Relating spatial and temporal variability in sediment chlorophylla and carbohydrate distribution with erodibility of a tidal flat

Trends in the spatial distribution of chlorophylla (chla) and colloidal and total carbohydrates on the Molenplaat tidal flat in the Westerschelde estuary, Netherlands, reflected spatial differences in physical properties of the sediment. Results from a Spearman Rank Order Correlation indicated that many of the physical and biological measures covaried. Multiple regression analyses describing the relationship between colloidal carbohydrates and sediment properties resulted in several highly significant equations, although in all cases chla was able to predict colloidal carbohydrate content. Relationships between sediment surface chla and colloidal carbohydrate, and sediment erodibility (i.e., critical erosion threshold, U_crit, and mass of sediment eroded at a velocity of 30 cm s^?1) determined in annular flume experiments were examined. Overall sediment erodibility was lowest (i.e., high thresholds, low mass eroded) for the siltiest sediments in June 1996 when chla and colloidal carbohydrates were high (56.9 μg gDW^?1 and 320.6 μg gluc.equ. gDW^?1, respectively), and greatest (i.e., low thresholds, high mass eroded) at the sandier sediments in September 1996, when chla and colloidal carbohydrates were low (1.0 μg gDW^?1 and 5.7 μg gluc.equ. gDW^?1, respectively). When sediments were grouped according to relative silt content, the most significant relationships were found in muddy sand with a finegrained fraction (<63 μm) of 25–50%. Thresholds of erosion increased, while mass of sediment eroded decreased, with increasing chla and colloidal carbohydrate. A similar trend was observed for the sand-muddy sand (63 μm 10–25%). In the sand (63 μm 0–10%), there were no relationships for U_crit, whereas mass eroded appeared to increase with increasing chla and colloidal carbohydrate. The increased carbohydrate may stick sand grains together, altering the nature of erosion from rolling grains to clumps of resuspension.     

Chronologies of sedimentary changes in the south Bohai Sea,China: constraints from luminescence and radiocarbon dating

The alternation of terrestrial and marine deposits is an indicator of past environmental and sea‐level changes. The age of deposition is usually dated by means of radiocarbon. However, radiocarbon dates of molluscan shells from coastal areas may be complicated by various sources of carbon, and problematic for deposits of 40–50 ka or older. Herein, we apply the Optically Stimulated Luminescence (OSL) dating method to date samples from terrestrial and marine/coastal sediments extracted from three cores in the south Bohai Sea, China. Multiple‐ and single‐aliquot regenerative‐dose procedures using OSL signals from fine‐silt (4–11 μm), coarse‐silt (38–63 μm) and fine‐sand (63–90 or 90–125 μm) quartz were employed to determine the equivalent dose (D _e). The results showed that: (i) OSL ages from quartz of different grain sizes and different protocols are consistent with each other; (ii) for Holocene samples, most of the radiocarbon dates agree well with OSL ages; (iii) for pre‐Holocene samples, radiocarbon dates cluster at 40–50 ¹⁴ C ka BP, whereas OSL ages are in stratigraphic order from 11 ka to 176 ka. Because of the self‐consistency of the quartz OSL ages, the stratigraphic agreement in the three cores, and the clustering of the radiocarbon dates, we suggest that the quartz OSL ages are more reliable with respect to dating the samples from the south Bohai Sea. Finally, the four marine strata identified in the south Bohai Sea are likely to have formed during the Holocene, Marine Isotopic Stage (MIS) 3–5, MIS 6 and probably MIS 7, respectively.     

Reactivity of organic matter in aquifer sediments: geological and geochemical controls

Reduction rates in aquifers are commonly carbon limited, but little is known about the molecular composition and degradability of sedimentary organic matter (SOM) in aquifer sediments. The composition, source and degradation status of SOM in aquifer sediments of fluvio-glacial (Pleistocene) and shallow marine (Pliocene) origin, were determined using flash pyrolysis-gas chromatography/mass spectrometry. Incubation experiments (106 d) were used to assess the reactivity of SOM towards molecular oxygen. A dominance of lignin-derived components and long chain odd-over-even predominant alkanes indicate that terrestrial higher land plants were the main source of SOM even in the shallow marine sediments, while bacterial lipid-derived hopanoids and iso- and anteiso-C₁₅ and C₁₇ fatty acids indicate a minor contribution of microbial biomass. No compositional difference was observed between SOM present in the fine (<63 μm) and coarse fraction (63-2000 μm). A significant part of SOM was not present as low-molecular-weight compounds but was macromolecularly bound. For the fluvio-glacial sediments, a relatively higher abundance of resistant macromolecular compounds was in agreement with stronger signs of aerobic lignin, alkane and hopanoid oxidation. The more degraded status of SOM in the fluvio-glacial sediments was consistent with their significantly lower SOM mineralization (2-6%) during incubation, as compared with the shallow marine sediments (9-14%). The reactivity towards oxygen of SOM was controlled by the extent of past aerobic oxidation. Not the age of SOM, but the extent of oxygen exposure during syn- and postdepositional conditions seems most important in affecting the degradation status of SOM in aquifer sediments and thus their ability to reduce oxidants.     

Variability of dissolved organic carbon in sediments of a seagrass bed and an unvegetated area within an estuary in Southern Texas

Pore-water dissolved organic carbon (PWDOC) concentrations were examined in vegetated and bare sediments of aHalodule wrightii seagrass bed, and in a mud bottom sediment of a southern Texas estuary. Temporal variability was examined at diel (dawn and noon) and bimonthly time scales. Distribution patterns of PWDOC were compared with physical, chemical, and biological factors thought to exert control on PWDOC. Concentration of PWDOC, bacterial production, and resultant PWDOC turnover times displayed statistically significant spatial and temporal variability. Concentration of PWDOC ranged from 14 mg C 1^?1 to 107 mg C 1^?1 of pore water, or 9–71 μg C cm^?3 wet sediment. PWDOC was more variable and was approximately 5 times higher than DOC concentrations in the water column. Low PWDOC concentrations (mean = 14.6 μg C cm^?3) and high bacterial production rates (mean = 1.92 μg C cm^?3 h^?1) were observed at the mud station, whereas PWDOC concentrations were high (mean = 24.6 μg C cm^?3) and bacterial production rates were low (mean = 0.43 μg C cm^?3 h^?1) at the bare station. PWDOC turnover times (T_t), assuming 50% bacterial growth efficiency (1–840 h) were shortest at the mud station (mean=13 h) and longest at the bare station (mean=180 h). In the overlying water column, T_t values were longer, ranging from 1,000–10,000 h. PWDOC concentrations were 25% higher in vegetated sediments than in neighboring bare sediments. This difference was probably due to inputs of labile photosynthetic excretia, since bacterial production rates in vegetated sediments displayed significant diel variability and were 4 times greater than that of bare sediments. Based upon the entire data set, PWDOC was significantly related to macrofaunal biomass, sediment POC, sediment C:N ratios, and oxygen metabolism, but was significantly correlated only to the latter two variables in stepwise multiple regression. Our findings suggest that organism activities and detrital quality are the major determinants controlling variability in PWDOC.     

Adsorption of short-chain organic acids onto nearshore marine sediments

The adsorption of acetate, butyrate, lactate, and stearate was measured using a clastic mud from Cape Lookout Bight N.C. (CLB), a lateritic muddy sand from Kahana Stream, Oahu, Hawaii (KS), and a fine carbonate sand from Waimanalo Beach, Oahu, (WB). Partition coefficients (K_d, moles adsorbed per g of solid phase/moles dissolved per ml of porewater) ranged from 10^2.3 to ≤10^−3.0, and displayed the following trends: CLB > KS > WB, and stearate > acetate ∼- butyrate > lactate. The percent adsorption of the sediment organic acid pools showed similar trends: stearate, 99%; acetate, 9–23%; butyrate, 5–23%; lactate, ≤0.2–7%. These results reflected the relatively nonpolar nature of the sand surfaces in WB and KS sediments, and the polarities of the organic acids. K_d was approximately constant for each organic acid-sediment combination over a dissolved organic acid concentration range of 10⁷, using concentrations between 1M and 10⁻¹⁴ M. This constancy over a wide porewater concentration range suggested that adsorption was not limited by the availability of surface adsorption sites.     

Microbial lipids from a nearshore sediment from Bowling Green Bay,North Queensland: The fatty acid composition of intact lipid fractions

Samples from a sediment core collected in Bowling Green Bay, North Queensland have been analysed for hexane/isopropanol extractable lipids and fatty acids. These data revealed a subsurface lipid abundance maximum at 3–4 cm depth and consistent low total fatty acid abundances (ca 2 μg/g) in the deeper samples ( > 10 cm depth). Lipid phosphate was below the level of detection in all the samples. Bacterial community structure was found to vary markedly in the upper 10 cm of the core, with the 18:1Δ11 bacterial chemotype predominant in the surface sediment and trans-acid chemotypes dominating in the 3–4 cm depth sediment. Based on the fatty acid composition, the bacterial biomass was estimated to vary from 199 μg/g at 3–4 cm depth toca 8 μg/g at 11–13 cm depth, although the fatty acid distributions indicated possible interference from protozoan detritus. In order to test this possibility, a surface sediment sample from a nearby site was extracted and analysed for fatty acids in lipid fractions separated by silica column chromatography. The fatty acid distributions in lipid fractions containing wax/steryl esters, triacylglycerols, glycolipids and phospholipids were markedly different. These analyses were interpreted in terms of fatty acid contributions to the extractable lipids from bacteria, cyanobacteria, protozoan detritus and highly degraded organic matter.     

Geological characteristics of 2011 Japan tsunami sediments deposited along the coast of southwestern Mexico

The tsunami of 11th March 2011 was originated at the east coast of Japan and deposited ca.1 cm thick sediment layer along the coast of southwestern Mexico up to a maximum distance of 320 m from the beach. The sedimentological, mineralogical and geochemical characteristics of the sediments deposited during the tsunami (JT) are compared with the pre-tsunami sediments (PRT). JT sediments consist of dominant coarser fractions (>54% of medium to coarse sand), whereas PRT deposits comprise abundant finer fractions (>58% of fine sand). Assemblage of mafic and heavy minerals suggests similar provenance for both. The higher abundance and variation of heavy minerals along with higher concentrations of bromine (Br) and sodium (Na) in the JT deposits reveal the influence of high energy sea waves in transportation of heavy mineral rich coarse sediments onto the coastal lowlands.     

Small-scale spatial variation of macrobenthic community structure

Examination of small-scale spatial variation in essential to understanding the relationships between environmental factors and benthic community structure in estuaries. A sampling experiment was performed in October 1993 to measure infauna association with sediment composition and salinity gradients in Nueces Bay, Texas, USA. The bay was partitioned into four salinity zones and three sediment types. Higher densities of macrofaua, were found in sediments with greater sand content and in areas with higher salinity. High diversity was also associated with high homogeneous salinity (31–33‰) and greater sand content. Macrofauna biomass and diversity were positively correlated with bottom salinity, porewater salinity, and bottom dissolved inorganic nitrogen (DIN). Furthermore, species dominance shifted along the estuarine gradient.Streblospio benedicti dominated at lower salinity, but,Mediomatsus ambiseta andMulinia lateralis were the dominant species at higher salinity. Statistical analyses revealed significant correlations for sediment characteristics (i.e., increased fine sediments, water content, and total organic carbon) with decreased total abundance and diversity. Increased salinity and DIN were correlated with increased total biomass, diversity, and macrofauma community structure. These physico-chemical variables are regulated by freshwater inflow, so inflow is an important factor influencing macrofauna community structure by indirectly influencing the physico-chemical environment.     

Texture and geochemistry of the sediments of a tropical mangrove ecosystem,southwest coast of India

The textural and geochemical aspects of the sediments of a tropical mangrove ecosystem have been studied and discussed. The sediments are characterized by the abundance of silt and sand with minor amounts of clay. The mean size of the sediment ranges from 0.205 mm to 0.098 mm (fine to very fine grained sand). The sediments are very poorly sorted, negatively to very negatively skewed, and platy to extremely leptokurtic in nature. The organic carbon content of the sediments ranges from 0,33% to 4.93%, which is controlled by the particle size of the sediments. The CaCO₃ content is five times the enrichment of organic carbon. This enhanced CaCO₃ content of the mangrove sediments might be a result of the abundance of shell fragments in the sediments. The shell mining activities in the estuarine bed adjoining the Kumarakam mangroves also contribute a substantial amount of lime muds to the mangrove area, which in turn add CaCO₃ to the sediments. The relative concentrations of heavy metals are Fe > Mn > Cr > Zn > Ni > Cu. All heavy metals other than Fe show an increase in concentration compared to the other parts of the estuarine bed. Cluster analysis indicates that the contents of organic C, Fe and Mn have a marked bearing on the Cr, Zn, Ni, and Cu levels of the mangrove sediments.     

Bound carboxylic acids in the Alberta oil sands

The Alberta oil sands contain 1–2% organic solvent insoluble organic matter chemisorbed to the inorganic matrix. Analysis of the monocarboxylic fraction (1–14%) of the chemisorbed material has revealed the presence of C₁₂–C₃₂ normal, iso, anteiso alkenoic acids, mono and diunsaturated acids, cyclopropylalkanoic and cyclic terpenoid carboxylic acids. Some of the main components of the acyclic acids were similar to those which have been identified in various petroleums and Alberta oil sand bitumens (in small concentrations) by Mackenzie et al. (Advances in Organic Geochemistry 1981, pp 637–649, Wiley/Heyden, 1983), and attributed to bacterial degradation of the oils via the aerobic pathway of biosynthesis.The presence of these acids in the chemisorbed fraction and virtual absence in the bitumen lends additional support to earlier proposals that the Alberta oil sand bitumens have undergone severe microbial degradation.     

Water leaching and magnetic separation for decreasing the chloride level and upgrading the zinc content of EAF steelmaking baghouse dusts

Recycling scrap iron and steel in electric arc furnaces (EAFs) generates very fine metal-containing dusts which can present major environmental problems. This paper describes experimental work on a relatively novel, simple, and inexpensive process for decreasing the chloride content and upgrading the zinc level of dust from an Australian plant, to produce saleable products and environmentally safe waste products for disposal.The dust contained about 2.1% Cl as various chlorides, 23.1% Zn as zincite and franklinite, 27.1% Fe as magnetite, franklinite, and hematite, plus small quantities of lead, cadmium, chromium, and other materials. The dust was very fine (P₈₀ about 2 μm). Individual particles were commonly aggregates of fine spheres and other shapes.Simple water washing at ambient temperatures and natural pH (12) for 60 min extracted 99% of the chlorides, giving a residue assaying 200 ppm Cl. This residue was strongly coagulated by lime present in the dust and settled rapidly. The wash solution contained low levels of iron, zinc, lead, cadmium, and chromium, most of which could be removed by sulphide precipitation.Wet magnetic separation with a Davis tube was investigated. At the lowest field strength employed (0.6 A), 95% of the zinc was recovered in a non-magnetic product assaying 28% Zn and 24% Fe. At the highest field strength (1.6 A), 91% of the zinc was recovered in a non-magnetic product assaying 29% Zn and 25% Fe. Wet cycloning at a nominal separation size of 2–5 μm gave a cyclone overflow product assaying 31% Zn and 26% Fe, and containing 85% of the zinc. All these results fit a typical zinc grade–recovery relationship.The proposed process of water washing followed by magnetic separation or cycloning would produce a relatively high-zinc, low-iron, low-chloride product suitable for treatment in a lead–zinc smelter or electrolytic zinc plant, a high-iron, low-zinc product suitable for land fill, and a treated waste water for discharge to a sewer.     

Effect of fish and mesozooplankton manipulation on the phytoplankton community in the Patos Lagoon estuary,Southern Brazil

An enclosure experiment in the Patos Lagoon estuary, southern Brazil (32°S, 52°W) investigated the response of phytoplankton to the enhancement of mesozooplankton and fish abundance. Addition of nutrients (NO₃ ^? and PO₄ ^?) stimulated the growth of 3–20 μm diameter phytoplankton, especially the diatomCylindrotheca closterium, which, in turn, was heavily grazed by the dominant mesozooplankter, the copepodAcartia tonsa. Acartia did not consume small (2–3 μm) autotrophic flagellates and the cyanobacteriaAnabaena sp., despite their high cell number. Largest grazing ofC. closterium by the copepod occurred only after a decrease of ciliate abundance. The addition of mesozooplankton did not change the levels of primary production, but it significantly increased the phytoplankton assimilation number. Highest chlorophylla concentrations were measured in enclosures stocked with juveniles of the fishXenomelaniris brasiliensis. The large phytoplankton biomass and low mesozooplankton abundance found in this treatment indicates an, effective predator-mediated action on the phytoplankton community.     

Seasonality and abundance of ichthyoplankton in great South Bay,New York

The seasonality and abundance patterns of ichthyoplankton were investigated during 1985–1986 in Great South Bay, New York, USA. Eggs representing 17 species and larvae representing 23 species of fish were identified. Bay anchovy, Anchoa mitchilli, was the most abundant ichthyoplankter, comprising >96% of the eggs and >69% of the larvae collected. Bay anchovy spawned throughout the bay from late May through August, with peak baywide densities of >200 eggs and 6 larvae m^?3. Eggs of windowpane flounder (Scophthalmus aquosus) ranked second in abundance and were present in both spring and fall. Other dominant larvae were winter flounder (Pleuronectes americanus) and American sand lance (Ammodytes americanus). Their combined density reached 8 m^?3 and accounted for the winter peak in larvae. The seasonality of abundance of larval fish was strongly correlated with reported densities of copepod nauplii prey.     

Effect of grading characteristics on the undrained shear strength of sand: review with new evidences

In this paper, the shear strength of saturated pure sand and sand–silt mixture is evaluated by monotonic undrained triaxial tests that were carried out on reconstituted specimens at same relative densities and a constant confining pressure (σ ₃?=?300 kPa). The test results were used to conclude on the effect of low non-plastic contents (0–20 %) and grading characteristics on the liquefaction resistance of the sand. The test results indicate that the undrained residual strength reduced with the increase of non-plastic fine content. Also, shear strength of gap-graded sand mixed with low non-plastic fine content increases with decrease in effective size (D ₅₀). In other words, in this state, we can use the D ₅₀ as a parameter to control of silty sand’s undrained resistance. Besides, the undrained residual strength of pure sand specimens with same effective size increases due to increase of coefficient of uniformity (C _u).     

Sediment porewater sampling for metal analysis: A comparison of techniques

The concentrations of Ca, Mg, Fe, Mn, Cr, Co, Ni, Cu, Zn, Cd and organic carbon were measured in a sediment porewater sampled by two different techniques: in situ dialysis, and centrifugation followed by filtration. Sediment centrifugation at 5,000 rpm followed by filtration (0.45 μm membrane) was equivalent to dialysis for Co, Ni, Cr, Fe, Mn but gave higher and more variable concentrations for Cu, Zn and organic carbon. Concentrations comparable to those obtained by dialysis were found when centrifugation speed was increased to 11,000 rpm and when 0.2 or 0.03 μm membranes were used to filter the supernatant. This procedure was also found equivalent to dialysis for Cr, Co, Ni, Cd and organic carbon. A reduction of the dialysis membrane pore size to 0.002 μm did not produce any apparent change in the porewater composition; however, a further reduction to 0.001 μm indicated either incomplete equilibration after two weeks, or exclusion of medium sized metal-organic complexes. Because of its inherent simplicity, in situ dialysis appears particularly well adapted to the study of trace constituents in sediment porewaters under field conditions.     

The fractionation of a Recent sediment for organic geochemical analysis

A Recent unconsolidated lacustrine sediment was separated into five size fractions which were characterized by microscopy and XRD. Higher plant detritus predominated in the coarsest fractions, but decreased in proportion in the intermediate ones in which algal debris was predominant. The overall proportion of organic debris decreased from coarse to fine fractions. Quartz and feldspar were most abundant in the intermediate size fractions, while the coarsest fraction contained chlorite with some kaolinite and quartz, and the finest fraction was composed mainly of illite.Concentrations (per fraction dry weight) of solvent extract, total long chain hydrocarbons and total fatty acids decreased from coarse to fine fractions, with the exception of the finest fraction, in which they showed an increase. The change in relative abundance of higher plant to algal debris in the coarse and intermediate size fractions was paralleled by a decrease in the relative abundance of n-C₂₉ and n-C₃₁ alkanes and an increase in the relative abundance of -C₁₇ alkane. There was a progressive decrease in n-alkane carbon preference index, and a progressive increase in the unresolved envelope of hydrocarbons with decreasing grain size. The unresolved hydrocarbons, which probably originate from biodegraded lubricating oil, appear to be associated with the clay fraction. Fractionation in this way and lipid analysis of the separate fractions may give more definitive information about input sources than analysis of unfractionated sediments.     

Quantitative Zn speciation in a contaminated dredged sediment by μ-PIXE, μ-SXRF, EXAFS spectroscopy and principal component analysis

Dredging and disposal of sediments onto agricultural soils is a common practice in industrial and urban areas that can be hazardous to the environment when the sediments contain heavy metals. This chemical hazard can be assessed by evaluating the mobility and speciation of metals after sediment deposition. In this study, the speciation of Zn in the coarse (500 to 2000 μm) and fine (<2 μm) fractions of a contaminated sediment dredged from a ship canal in northern France and deposited on an agricultural soil was determined by physical analytical techniques on raw and chemically treated samples. Zn partitioning between coexisting mineral phases and its chemical associations were first determined by micro-particle-induced X-ray emission and micro-synchrotron-based X-ray radiation fluorescence. Zn-containing mineral species were then identified by X-ray diffraction and powder and polarized extended X-ray absorption fine structure spectroscopy (EXAFS). The number, nature, and proportion of Zn species were obtained by a coupled principal component analysis (PCA) and least squares fitting (LSF) procedure, applied herein for the first time to qualitatively (number and nature of species) and quantitatively (relative proportion of species) speciate a metal in a natural system.The coarse fraction consists of slag grains originating from nearby Zn smelters. In this fraction, Zn is primarily present as sphalerite (ZnS) and to a lesser extent as willemite (Zn₂SiO₄), Zn-containing ferric (oxyhydr)oxides, and zincite (ZnO). In the fine fraction, ZnS and Zn-containing Fe (oxyhydr)oxides are the major forms, and Zn-containing phyllosilicate is the minor species. Weathering of ZnS, Zn₂SiO₄, and ZnO under oxidizing conditions after the sediment disposal accounts for the uptake of Zn by Fe (oxyhydr)oxides and phyllosilicates. Two geochemical processes can explain the retention of Zn by secondary minerals: uptake on preexisting minerals and precipitation with dissolved Fe and Si. The second process likely occurs because dissolved Zn and Si are supersaturated with respect to Zn phyllosilicate. EXAFS spectroscopy, in combination with PCA and LSF, is shown to be a meaningful approach to quantitatively determining the speciation of trace elements in sediments and soils.     

Perylene occurrence,alkylation and possible sources in deep-ocean sediments

81 deep-ocean sediment samples obtained from the DSDP/IPOD program Legs 63–66, and six gravity-cores from DSDP/IPOD Leg 64 Guaymas Basin, Gulf of California, site survey cruise (SIO) were analyzed for perylene(s). Perylene was found to be most abundant in anoxic diatomaceous sediments containing moderate amounts of silts and/or clays. Elevated perylene yields, normalized to organic carbon contents, coincided with enhanced preservation of autochthonous tetraterpenoid and tetrapyrrole pigments, indicating a requirement of anoxia in the formation of perylene. Strongly euxinic conditions correlate with decreased perylene yields but not its total absence, as found for strongly aerobic deposition and/or redeposition. Perylene alkylation occurs in response to increasing in situ temperatures (alt. sub-bottom depth). This alkylation was found to begin with the generation of methyl (C-1) perylene and to eventually yield a perylene-alkyl perylene homologous series, in decreasing abundance, through the equivalent of C-3 (trimethyl, methyl-ethyl, propyl?) perylene. The realm of most intense perylene alkylation for Quaternary or Pliocene/ Miocene sediments corresponds with present in situ temperatures of 40–50°C or 30–35°C, respectively. Thus, the degree of perylene alkylation may represent an organic indicator for the thermal history of immature sediments. Geological phenomena, such as reworking and igneous intrusions, were found to complicate downhole perylene alkylation patterns. A substituted (-C₄H₇O₂) perylene was isolated from several anoxically deposited diatomaceous oozes and may represent one of the many possible perylene precursors. The possible source compounds and biota for sedimentary perylene are discussed in light of the present study and review of past reports.     

Patterns of rare earth and other trace elements in different size fractions of clays of Campanian–Maastrichtian deposits from the Portuguese western margin (Aveiro and Taveiro Formations)

The Upper Cretaceous (Campanian–Maastrichtian) Taveiro and Aveiro Formations belong to the northern sector of the Lusitanian basin (Portuguese western margin). The Taveiro Formation was deposited in alluvial fans, including mud flow beds, lakes and sinuous rivers. The Aveiro Formation was deposited in a flat region with low hydrodynamics channels, with the formation of a barrier island-tidal system. The reconstruction of this sedimentary basin may be difficult due to its complex architecture. This work aims a methodology to be used in the reconstruction of Cretaceous sedimentary environments of the Lusitanian basin, through the establishment of geochemical patterns of different size fractions of those deposits. Chemical analysis was performed by instrumental neutron activation analysis (INAA), and the mineralogical composition obtained by X-ray diffractometry (XRD). The whole rock and different size fractions (? ≥ 125 μm, 63–125 μm, 20–63 μm, 2–20 μm and ? < 2 μm) of selected samples were studied aiming the rare earth elements (REE) and other trace elements distribution and its correlation with the grain size and mineralogy.The results obtained for the studied Cretaceous sediments showed that REE patterns and other trace elements distribution in the different size fractions may be used as a tool to differentiate deposits within and between sedimentary formations. Within the Taveiro Formation, REE are concentrated in the silt fractions (20–63 μm and 2–20 μm) of the Reveles deposit, and in the clay size fraction of S. Pedro deposit, which is richer in kaolinite. The 1st transition elements, particularly Zn, are correlated with the presence of smectite in the clay fraction of Reveles deposit. In the sand and silt size fractions (>2 μm) of samples from Taveiro Formation correlations were found between: Ga and 1st transition elements, and phyllosilicates; Cs and mica; and Rb and Ba, and K–feldspars.The Bustos deposit (Aveiro Formation) samples are very fine-grained and with a high proportion of the fine silt fraction where REE are concentrated, especially the heavy ones. Incorporation of MREE, Co and U in carbonates of the coarser fraction appears to occur. The abundances of the 1st transition elements, Ga and As, are correlated with phyllosilicates.Significant differences were found in the trace elements patterns of the various analysed size fractions of the Lusitanian basin of Cretaceous sediments, between and even within formations, which can be used as a methodological approach for a fine paleogeographic reconstruction.