Distribution and ecological relevance of fine sediments in organic-enriched lagoons: the case study of the Cabras lagoon (Sardinia, Italy)

In organic-enriched sedimentary systems, like many Mediterranean coastal lagoons, a detailed analysis of sediment grain size composition and partitioning within the muds is crucial to investigate sedimentological trends related to both hydrodynamic energy and basin morphology. In these systems, sediment dynamics are particularly important because the partitioning and transport of fine sediments can strongly influence the redistribution and accumulation of large amounts of organic matter, and consequently the distribution of benthic assemblages and the trophic status and functioning of a lagoon. Nevertheless, studies on benthic-sediment relationships have been based mainly on a rather coarse analysis of sediment grain size features. In muddy systems, however, this approach may impede a proper evaluation of the relationships and effects of the distribution of fine sediment and organic matter on the biotic benthic components. Here we show that the distribution of sedimentary organic matter (OM) and total organic carbon (TOC) in the Cabras lagoon (Sardinia, Italy) can be explained (i.e., predicted) as a function of a nonlinear increase in the amount of the cohesive fraction of sediments (< or = 8 microm grain size particles) and that this fraction strongly influences the structure, composition and distribution of macrobenthic assemblages. Even in such a homogeneously muddy system, characterized by "naturally" occurring impoverished communities, impaired benthic assemblages were found at < or = 8 microm, OM, TOC contents of about 77%, 11% and 3.5%, respectively. A review of studies conducted in Mediterranean coastal lagoons highlighted a lack of direct integrated analysis of sediment features and the biotic components. We suggest that, especially in organic-enriched coastal lagoons, monitoring programs should primarily investigate and consider the cohesive fraction of sediments in order to allow a better assessment of benthic-sediment relationships and ecological quality of the system.     

Die chemische Zusammensetzung des Sestons in inneren Küstengewässern der DDR (Darß–Zingster Boddengewässer,südliche Ostsee)

Investigations were made on 27 seston samples of the years of 1978, 1979 and of the first half-year of 1982 from a station in the Zingster Strom. The mean contents – as mg/g dry matter – are: ash-free dry matter 569, C_total 284, C_inorg. 14, N_total 29, P_total 3.6, Fe_HCl-soluble 13. From them resulted the following weight quotients: C : N = 9.9 ± 2.4, C : P = 83 ± 21, N : P = 8.4 ± 1.8, Fe : P = 3.6 ± 1.0. The mean proportion of carbohydrate and the mean protein content amount to 170 and 180 mg/g, resp., dry matter. All parameters show pronounced dependences on seasonal and hydrographic situations, mainly the effects of wind on the very shallow water being of primary importance to the distribution and nature of seston.     

Effects of hydrological processes on the chemical composition of riverine suspended sediment in the Zhujiang River,China

The chemical composition of riverine suspended sediment is the integration of the weathering crust minerals, soil organic matter and erosion agency within a specific drainage basin, which has been largely disturbed by the human activities. Selected metal elements of the riverine suspended sediment in the Zhujiang River were analysed using inductively coupled plasma–atomic emission spectrometry (ICP–AES) in three different hydrological phases from 1997 to 1998 at Makou and Sanshui hydrographic gauge stations, located at the lower reaches of the two main tributaries of the Zhujiang River, i.e. the Xijiang and the Beijing Rivers respectively. Organic carbon and nitrogen were also analysed using a conventional element analyser. The results demonstrate that the chemical composition of the riverine suspended sediment show obvious variability in different hydrological phases, which closely correlate to the organic matter content in suspended sediment. Intensified erosion in the flood phase results in lower concentration of the organic matter than that in the lower water level phase. The riverine suspended sediment with rich organic matter in the lower water level phase adsorbs some metal elements from the river water. Copyright © 2003 John Wiley & Sons, Ltd.     

Organic geochemical studies of sinking particulate material in China sea area(I)

Sinking particulate material collected from Nansha Yongshu reef lagoon and the continental shelf of the East China Sea by sediment traps has been analyzed and studied for the first time using organic geochemical method. The results show that about half of the sinking particulate organic matter in the two study areas are consumed before reaching the depth of 5 m to the sea floor and the degree of this consumption in Yongshu reef lagoon is larger than that in the continental shelf of the East China Sea. The distributions of hydrocarbons and fatty acids indicate that the minor difference of biological sources of sinking particulate organic matter exists between Yongshu reef lagoon and the continental shelf of the East China Sea, but they mainly come from marine plankton. Stronger biological and biochemical transformations of sinking particulate organic matter are also observed and the intensity of this transformation in Yongshu reef lagoon is greater than that in the continental shelf of the East China Sea. It is found that the occurrence of C₂₅ highly branched isoprenoid (HBI) diene may be related to the composition of diatom species.     

武汉东湖沉积物中酸挥发性硫化物(AVS)的深度分布及其影响因素

提要沉积物中酸挥发性硫化物(AVS)是硫化物的生成、氧化和扩散等综合作用的反映,有机物的供给、硫酸盐的还原等因素都能影响其分布特征。本文对武汉东湖三个污染程度不同站点的AVS深度分布特征进行了研究,结果表明,AVS含量在一定深度沉积物中具有最大值,东湖沉积物中AVS的深度分布具有两种不同的模式,Ⅰ站和Ⅱ站AVS浓度峰在5cm左右的表层沉积物中,且AVS还原层深度较狭窄,而Ⅲ站AVS浓度峰处于10-20cm深度范围,沉积物中有机质负荷的差异是导致这种分布特征的重要原因。沉积物中有机质含量对AVS的深度分布具有重要影响,高有机质负荷导致AVS浓度峰向表层迁移,且AVS还原层分布于较狭窄的深度范围,对方涛等对流-扩散模型的应用表明,该模型在高有机质负荷沉积物中(Ⅰ、Ⅱ站)AVS深度分布的应用较为理想,然而低有机质负荷沉积物中(Ⅲ站)不能准确反映AVS的深度分布特征,说明其应用范围具有一定的局限性。     

Particle size characteristics of suspended and bed sediments in the rhône river

Ten large volume water samples were taken from the Rhône River (Switzerland-France) in November, 1989 for recovery of total suspended sediment by continuous flow centrifugation. the samples were freeze-dried and analysed for particle size, organic carbon, total nitrogen, and carbonate. for comparative purposes, four bed sediments collected in July, 1989 are also described. the Rhône can be subdivided into three sections on the basis of the origins of the water. the first section is the Upper Rhône River draining into Lake Geneva. Waters are derived from glaciers, with low temperature and conductivity and high turbidity. Suspended sediment is coarse, has a bimodal distribution, and is low in both organic matter and carbonate. the second reach is from Lake Geneva to the confluence with the Saône at Lyon and has warmer water with higher conductivity and very low turbidity. Suspended sediment is higher in organic matter, with high carbonate originating from the lake. the final section is from Lyon to Arles, with warmer water and higher conductivity and turbidity due to modification by the Saône. Sediment is rich in organic matter, which May, account for an observed decline in oxygen in the river waters downstream from Lyon. Carbonate in these sediments also decreases due to increased turbidity from the Saône. Suspended sediments other than from the Upper Rhône show a remarkable consistency in grain size, predominantly in the fine silts (mode 9-11 μm). This consistency indicates a high degree of suitability for geochemical analysis. Bed sediments were bimodal throughout, with a dominant coarse population in two out of the four samples. Grain size statistical parameters could be easily explained by application of the theory of mixing of two major populations in the sand size (bed traction load) and the fine silt/clay size (suspended sediment load).     

Chemical speciation of polycyclic aromatic hydrocarbons in sediments: Partitioning and extraction of humic substances

The primary objective of this study was to examine the chemical speciation of polycyclic aromatic hydrocarbons (PAHs) found in sediments endowed with different characteristics. To achieve this purpose and because the nature of the sediments influences the distribution of PAHs, we have analyzed four different types of sediments. To study the role of organic matter in the sequestration of PAHs, we fractionated humic substances into humic acids and humin-mineral fractions. After their separation and purification, the humic components were examined for their sorptive reactivity by extracting them with organic solvents; these extracts were subsequently subjected to GC/MS analysis. Our results show that PAHs are distributed between labile and sequestered fractions in sediments. A slower uptake of PAHs occurs when the sequestered fraction is formed, and this process can be prolonged and may be influenced by the characteristics if the sediment. Our study suggests that organic contaminants are available in muddy sediments for a longer period of time than in sandy sediments.     

Sulfate reduction using methane in sediments beneath a bathyal “cold seep” giant clam community off Hatsushima Island, Sagami Bay, Japan

Two sandy sediment cores (Cores D227-120 and D380) were collected from inside a deep-sea giant clam (Calyptogena soyoae) community off Hatsushima Island, western Sagami Bay, central Japan (35°59.9′N, 139°13.6′E; 1160 m deep) and a muddy sediment core (Core D227-202) was obtained from outside the community by the submersibleShinkai 2000. The chloride concentration of the pore waters is constant vertically and sulfate reduction using sedimentary organic matter occurs in Core D227-202 (21 cm long). The chloride concentrations are lower by 7% at the 7.5–9 cm depth in Core D227-120 (9 cm long) and by 3% at the 11–12 cm depth in Core D380 (16 cm long) than those of the overlying bottom waters in the cores from inside of the community. Sulfate concentration decreases remarkably and dissolved inorganic carbon, alkalinity, ammonium-N, and hydrogen sulfide concentrations increase significantly with increasing depth in Core D380.δ³⁴S values of sulfate ions increase from +20.5 to +35.3‰ andδ¹³C values of dissolved inorganic carbon decrease drastically from −7.0 to −45‰ with increasing depth from the top to the bottom of the core, although theδ¹³C values of the organic carbon of the sediments are−23.7 ± 0.9‰ in Core D380. These results indicate that sulfate reduction using methane is active within the sediments just beneath the living clams and that the hydrogen sulfide produced can be used by endosymbiotic sulfur oxidizing bacteria living in the gills ofC. soyoae in the community.     

Petrographische,mineralogische und chemische Untersuchungen an Sedimenten in den Deltabereichen von Schussen und Argen

Summary The influence of suspended matter from Argen and Schussen, two affluents to the Lake of Constance, on the mouth areas has been determined by means of sediment samples. The results of the granulometric analysis prove an evident primary division of the ground, which is disturbed by allochthone materials. With increasing amount of coarse-grained material the water content of the sediments is decreasing. Quartz, carbonates and feldspars predominate close to the mouth. With progressive distance from the mouth they are mixed and replaced more and more by clay minerals, coming from affluents of the vicinity too. According to these changes an increase of autochthone components (calcite) takes place. The results of the chemical analysis show a large-faced pollution of the sediments by organic matter. In contrast to carbon and nitrogen autochthone organic phosphorus is mineralized until the analytical limit. Therefore the C/P-relation oscillates with the station where the sediment sample has been taken, but the C/N-quotient is nearly constant. As a proof for pollution of the sediments by organic matter the determination of total-ammonium is adapted. A high concentration gradient exists between interstitial water and lake water. An exchange takes place mainly at areas with polluted sediments, because the density of the Tubificidae population here is high too.      

Spatiotemporal variations of deep-sea sediment components and their fluxes since the last glaciation in the northern South China Sea

Sediment components and their fluxes of Cores MD12-3428(water depth: 903 m), MD12-3433(water depth: 2125 m),and MD12-3434(water depth: 2995 m), obtained along a transect on the continental slope of the northern South China Sea, have been conducted to reveal the spatiotemporal variations and the controlling factors of the sediment components and of their fluxes.Results show that deep-sea sediments in the northern South China Sea are composed mainly of terrigenous(59–89%) and carbonate(6–38%) particles, with minor components of opal(1.6–9.4%) and organic matter(0.7–1.9%). Fluxes of terrigenous and carbonate particles reach up to 2.4–21.8 and 0.4–6.5 g cm–2 kyr–1, respectively, values that are one to two orders of magnitude higher than the fluxes of opal and organic matter. Temporal variations of the percentages and fluxes of deep-sea sediment components have displayed clear glacial-interglacial cyclicity since the last glaciation. Terrigenous, opal, and organic matter percentages and their fluxes increas clearly during marine isotope stage 2, while carbonate percentages and fluxes show an opposite variation pattern or are characterized by an unremarkable increase. This implies that deep-sea carbonate in the South China Sea is affected by the dilution of terrigenous inputs during the sea-level lowstand. With increasing water depth along the transect, the terrigenous percentage increases but with largely decreased fluxes. Both the percentage and flux of carbonate decrease, while the percentages and fluxes of opal and organic matter display much more complicated variational features. The spatiotemporal variations of deep-sea sediment components and of their fluxes since the last glaciation in the northern South China Sea are strongly controlled by sea-level fluctuations. Simultaneously, terrigenous supply associated with monsoonal rainfall, marine primary productivity,and the dilution effect between terrigenous and biogenic particles, also play interconnected roles in the sediment accumulation processes.     

Characterization of organic matter in marine sediments to estimate age offset of bulk radiocarbon dating

Radiocarbon dating of Arctic marine sediment is often challenging due to the low availability of calcareous fossils. Consequently, bulk organic matter dating has at times been used to establish sediment core chronologies. Yet, radiocarbon dates based on bulk organic matter often appear to deviate vastly from dates based on fossils, mainly caused by input of allochthounous carbon, including terrigenous organic matter. In this study, we aim to examine the link between the composition of the bulk organic matter and the age offsets between the bulk radiocarbon dates and those obtained from calcareous foraminiferal tests. All samples are taken from the marine sediment core AMD14-204C from offshore Upernavik (eastern Baffin Bay). The radiocarbon dates for bulk organic matter are on average ∼3000 years older than the radiocarbon dates based on foraminifera, but with changing age offsets throughout the record. To investigate the cause of this age offset and its variations over time, we applied core scanning, X-ray Fluorescence analysis, stable isotopes, organic pyrolysis and microscopic organic petrology to examine the distribution and characterization of the organic matter. The results show that the older organic matter includes clastic input of reworked sedimentary rocks potentially originating from West Greenland and/or the Canadian Arctic Archipelago. Changes in the input of contemporary marine algal produced organic matter versus both terrigenous input and reworked ancient organic matter appear to control the age offsets between the bulk and foraminifera dates. A low Hydrogen Index and low δ¹³C_org values together with a high Oxygen Index, indicative of high influence of terrigenous organic matter, seem to correspond to samples with the largest age offsets; 1000–2000 years greater than in other samples. To examine the cause of the variations in the age offsets, a new quantification of the autochthonous organic matter as a fraction of the TOC was calculated. This shows that samples with the largest age offsets contained the lowest fraction (as low as ∼12%) of autochthonous organic matter in the TOC.     

The geomorphic dynamics and environmental history of an upper deltaic floodplain tract in the Sacramento–San Joaquin Delta,California, USA

A multi‐proxy approach was used to examine the geomorphic dynamics and environmental history of an upper deltaic ?oodplain tract in the Sacramento–San Joaquin Delta, California. Three long cores were collected from the McCormack–Williamson Tract (MWT) and these cores were analyzed for bulk density, loss‐on‐ignition, ?ne (clay and silt) content, Al concentration, magnetic susceptibility, pollen, and charcoal. Radiocarbon dates obtained for the cores were converted into calendar years and an age–depth model was constructed. Long‐term vertical accretion and sedimentation rates were estimated from the age–depth model. Cross‐core relations show that coarse sediment generally accumulates more rapidly and has greater magnetic susceptibility compared to ?ne sediment. Percentage ?ne and LOI data show a strong linear relationship that indicates ?ooding is the primary mechanism for the deposition of particular organic matter on the ?oodplain and that landscape wash load has contributed a highly consistent fraction of persistent organic matter averaging 5·5 per cent to the site. Down‐core grain size pro?les show two hydrological domains in the cores, namely millennial ?ne–coarse ?uctuations superimposed on general up‐core ?ning. Coarse sediment is viewed as channel or near‐channel overbank deposits, whereas ?ne deposits are considered to be distal overbank ?ood deposits. The coarse–?ne ?uctuations are indicative of changing depositional settings as channels migrated laterally across MWT, whereas the upward ?ning trend re?ects a combination of self‐limiting overbank deposition as ?oodplain elevation increased and decreasing competence as sea‐level rise reduced ?ood‐pulse energy slopes. MWT has been cross‐cut and incised numerous times in the past, only to have the channels abandoned and subsequently ?lled by ?ne sediment. The channels around MWT attained their modern con?guration about 4000 years ago. MWT likely came under tidal in?uence at about 2500 cal BP. Wetlands have recently developed on MWT, but they are inorganic sediment dominated. Copyright © 2004 John Wiley & Sons, Ltd.     

氧化还原条件对红枫湖沉积物磷释放影响的微尺度分析

选取贵州红枫湖为研究对象,在实验室条件下模拟了自然、好氧和厌氧条件下沉积物内源磷的释放过程,联合应用微电极技术和沉积物磷形态分析对沉积物—水界面开展了微尺度观测与研究.结果表明,厌氧条件下红枫湖沉积物总磷含量显著降低,且主要是NaOH提取态磷(NaOH-P)和残渣态磷(rest-P)含量降低所致,厌氧条件下沉积物孔隙水中磷酸盐浓度明显升高,而好氧条件下沉积物孔隙水磷酸盐浓度显著降低,反映厌氧条件显著促进了红枫湖沉积物磷释放.厌氧条件下沉积物内部溶解氧浓度下降、硫还原活动增强可能是导致NaOH-P释放的主要原因.O_2浓度的降低加速了沉积物还原作用并产生大量H2S,进而与二价铁离子形成硫化亚铁沉淀,最终导致NaOH-P(Fe-P)释放到孔隙水中.好氧条件向厌氧条件的转换可通过改变沉积物内部pH值分布和微生物活动促使rest-P释放:厌氧条件下,厌氧微生物不仅可以消耗硫酸根产生H_2S,导致pH值降低,还可消耗有机质,将有机磷转变为无机磷.上述研究结果表明,沉积物—水界面氧化还原环境可影响沉积物氧渗透深度、pH值分布、微生物活动、硫循环以及有机质降解过程,进而控制沉积物磷的形态转化与释放.联合应用微电极技术和沉积物磷形态分析对湖泊沉积物—水界面开展微尺度观测研究是揭示沉积物内源磷释放机制与控制因素的有效途径.     

The effects of sewage organic matter on biogeochemical processes within mid-shelf sediments offshore Sydney, Australia

A laboratory incubation experiment was conducted using replicate cores collected from a muddy-sand sediment facies offshore Sydney, Australia to determine what components and processes would be affected by the addition of sewage organic matter. Sewage effluent has a solid phase composition of 40% carbon (35% organic carbon), 5% nitrogen, 1% phosphorus and 5% silicate. The molecular C:N:P ratio is 92:10:1, compared to the Redfield ratio of 106:16:1 in marine phytoplankton. Sediment cores were incubated at in situ temperature in a darkened room for periods up to 95 days. Sewage organic matter was added to the cores at three different loads equivalent to 0 (T0), 65 (T1) and 130 (T2) g m⁻² of sediment. Following the addition of sewage organic matter, fluxes of oxygen (into the sediments), ammonia and phosphate (from the sediments) increased, reflecting an enhanced organic carbon supply to the sediments. Oxygen penetrated to a depth of 6 mm in the ambient cores, but the sediment oxygen content was severely depleted following the addition of the sewage-derived organic matter. Sediment porewater data, together with nutrient flux data indicate that oxygen reduction, nitrate reduction and sulphate reduction occurs within these sediments. Following the addition of sewage organic matter, increases in total nitrogen, total phosphate and total organic carbon were measured to depths of 5 cm in the sediments, suggesting that bioturbation influences nutrient and organic carbon distributions. Additionally, irrigation of the surficial sediments may play an important role in the metabolism of organic matter. These results indicate that oxygen penetration, oxygen fluxes, nitrate concentrations within porewaters, ammonia flux rates, and solid phase concentrations of total organic carbon and nutrients may be useful indicators of sediments affected by high rates of organic matter deposition onto Sydney's offshore sediments. The EPA has recently predicted maximum deposition rates of sewage particulate matter to be approximately 1 g m⁻² day⁻¹. Because of the similarities in CNP ratios of sewage organic matter and marine organic matter, the effects of sewage organic matter and marine organic matter inputs to coastal sediments may not be easily distinguishable.     

Quantitative changes in sedimentary chlorophyll in the bed sediment of the Mikolajki Lake during the post-glacial period

Summary The thickness of the bed sediment 5·70 m of the Mikolajki Lake (Central Mazur District) was measured at a depth of 18·5 m by means of a vertical core sampler. In the samples taken from this profile the amount of sedimentary chlorophyll in relation to the dry mass of the sediment, the percentage of organic matter content and the absolute water content were determined. From analyses of the amount of sedimentary chlorophyll and organic matter in the Mikolajki Lake sediment, two stages in the development of the lake during the post-glacial period were distinguished which in their general outline corresponded to the climatic changes described byBlytt andSernander. During the periods when the climate was cold and humid the proportion of sedimentary chlorophyll and organic matter was smaller than during the periods of dry and warm climatic conditions when the lakes frequently became, for example during the boreal period. In addition, the author suggests that two layers originating from the humid period and two layers from the dry periods may be distinguished in the upper part of the profile. The former two would seem to correspond to the subatlantic period, the two latter to the neoboreal period.     

Untersuchungen zum Schadstoffpotential von Wasserwerksschlämmen

Investigation on the Pollution Potential of Waterworks Sludges Several contaminated sludges from water treatment plants with known or estimated concentrations of trace elements were investigated for their leaching characteristics and long-term stability using standard and advanced test procedures. Potentially hazardous elements in the sludge are zinc, nickel, and arsenic with concentrations of up to 1.2 g/kg dry matter (mass). Preliminary sorption tests with synthetic sludge components like iron hydroxide, manganese oxide, silicate clay minerals, and chitine powder as a model organic component showed that Cu is associated with the organic phase wheras arsenic is predominantly bound to the iron oxide minerals. The recently suggested pH_stat test procedure was used to assess the leaching characteristics of metals at typical pH values. This procedure was compared with the DEV-S4 test, the current standard test in Germany, consisting of a simple lixiviation of the solids with water, without pH control. The pH_stat test yields results which are much better to interprete than those obtained by the DEV-S4 procedure. The iron and manganese sludges are well buffered against changes in pH and redox potential so that low pH values and/or reducing conditions can hardly occur. Thus, in deposited material a sudden leaching of heavy metals is unlikely and due to the presence of iron and manganese oxides the pentavalent arsenic is protected against conversion into the highly mobile trivalent form at neutral to low pH. Co-deposition with reducing organic matter and alkaline stabilisation material or waste (like fly ash) could influence the binding properties and should be strictly avoided.     

Chemical characterization of porewaters in an intertidal mudflat of the Seine estuary: relationship to erosion-deposition cycles

A seasonal field study was carried out in the Seine estuary to determine the chemistry of sediment porewaters using the 'peeper' technique and changes in the elevation of the mudflats using the 'Altus' technique. This approach allowed us to evaluate the release of nutrients and to link these releases to the sediment hydrodynamics. Our results show that nutrient and organic matter cycling in a Seine estuary mudflat exhibits a seasonal behaviour, which is mainly influenced by variations in hydrodynamics. Sediments, rich organic matter, were input during floods and they were mineralized during summer and autumn, releasing nutrients and dissolved organic carbon into the sediment porewaters. The nutrient release, including ammonium, is mainly linked to the mineralization of organic matter, while the release of phosphate is delayed. The delay could be the result of phosphate association with organic matter and/or its co-precipitation with calcium and iron.     

Research on preservation and enrichment mechanisms of organic matter in muddy sediment and mudstone

Using multidiscipline methodologies, the differences in preservation and enrichment mechanisms of organic matter (OM) in muddy sediment and mudstone are investigated. In clay fractions, concentra- tions of TOC and chloroform bitumen “A” are significantly higher than those in coarser fractions. This indicates that clay minerals (CM) play an important role in enriching OM. The content of chloroform bitumen “A” increases obviously in the clay fraction, which reveals that dissolvable OM is the main composition of coalesce with clay minerals. Furthermore, TG and DTA data show that OM enrichment mechanisms and preservation forms have multiplicity. Several exothermic peaks in the DTA curves demonstrate that muddy sediment and mudstone contain a number of bioclasts and amorphous OM besides dissolvable OM. Through analyzing with XRD and DTA after mudstone samples were pretreated, the conclusions can be arrived at. Firstly, CM interlayer space of XRD curves and exothermic peaks of DTA curves both change as temperature increases. Secondly, the changes of CM interlayer space and exothermic peaks are concordant and stable around 350℃. All these are the features that OM enters CM interlayers to form stable organo-clay complexes. Therefore, the combination format of OM with CM is not only surface adsorption, partial OM enters CM interlayers to form stable organo-clay complexes. Finally, through the research on OM preservation forms and enrichment mechanisms in muddy sedi- ment and mudstone, the hydrocarbon-generation processes and the global carbon cycle and budget can be explained.