taniguchi et al., 2010). In a complementary scenario, the circadian clock might regulate gene expression globally by controlling compaction of the chromosome and Pregnenolone DNA supercoiling ( Mori and Johnson, 2001, Smith and Williams, 2006, Vijayan et al., 2009 and Woelfle et al., 2007). Detailed knowledge on how the circadian clock works in the marine lineage of Cyanobacteria is missing due to the lack of effective genetic manipulation systems. Nevertheless, several studies have been published generating the basis of our

present knowledge of circadian and diel regulation in marine species. Some of the first examples for daily oscillations have been reported for nitrogen fixation in marine Cyanobacteria. They very likely orchestrate their metabolic activities with a circadian clock and, in doing so have found different strategies to protect their nitrogenase from damage by photosynthetically produced oxygen. For instance, Cyanothece sp. ATCC 51142 and Crocosphaera watsonii WH 8501 segregate nitrogen fixation and photosynthesis in time ( Pennebaker et al., 2010 and Reddy et al., 1993), and Trichodesmium erythraeum IMS 101 lowers oxygen in the vicinity of nitrogenase in anticipation of nitrogen fixation ( Berman-Frank et al., 2001). Gene expression studies demonstrated circadian rhythmicity for individual genes in T. erythraeum IMS101 and C. watsonii WH 8501 ( Chen et al., 1996, Chen et al.

If the input rate of SiO3-Si is lower than the export rate, SiO3-

If the input rate of SiO3-Si is lower than the export rate, SiO3-Si will eventually be depleted by diatom uptake. It is clear from Figure 4a that the SiO3-Si concentration in the northern part of the cold eddy was so low that it could not markedly indicate the upwelling. The SiO3-Si at the centres of the upwellings in the TSLS and in the west of the PIS was not depleted by diatoms. This confirmed that the upwelling in the TSLS and the upwelling in the west of the PIS were stronger than that in the northern part of the cold eddy, with the one in find more the TSLS being the strongest. With the aid of multivariate statistical analysis and remote sensing techniques, we successfully demonstrated

that silicate is a useful indicator of the formation and distribution of upwelling events in the northern part of the SCS, especially for the analysis and interpretation of complex data from large areas, such as for marine environmental and ecological research (Wang et al. 2006, Chau & Muttil 2007, Suikkanen et al. 2007, Wu & Wang 2007, Wu et al. 2009a,b). Although the complex datasets used here consist of 32 × 14 observations in a large area (18°–23°N, 111°–120°E), the CA clearly distinguished the spatial similarity reflecting different levels of nutrient concentration

(low and high nutrient), and the PCA was successful in picking out silicate as an indicator for studying upwelling. The spatial distribution E7080 in vivo of silicate clearly showed three upwelling regions that can be verified by satellite observations of sea surface temperature. “
“The physiology of all organisms is affected by temperature; this parameter is therefore used as a steering function in ecological models.In the case of ciliates it was demonstrated that temperature accelerates both ciliate growth (Müller & Geller 1993, Montagnes et al. 2003) and feeding rates (Dolan & Coates 1991), modifying energy flow through

a ciliate community. The aim of this study was to assess the dependence between the clearance rate of the common marine ciliate Balanion comatum Wulff 1919 and ambient temperature. B. comatum, redescribed by Jakobsen & Montagnes (1999), is a cosmopolitan marine ciliate. Decitabine in vivo Common both in coastal and offshore waters, also in the brackish Baltic Sea ( Witek 1998, Setälä & Kivi 2003), it grazes on nanoflagellates ( Jakobsen & Hansen 1997, Rychert 2008). Experiments were conducted under natural conditions with wheat starch added to water and used as a surrogate of food particles. Starch particles were observed inside ciliates after staining with Lugol’s solution. The volume of water cleared of starch particles (clearance rate, μl cell−1 h−1) was plotted against environmental temperature to check the statistical significance of the regression. The Q10 coefficient is most convenient for ecological modelling (e.g. Brush et al.

All tools developed for

All tools developed for Daporinad manufacturer the integration of omics data and their analyses will be made available on it. The first short-term objective of the HDPP project is to gather knowledge on diabetes and related complications already acquired by the different partners. Data on human islets, rodent beta-cells, and blood glycation are already accessible from partners’

research projects as described in this section. They will be grouped and further processed using bioinformatics tools to enhance current knowledge of key diabetes pathways. This first leveraged knowledge base will be further enhanced by integration of results from additional HDPP projects. The first deliverable for HDPP is to generate a list of proteins that are of central interest for the condition of diabetes. This list (supplementary data 1) was generated from the neXtProt database, by first searching this public domain with specific key words related to different subtypes of diabetes, and then by expert validation of the retrievals. The actual list comprises 1379 proteins, and will further evolve and mature over time. Each entry contains: the protein and gene names; the neXtProt/UniProtKB accession

number; the SRM/PeptideAtlas and Human Protein Atlas cross-references; a list of available protein binding reagents; the chromosome location; and the number of isoforms/variants/PTMs. This resource is already available on the HDPP website (www.HDPP.info). A proteomic analysis in the context of the Beta-JUDO Endonuclease project (see Section PLX4032 supplier 5.5) allowed the identification of more than 5300 human islet-related proteins by Gas-Phase Fractionation mass spectrometry. The resulting dataset has been submitted to PRIDE (27518-27529) via ProteomeXchange

(10.6019/PXD000050). Furthermore, this list was used by neXtProt to upgrade the protein existence level of some proteins. A brief overview of the identified proteins can be found in supplemental data 2. Each entry contains the same type of data than the 1000-HDPP list. The rat insulin-secreting cell line INS-1 was established in 1992 [24]. It is probably the most widely used clonal cell model in beta-cell research. Several proteomics datasets on total cell [25] and sub-cellular fractions [26] have been obtained from this slowing growing rat insulinoma beta-cell with more than 2500 identified proteins. The list is in supplementary data 3. Each entry contains the UniProtKB accession number, the name and the gene name. An analysis of glycated proteins in biological samples could give new insights into the characterization of the blood glycated proteome [27]. Therefore a qualitative/quantitative approach has been developed. Hyperglycaemia is a conditioning factor promoting the non-enzymatic glycation of proteins in those sites kinetically favored. The blood glycated proteome is dynamic and evolves qualitatively and quantitatively with unbalanced glucose concentration.

01) In contrast, comparing the effect of ATP depletion to that o

01). In contrast, comparing the effect of ATP depletion to that of BCRP inhibition ( Fig. 3B) showed that these two treatments caused similar changes to [3H]nifurtimox accumulation after 1, 2.5, 5 and 20 min, although it was noted that after 30 minutes ATP depletion caused a significantly greater increase (by 17–20%) in [3H]nifurtimox accumulation (p < 0.05). There

were no significant differences in [14C]sucrose accumulation between any treatments (data not shown). Probenecid (350 μM) was used to assess any initial contributions to [3H]nifurtimox and [14C]sucrose accumulation from proteins separate to P-gp and BCRP; namely multi-drug resistance associated this website proteins (MRP) 1 and 2, organic anion-transporting polypeptides (OATPs) and organic anion transporters (OATs) (Table 1). Fig. 4 illustrates

the time dependent effect of probenecid on [3H]nifurtimox accumulation. This was not matched by the presence of 10 μM indomethacin, where no significant change to [3H]nifurtimox was observed at any time point. Taurocholic acid (TCA, 200 μM) and para-aminohippuric acid (PAH, 500 μM) were then INCB018424 price used to assess function of OATPs and OATs respectively. The addition of TCA caused significant changes in [3H]nifurtimox accumulation from 2.5 min (p < 0.01) and onwards when all three time-points showed significant increases (p < 0.001 Fig. 3), albeit less than those observed with the BCRP inhibitors. PAH caused no significant differences in accumulation of [3H]nifurtimox at any time point. No significant differences in [14C]sucrose accumulation between any treatments were observed (data not shown). With

CTs becoming the treatments of choice for HAT, the effect of their addition to the accumulation buffer was observed on [3H]nifurtimox and [14C]sucrose accumulation. The accumulation of [3H]nifurtimox in the hCMEC/D3s was not significantly affected by unlabelled melarsoprol (30 μM), whereas unlabelled pentamidine (10 μM) caused an increase at 2.5 min (p < 0.01) and this was maintained onwards to 30 min (p < 0.001), in comparison to DMSO controls ( Fig. 5A). The effect MRIP of eflornithine (250 μM) and suramin (150 μM) on the accumulation of [3H]nifurtimox (without the presence of DMSO) saw no significant changes arise (Fig. 5B). There were no significant differences in [14C]sucrose accumulation between any of these treatments, or between DMSO and no DMSO controls (both [3H]nifurtimox and [14C]sucrose, data not shown). The potential of the compounds used in this study to cause cytotoxicity was assessed using an MTT assay and the effect compared to untreated control endothelial cells (hCMEC/D3) (Fig. 6). There were no significant differences on cell viability after 30 minutes exposure to the drugs, except when using the positive control 1% Triton X-100 (p < 0.01).

Each term will be a product of Ncyc individual FxByy factors, and

Each term will be a product of Ncyc individual FxByy factors, and

the sum is over all terms with the same frequency, Fkj. As the matrix multiplication depends on the order with which the matrices are multiplied, these factors are evaluated numerically in what follows. Neglecting chemical exchange during signal acquisition ( Supplementary Section 7), the overall ground state signal intensity obtained Sunitinib order after a CPMG experiment will be given by Eq. (8). Using a combination of Eqs. (8) and (61) the individual contribution of each frequency at a given k and j, to the overall signal of the observed ground state resonance can be calculated from: equation(63) Skj=IkjI(0)=Bkj(0,0)+Bkj(0,1)PEPGeFkj The individual term coefficients are shown in Fig. 4B for the given exchange parameters, Y-27632 price temporarily neglecting relaxation effects from the exponential term exp(Fkj). At higher pulsing frequencies therefore, the combinatorial factors inherent to the experiment considerably increase the influence of frequencies that correspond to mixtures of ground and excited state ensembles (Fig. 4A). When the relaxation inherent in the exponential term is included, the contribution from the terms that have spent more time on the excited state is heavily

attenuated, as f11R ≫ f00R ( Fig. 4C, terms higher up the y-axis). Nevertheless, as more frequency terms contribute to the signal ( Fig. 4C and D), and the observed intensity increases

( Fig. 4E) leading to the filipin characteristic form of the CPMG curve ( Fig. 4F). In summary, the combinatorial factors associated with pathway degeneracy ( Fig. 4A) tend to favour these terms as the fast pulsing limit is approached. This leads to magnetisation that would effectively have otherwise have decayed away to nothing in the low pulsing frequency, to instead be converted to observable signal ( Fig. 4E and F). As a consequence, faster pulsing leads to greater signal intensity over the same constant time. It is common to describe the action of the CPMG experiment in terms of its ability to refocus magnetisation. Here it is shown that this is an incomplete physical description. The CPMG experiment does tend to refocus chemical shift as expected, but it is only refocused magnetisation that spends the majority of its time in the ground state mixed ensemble (associated with the frequency f00) that relaxes sufficiently slowly to contribute significantly to the observed signal. At low pulsing frequencies, only magnetisation that remains with the ground state ensemble contributes significantly to signal intensity. By contrast, at higher pulsing frequencies, the ground and excited mixed-state ensembles are interconverted, enabling new pathways for magnetisation to follow.

The tidal currents may reach a speed of a few dm s−1 and dominate

The tidal currents may reach a speed of a few dm s−1 and dominate any other flow, the more so as they move the whole water column. They give rise to strong mixing of water masses, preventing thermohaline stratification in the shallow southern North Sea. In the Wadden Sea tides cause the periodic exposure of large areas of the sea bed. The shallow topography of the North Sea supports nonlinear effects caused by energy dissipation at the bottom and changing depths due to tidal waves. These processes are stronger than the nonlinearity due

check details to advection. As a result tidal curves and figures are severely non-harmonic. Averaging the tidal flow results in significant residual currents, which means a permanent displacement of water masses that is independent of any wind or density forcing (see Figure 9). This permanent flow system supports the cyclonic circulation

of the North Sea. It may be mentioned in passing that model calculations with a random forcing at the North Sea’s open boundaries yielded a similar system of residual currents (Günther Radach, personnal communication). Obviously, the specific topography of the North Sea together with nonlinear effects leads to a rectification of chaotic movements. Another example of nonlinearity is this website the superposition of the wind- and density-driven circulation on the tidal flow. Figure 10 shows the propagation of a wind surge in the North Sea with and without considering tidal interaction. The generation of secondary waves around the basin is strongly reduced by tidal dissipation. Backhaus et al. (1986) have shown that whenever Cepharanthine a constant flow component is combined with a time-dependent periodic tide, there is a considerable reduction in the resulting residual flow. They explained this process by the presence of a much higher energy dissipation due to bottom friction when the actual tide is included, compared to the linear superposition

of constant residual flow fields. In the following, the relevance of the fundamental oceanic forcing mechanisms (geostrophy, Ekman flow, Joint Effect of Baroclinicity and Relief JEBAR) for the North Sea will be examined. The numerical simulations are based on the Hamburg Shelf-Ocean Model HAMSOM, a three-dimensional, baroclinic circulation model with a free surface (Backhaus 1985). For details, see Sarkisyan & Sündermann (2009). Pohlmann (2003) extracted the baroclinic part υ_g=(υg,ug) of the geostrophic flow from the results of the complete circulation model HAMSOM. First, the temperature and salinity fields T  , S  (x  , y  , z  , t  ) were computed on the three-dimensional model grid, next the density ρ  (x  , y  , z  , t  ) was determined by the equation of state, and finally υ_g was calculated: υg(x,y,z,t)=gρf∂∂x(∫z0gρ(x,y,z′,t)dz′), ug(x,y,z,t)=−gρ0f∂∂x(∫z0gρ(x,y,z′,t)dz′),where g is the acceleration due to gravity, f is the Coriolis parameter and ρ0 is a reference density.

Further work on spatial typologies is currently being conducted w

Further work on spatial typologies is currently being conducted within the European Observation Network for Territorial Development and Cohesion (ESPON) which has recently funded projects compiling spatial typologies [13] and a project exploring European Seas Development

Opportunities and Risks (ESaTDOR) which includes the development of a maritime region typology [14]. This paper reports on the findings of a pilot study that was undertaken to test the development of a data informed spatial typology for the Baltic Sea. The Baltic Sea is a comparatively shallow sea with nine adjoining countries and intense anthropogenic activities. The area benefits from a large assortment of data on anthropogenic activities and environmental buy Veliparib conditions. The aim of

the study was to assess the applicability and value of such a spatial typology for MSP. The paper starts with a short pen picture of the study site covering its environmental, social and economic characteristics and the current status of MSP related activities in the region. This is then followed by an explanation of the methodology used in the typology development and an account of the study findings. The paper concludes with a discussion of key issues raised by the exercise and the implications for future typology check details development to promote more sophisticated and place sensitive approaches to MSP. The Baltic Sea is a semi-enclosed sea covering an area of approximately

387,000 km2[15]. Connections to other seas Neratinib molecular weight exist via the Danish Straits and Kiel Canal only. Limited inflows of saline water together with strong riverine freshwater inflows result in one of the world’s largest brackish water bodies. Salinity gradients from west to east and from south to north (e.g. surface salinities of 20 PSU in the Kattegat and 1–2 PSU in the northern Bothnian Bay) have led to a unique mix of marine and freshwater species, as well as to a few true brackish water species. At the same time the limited exchange of water results in water retention times of up to 30 years—along with the organic and inorganic matter it contains [16]. The Baltic Sea, which is home to more than 85 million people in its catchment area, is due to its geographical, climatological, and oceanographic characteristics highly sensitive to environmental impacts of human activities. This sea is comparatively small with only very few areas having a distance of more than 50 nm to the nearest coastline which facilitates a high density of anthropogenic activities. Entering or leaving the Baltic Sea 93,057 ships passed the two entrances Skaw and Kiel Canal in 2009 [17] and [18]. Estimations assume that more than 1.6 million leisure boats of all sizes are used [17].

Even when needs were expressed by relatives, they were not consid

Even when needs were expressed by relatives, they were not considered as a potential client “How can I put it? Even though I was sad, they did not ask why I was feeling that way…” (R25T2). There was a perception of inequality, of inconsistency in services received by relatives where those who were themselves (or a close one) part of the health care system were favored “I told them that my wife used to be a nurse, so maybe it played in PD0332991 datasheet my favor” (S14T2) or “I think it might have helped communication

with the social worker once they knew that she was also a social worker” (S15T1). Communication abilities of health professionals emerged as a key factor to foster respect and confidence toward health professionals “He gave me his hand, and he explained me this and that. I liked it when they introduced themselves” (R2T1) or “They were always available and always smiling all the time, as if we were not disturbing them, you know” (S1T1). Good communication between health professionals was appreciated but was perceived as a challenge in acute care settings “I would repeat in the evening, repeat over the next morning, I would repeat every hour, because I was there on a working shift, you know. You tell yourself ok, at some point,

I have other things to do. Always repeating…” (R4T1). Information-seeking on the part of relatives was perceived as being the norm “I tell you, it’s the same everywhere. Here [in rehabilitation] or in acute care, it’s just the same thing. If you want information, you have to run after it yourself, that’s all” (R23T2). As relatives needed to seek for services, availability selleck chemicals and attitudes of health professionals emerged as a determinant factor which was perceived as a facilitator when for example doctors would do systematic daily rounds “…we had a doctor who would

come almost every day. He took time to talk with us… he would come early in the morning or in the afternoon at around 3 pm” (S9T2) or when the physical environment was supportive “Yes, and MRIP of course we would pass by, we would walk around, and they were very close… on the ward, three doors away, and the physiotherapist and occupational therapist were there” (R1T2) or when there was a stability in personnel which was mentioned more frequently in the context of rehabilitation as compared to acute care “So we would walk by, and with time they would recognize us because it was always the same staff. And they would talk to us and ask how we were doing and all that” (R1T2). In contrast, barriers mentioned were high staff turnover “In the first few days, there was a lot of staff turnover, and it was difficult to get new information” (R10T1), scheduling issues such as personnel availability only during day time and weekdays (working hours) “…we did not really speak to the neurologist because he was working days, and we could not be there during the day” (R20T1) or “But you know, treatments were during the day.

, 2004), peptidoglycan ( Verbrugh et al , 1981) and lipoteichoic

, 2004), peptidoglycan ( Verbrugh et al., 1981) and lipoteichoic acid ( Wergeland et al., 1984), are also known to be immunogenic. In future studies we will include the analysis of the host response against these cell-wall components as well. Moreover, next to IgG levels, other immunoglobulins and their subclasses will be investigated. The authors do not have a commercial or other association that might pose a conflict of interest. We thank D.G.A.M. Koedijk for purification of Nuc, LytM, and IsaA. We thank G. Buist, T. Bosma, T. Foster, J.I. selleckchem Flock,

S. Rooijkakkers, S. Holtfreter, D. Grumann, and J.D. Fraser for kindly supplying the S. aureus proteins. S.v.d.B., T.B., G.B., J.M.v.D., A.v.B. and I.B.-W. were in part supported financially by the Top Institute Pharma project

T4-213. “
“Salmonella enterica causes a spectrum of diseases, including typhoid and paratyphoid fever, and gastroenteritis ( Everest et al., 2001, Hohmann, 2001 and Boyle et al., 2007), and is a major threat to public health. S. enterica Verteporfin order serovar Typhi is the causative agent of typhoid fever. Paratyphoid fever, a clinically-similar disease with less prevalence, is caused by S. enterica serovar Paratyphi A, B and C. In developed countries, nontyphoidal isolates of Salmonella (NTS) usually cause gastroenteritis. In Africa, NTS, especially S. enterica serovar Typhimurium, are a common cause of invasive disease, in particular bacteremia. NTS bacteremia in sub-Saharan Africa primarily occurs in children under 2 years of age and HIV-infected individuals ( Graham et al., 2000, Graham, 2002, Graham, 2010, Brent et al., 2006 and Bronzan et al., 2007). The estimated minimum incidence of NTS bacteremia is 175 per 100,000 in Kenyan children under 5 years of age

per year ( Berkley et al., 2005). The lack of specific clinical presentation of NTS bacteremia makes diagnosis difficult. In addition, increased drug resistance and the emergence of new multi-drug resistant isolates ( Hohmann, 2001 and Mirza et al., 1996) have added to the burden of this often fatal disease. These findings emphasize the need for an effective vaccine against NTS. Currently, none is available for use in humans. The role of antibody in protection against Linifanib (ABT-869) Salmonella has been well established. Adoptive transfer of antibodies confers protection against virulent Salmonella challenge ( Mastroeni et al., 1993 and McSorley and Jenkins, 2000). The importance of antibodies has also been emphasized by studies on Vi polysaccharide, which elicit T cell-independent antibody production and confer protection ( Acharya et al., 1987). A key assessment of most vaccines is their ability to induce specific antibody production. However, high antibody levels alone are insufficient, since vaccine-induced antibodies need to be protective.

Cells were centrifuged for 10 min at 10,000 x g and washed three

Cells were centrifuged for 10 min at 10,000 x g and washed three times in 0.85% (w/v) of NaCl. Then, a 10% aliquot was inoculated in MMFe medium (50 ml in 250-ml flasks) [13] with different concentrations of hydroquinone (Sigma-Aldrich, ReagentPlus™, ≥99%, Batch#:114K2623) (see “Results” section). Three replicates were used per test for each hydroquinone concentration. Uninoculated control flasks (duplicates) were incubated and aerated in parallel as negative controls

of the experiment. Hydroquinone concentration was monitored up to an incubation time of 96 h. Biosorption by dead biomass was determined by batch adsorption equilibrium experiments as follows. The strain P. chrysogenum var. halophenolicum was grown in the MC liquid medium

at 25 °C in a shaker incubator at 160 rpm Quizartinib nmr for 68 h. Mycelium pellets were separated from the growth medium by centrifugation and washed twice with NaCl solution (0.85% (w/v)). The biomass was sterilized for 15 min at 121 °C and 124 kPa to kill the fungus, preventing biodegradation and bioaccumulation Tanespimycin of hydroquinone in the subsequent adsorption experiments. The biomass was then rewashed with NaCl solution (0.85% (w/v)), centrifuged and approximately 50 ml of MMFe with 300 mg/l of hydroquinone were mixed with 0.10 g biomass (dry weight). The suspension was shaken at 25 °C in a rotary shaker at 160 rpm for 56 h, before the residual aqueous concentration of hydroquinone was measured by HPLC. Hydroquinone concentrations were quantified by High Performance Liquid Chromatography apparatus L-7100 (LaChrom HPLC System, Merck), equipped with a quaternary pump system, and L-7400 UV detector according to a previously published method [22]. Hydroquinone could be separated and concentrations

estimated within 10 min, using standard (Sigma-Aldrich, ReagentPlus™, ≥99%). The OxiTop® respirometric system (WTW, Germany) was used for assessing the biodegradability of hydroquinone over 5 days. The principle of the operation was based on the measurement of the pressure difference not in the closed system. During hydroquinone biodegradation the respiration increases, the produced CO2 was captured by an alkaline solution, and microbial oxygen consumption resulted in the subsequent pressure drop. All experiments were performed in reactors consisting of headspace and glass bottles (510 ml nominal volume) with a carbon dioxide trap (approximately 0.5 g of NaOH was added in each trap) with 97 ml of sample volume (MMFe with 5% of inoculum supplemented with 4541 and 7265 μM of hydroquinone). Fungal blanks were analyzed in parallel to correct for endogenous respiration. Respirometric analyses were conducted for 120 h in a temperature controlled chamber at 20 ± 1 °C and in the darkness. Decrease in headspace pressure inside the reactor was continuously and automatically recorded.