Environmental controls on branched tetraether lipid distributions in tropical East African lake sediments

Quantifying past continental temperature changes is an important aspect of paleoclimate research as it allows us to constrain the amplitude of natural variability, test predictive climate models, and provide a proper context for changes that may arise in response to anthropogenically-induced climate change. The recently developed biomarker-based methylation index of branched tetraethers/cyclization ratio of branched tetraethers (MBT/CBT) proxy shows potential as a new method for continental temperature reconstruction, but thus far it has only been applied successfully in ocean margin sediments. To assess whether this proxy is also applicable to the sedimentary record in tropical lacustrine systems, we investigated the distribution of branched glycerol dialkyl glycerol tetraethers (GDGTs) in recently deposited sediments from 46 lakes in tropical East Africa. These lakes span a substantial range in surface elevation (770-4500 m above sea level), and thus also a wide gradient of mean annual temperature. We find that, saline lakes excepted, branched GDGTs are universally abundant in the lakes investigated and can be used to predict mean annual air temperature (MAAT) with a high degree of accuracy. However, the existing global MBT/CBT calibration for MAAT based on soils predicts inaccurate temperatures when applied to our African lake dataset. This observation, together with the fact that surface water pH, and to lesser extent, lake depth appear to influence the distribution of branched GDGTs among sites, leads us to conclude that in situ production of branched GDGTs in lakes is likely. The robust relationship between branched GDGT distribution and the temperature and pH of African freshwater lakes makes these compounds suitable for paleoenvironmental reconstruction, however we urge caution in using branched GDGTs in lake sediments to infer past temperatures, unless their exact origin can be determined.     

Spatial variations and distributions of phosphorus and nitrogen in bottom sediments from a typical north-temperate lake,China

Concentrations and vertical distributions of total nitrogen (TN), total phosphorus (TP) and their different forms in sediments obtained from nine locations of Lake Dalinouer in September 2008 were analyzed. The results demonstrated that TP in surface sediments ranged from 0.493 to 0.904 g/kg, and inorganic phosphorus was the main fraction of total phosphorus, ranging from 335 to 738 mg/kg. Simultaneously, the autogenetic calcium phosphorus (ACa-P) was the main fraction of inorganic phosphorus, ranging from 145.4 to 543.2 mg/kg. Vertical distribution of different phosphorus forms in different sediment cores was distinguishing, and most of them tended to increase toward the surface sediment, indicated that the phosphorus concentration was related to the humanity with a certain extent. The relationships between TP and occluded phosphorus and ACa-P were significant. Nitrogen in the sediment was composed mainly of organic nitrogen, accounting for grater than 80 % of TN. NO₃ ^?-N was the dominate fraction of inorganic nitrogen in the surface sediment, ranging between 51 and 346 mg/kg (151.1 ± 104.4 mg/kg), and accounting for between 2.2 and 17.7 % of total sediment nitrogen (6.2 ± 5.6 %). The ratio of organic carbon and TN in sediment was in range of 6.0–25.8 and presented a tendency of lake centre >lake sides, indicating that nitrogen accumulated in the sediments from lake sides came mainly from terrestrial source and nitrogen was mainly autogenetic in lake centre. Ratio of N:P in all sampling sites was below 14, indicated that N was the limiting nutrient for algal growth in this lake.     

The use of magnetic measurements to investigate the mineralogy of Icelandic lake sediments and to study catchment processes

Magnetic measurements made on sediment and catchment samples from two contrasting Icelandic lakes show how susceptibility and saturation isothermal remanent magnetisation alter as magnetic minerals pass from rock to soil to stream and into the lakes. There is no detectable growth of secondary magnetic minerals in Icelandic soil profiles and susceptibility peaks in the 62.5–1000 μm size range of mineral particles in the lake sediments. Changes in sediment source can be detected using combinations of magnetic measurements.     

Holocene variations in the Asian monsoon inferred from the geochemistry of lake sediments in central Tibet

We present a record of monsoon variations for the early and middle Holocene that is inferred from the geochemistry of sediment cores from Ahung Co, a lake in central Tibet. The resolution of this record is better than 50 yr and the age model is derived from radiocarbon ages of terrestrial charcoal, which eliminates errors associated with the lake hard-water effect. We made down-core geochemical measurements of % carbonate, % organic carbon, C/N and δ¹³C of bulk organic matter, δ¹³C and δ¹⁸O of carbonate, and % dolomite. Proxy calibration and modern water-balance reconstruction show that these are proxies for lake depth and the amount of monsoon precipitation. We find that lake level and monsoon precipitation have been decreasing at Ahung Co since the early Holocene (∼7500 cal yr B.P.). Superimposed on this trend are rapid declines in monsoon rainfall at 7000-7500 and 4700 cal yr B.P. and seven century-scale wet-dry oscillations. The cores do not contain sediment from the last ∼4000 yr. Surface sediments from the lake accumulated during the 20th century, however. From this, we argue that lake levels have risen again recently following a late Holocene dry period.     

Salinity control on long-chain alkenone distributions in lake surface waters and sediments of the northern Qinghai-Tibetan Plateau, China

Long-chain alkenones in lacustrine settings are potentially excellent biomarkers for the reconstruction of past terrestrial environmental conditions, and have been found in many different types of lakes around the globe. A wider range of factors influence the occurrence and distribution of alkenones in lake sediments and waters when compared to marine systems. Lake environmental conditions, such as temperature (in particular) and salinity, are among the key factors controlling alkenone distributions in lacustrine settings. Here we investigated alkenone distribution patterns in lakes of the northern Qinghai-Tibetan Plateau, China, and their possible relationship with environmental conditions, by analyzing paired samples of suspended particulate matter in surface waters and surface sediments. Salinity of investigated lake waters ranges from almost 0 to ∼100 g/L, while temperature variation among the lakes is minimal, effectively eliminating temperature effects on the alkenone distribution patterns observed here. We show that (1) alkenone concentrations vary substantially between the lakes, yet controlling mechanisms remain elusive; (2) C₃₇/C₃₈ ratios are substantially lower in the lakes of the Qaidam Basin than in the Lake Qinghai region, probably indicating different alkenone producers in the two regions; and (3) large variations in %C_37:4 (the percentage of the C_37:4 alkenone), determined from both surface waters and sediments, are negatively correlated with salinity. We suggest that the %C_37:4 index could be used as a salinity indicator at least on a regional scale, with careful considerations of other potentially complicating factors. However, potential reasons for why salinity could significantly affect %C_37:4 values need further investigation.     

Six thousand years of records of metal mining and utilization from lake sediments in central China

A sediment core from the Liangzhi Lake, Hubei Province in central China, was used to assess metal usage and accumulation in the past 6000＋ years in China. The concentrations of trace metals, including Cr, Cu, Pb, Ni and Zn, and major elements, Ca, Fe and Mg, in the ^14C-dated sediment core were analyzed. Historical trends of metal inputs to the Liangzhi Lake from 5000 B.C. to the present were recorded in the sediments, representing over 6000 years of metal mining and utilization history in China. The concentrations of Cu, Ni, Pb and Zn have increased gradually since 3000 B.C., indicating the start of the Bronze Age era in ancient China, until the period 467-76 B.C. During the period of 467-76 B.C., there had been a rapid increase in the concentrations of these metals in the sediments, indicating the enormous inputs of these metals at that time. This era corresponded well with the Warring States Period （475-221 B.C.） and early Hart Dynasty （206 B.C.-220 A.D.） of China, during which copper and lead were extensively used in making bronze articles, such as vessels, tools and weapons. During 1876 A.D. to the early 1900s, there was also a significant increase in the metal concentrations, such as Cu, Ni and Pb, which could probably reflect the impact of metal emissions during the early industrial development and wars in China. The Pb isotopic analysis showed that the surface and subsurface sediments had lower ^206Pb/^207Pb, and ^208Pb/^207Pb ratios than the deeper layers, affected by mining activities both during the Bronze Age era and modem times.     

Petrochemistry of crater facies Tokapal kimberlite pipe, Bastar craton, central India and its orangeitic affinities

Tokapal kimberlite is the only well preserved crater facies kimberlite intruded within sedimentary sequence of Indravati basin in Bastar craton of central India. We present detailed petrographical and whole rock geochemical studies, carried out on ten samples collected from different locations from Tokapal kimberlite to constrain its genesis and also the mantle processes involved in the origin of this earlier characterized Group I kimberlite. Geochemical studies show that only SiO₂ content and the mobile trace elements Ba, Sr, and K vary in the crater facies while rest others show restricted range and can be successfully used in evaluating the petrogenetic processes. Very low abundances of Rb (<2 ppm), Sr (<28 ppm), Ba (<52 ppm) and Cs (0.02–3 ppm) are observed which show possible effects of late-stage alteration rather than significant crustal contamination. The LREE enriched REE pattern, absence of positive Eu anomalies and HREE depletion also provide further additional evidence against crustal contamination considerably modifying magma composition. We infer the presence of less enriched (metasomatised) mantle source regions and comparatively greater degrees of partial melting responsible for the genesis of Tokapal kimberlite. Present study also suggests that crater facies Tokapal kimberlite intruding the Indravati basin, Bastar craton has a Group II kimberlite (orangeite) affinity. This finding is important in light of recent identification of Mainpur kimberlites of Bastar craton as orangeites.     

Palaeoenvironmental history of the Holocene volcanic crater lake Lago d'Averno (central southern Italy) inferred from aquatic mollusc deposits

The mollusc record from Lago d'Averno, central southern Italy, provides a detailed 1600‐yr record of changes in water quality in response to bradyseismic movements and salinity fluctuations. Bradyseismic vertical land movements and human impact in Roman times led to several transgressions from the Mediterranean Sea, 1 km distant, making the lake a valuable resource for documenting the effect of episodic marine transgressions of a freshwater lake. Low‐oxygen‐tolerant freshwater molluscs suggest that, at around 900–500 bc the lake had a slowly decreasing medium freshwater quality, resulting from contamination of volcanic origin. Disappearance of the obligate freshwater snails and transgression of low‐salinity‐tolerant marine species indicate that, after 500 bc, continuous subsidence resulted in episodic marine transgressions from the nearby sea. The construction of a canal that connected the lake with the sea, in 37 bc, is marked by a considerable increase in the number of shells and by arrival of brackish‐water‐intolerant marine species. Species diversity increased considerably when the area was partly depopulated towards the end of the Roman Empire around ad 400. When the land was slightly uplifted around ad 600–750, the water quality of the lake became less favourable for marine molluscs. Copyright © 2000 John Wiley & Sons, Ltd.     

Magnetic properties of lake sediments from Lake Chalco,central Mexico,and their palaeoenvironmental implications

Lake Chalco (99.0°W, 19.5°N) in the Basin of Mexico, was formed during the Pleistocene after the emplacement of the Chichinautzin volcanic field that closed the former drainage system. The lake sediment record has been influenced by a number of factors, including glacial–interglacial cycles, local volcanism, erosion of soils and anthropogenic disturbances. The magnetic properties of the lake sediments and the associated tephra layers of the last 16500 yr have been studied. It is found that the magnetic properties of the Lake Chalco sediments are very distinctive. Magnetic concentration varies by a factor of 1000 and magnetic stability also varies over an extremely wide range. The predominant magnetic mineral is titanomagnetite in addition to an imperfect antiferromagnetic phase, possibly goethite. An unusually large range of coercivities is found in certain of the tephras. Down‐core variations in magnetic properties closely follow climatic/environmental changes previously established by other proxy methods. The late Pleistocene and late Holocene lake sediments display a higher concentration of magnetic minerals than the early–middle Holocene sediments. In the non‐volcanic sediments, fluctuations in the magnetic concentration reflect changes in both the intensity of erosion, as represented by ferrimagnetic and paramagnetic minerals, and by the maturing of soils, as represented by geothite. Copyright © 2000 John Wiley & Sons, Ltd.     

Assessment of heavy metal pollution in lake sediments of Katedan Industrial Development Area,Hyderabad, India

Spatial distribution and temporal trends studies were carried out at Katedan Industrial Development Area (KIDA) near Hyderabad, capital of Andhra Pradesh state, India under Indo-Norwegian Institutional Cooperation Program, to find out the extent of contamination in streams and lake sediments from the discharge of industrial effluents. Stream and lake sediment samples were collected from the five lakes in the study area and connecting water streams. The samples were analyzed by XRF spectrometer for toxic elements. The studies reveal that the stream sediments with in the KIDA and the impounded Noor Mohammed Lake down stream have high concentration of some of the toxic elements like chromium, nickel, lead, arsenic, zinc etc. The geology of the area indicates that the study area consists of residual soil of acidic rocks, which are predominantly of Archaean gneisses and granites having low to medium concentrations of chromium and nickel. The source of these high concentration of elements like lead 2,300 mg/kg, copper 1,500 mg/kg, arsenic 500 mg/kg, chromium 500 mg/kg etc. cannot be derived from the surrounding acidic rocks and may be attributed to the industrial effluents released in the ditches and random dumping of hazardous solid waste. It was observed that the metal concentrations increased in the streams during the dry season (pre-monsoon period). After the monsoon rains, the metal concentrations in the streams were reduced by half which may be due to dilution. The eroded sediments are deposited in the lake where very high concentrations were encountered. Overflowing of the lake will spread the contamination further downstream. The lake sediments will remain as a major source of contamination by desorption to the water phase regardless of what happens to the effluent discharge in the KIDA. However, some samples showed enrichment of lead, arsenic and nickel during post-monsoon, which were collected near the dumpsite due to the leaching of toxic elements from the dump site to the lakes. Some of the toxic elements like nickel and copper have not shown any dilution but have increased after the rains, which could be due to the leaching of arsenic from the dumpsite to the lake along with rainwater. Geochemical maps showing the distribution of heavy/trace elements in streams and lakes are prepared and presented in this paper. Effect of toxic elements on the health of the residents in the surrounding residential areas is also discussed.     

Perylene dominance in sediments from a subtropical high mountain lake

Perylene formation in sediments of water bodies has been a topic of continual discussion and debate. We report the concentration and age (ca. 660 yr) profiles of perylene and other polycyclic aromatic hydrocarbons (PAHs) in a sediment core from Emerald Peak Lake, the largest high mountain lake in Taiwan. Perylene is dominant at all depths of the sediment (ranging from 60% to 98% of total PAHs), a feature not commonly found in other sediments. The concentration profile of perylene with sediment age fits a first order kinetic model, which might be an indication of a steady sedimentary environment.     

浅水湖泊沉积物中磷的地球化学特征

对太湖不同污染状况和生态系统状况的湖区沉积物中磷的地球化学形态及其分布进行了研究。结果发现,沉积物的理化性质和磷的化学形态一般都在表层下深5～15cm发生明显的转折;草型湖区、藻型湖区、开阔湖面的大湖区沉积物的理化性质、间隙水中的磷浓度及沉积物中磷的形态存在较大的差异。东太湖沉积物间隙水磷浓度和交换态磷含量都显著低于其他湖区;风浪扰动相对剧烈的开阔湖面湖区沉积物中磷的沉积规律也不同于梅梁湾藻型湖区和东太湖草型湖区。研究表明,浅水湖泊中水生生物状况、风浪扰动状况对沉积物中磷的地球化学行为有至关重要的影响。     

Field scale heterogeneity of redox conditions in till-upscaling to a catchment nitrate model

Point scale studies in different settings of glacial geology show a large local variation of redox conditions. There is a need to develop an upscaling methodology for catchment scale models. This paper describes a study of field-scale heterogeneity of redox-interfaces in a till aquitard within an area of 600?×?600 m. The results showed significant variation of the depths to the redox-interface and thickness of the aquitard. Nitrate was present above the redox-interface but reduced to non-detectable levels a few metres below the interface. An upscaling approach for an area of 92 km² is proposed. Two models are proposed to predict the depth to the redox-interface in the aquitard and the resulting nitrate recharge concentrations to an underlying aquifer. The first model assumes that the depth to the redox-interface reflects the hydraulic head in the aquitard, and the second model assumes that the depth of the redox-interface is randomly distributed according to a log-normal probability distribution function. The upscaling approach using the random redox model estimated recharge concentrations comparable to the observed concentration in the underlying aquifer. The presented upscaling approach is applicable in distributed catchment models where sub-grid variability cannot be represented by the large grids.     

Bacteriohopanepolyols in tropical soils and sediments from the Congo River catchment area

The Congo River basin drains the second largest area of tropical rainforest in the world, including a large proportion of pristine wetlands. We present the bacteriohopanepolyol (BHP) inventory of a suite of tropical soils and, from comparison with published data, propose some initial ideas on BHP distribution controls. Strong taxonomic controls on BHP production are evident in wetland sediments. Dominant within the suite were 35-aminobacteriohopane-31,32,33,34-tetrol (aminotetrol) and 35-aminobacteriohopane-30,31,32,33,34-pentol (aminopentol), indicating aerobic methanotrophy. A narrow range and low mean relative abundance of 30-(5′-adenosyl)hopane (adenosylhopane) and related compounds, collectively termed “soil marker” BHPs, were observed in Congo soils (mean 17%, range 7.9–36% of total BHPs, n = 22) compared with literature data from temperate surface soils and Arctic surface soils (mean 36%, range 0–66% of total BHPs, n = 28) suggesting a greater rate of conversion of these BHP precursors to other structures.     

Seasonal succession and microlamina formation in a meromictic lake displaying varved sediments

In a small meromictic lake near Toronto, Canada, a mass mortality of photosynthetic bacteria followed the ventilation of the chemocline during fall (autumn) and resulted in 3–8 g m^-2 day^-1 of organic matter being deposited as a dark layer in sediment traps which were suspended in the permanently anaerobic zone. This mass mortality of photosynthetic bacteria occurred in late autumn following the annual thermal destratification of the lake's mixolimnion. Wind mixing during this period of homeothermy resulted in the introduction of low levels of dissolved oxygen into the lake's chemocline. The ensuing mass mortality of photosynthetic bacteria resulted in the release of elemental sulphur as the sulphur-rich bacteria decomposed and sank to the bottom of the lake. The ferrous ions in the water below a depth of 15 m in Crawford Lake reacted with this sulphur to form black ferrous sulphides and pyrite which formed a dark microlamina on the lake floor. Each dark microlamina was overlain by a light coloured (calcite-rich) layer which was deposited each spring and summer during the 3 yr period of this study. The mechanism of microlamina formation elucidated here has been based on the examination of bi-weekly sediment trap information. This approach has permitted an explanation of the mechanisms by which specific events such as calcite precipitation and phytoplankton seasonal succession are transcribed into the sediment record.     

Selective extraction of organically bound gold in soils, lake sediments and stream sediments

The extraction of organically bound gold from surficial materials is accomplished by using a solution of 5% sodium hypochlorite. A 10-g sample is digested at least twice with 50 mL of hypochlorite solution. The recovery of gold from the organic phase is nearly quantitative for lake sediments and stream sediments high in organic content. For stream sediments and soils low in organics, the recovery of gold is complicated by the sorption of released gold onto inorganic sample components. For these materials, recoveries as low as 70% of the organically bound gold are possible. For a stream sediment sample containing 53.4 ppb gold, the precision of the method is approximately 6% for a 10-g sample and 14% when a 5-g sample of stream sediment is used. The results obtained for all materials tested indicate that a substantial fraction of the gold found in sediments and soils exists as organically bound gold.     

Mobilization of gold into lake sediments from acid and alkaline mineralized environments in the southern Canadian Shield: Gold in lake sediments and natural waters

To be an effective indicator of mineralization in lake sediment surveys within the Canadian Shield, it is desirable that an element migrate in solution or adsorbed on suspensates. Given the low relief and disorganized drainage patterns of this region, dispersal in clastic form in drainage systems is limited and gives rise to erratic distributions. The purpose of this study was to discover whether Au shows significant hydromorphic mobility, which would justify the increasing use that is being made of this element in lake sediments as an indicator for gold mineralization.Waters and lake sediments were collected from Napier Lake, Ontario; PAP Lake, Saskatchewan; and Foster Lake, Manitoba, all of which contain Au-quartz vein mineralization and lie within the glaciated boreal forest zone of the Canadian Shield. In all three areas, profundal lake sediments down-drainage of mineralization contain Au concentrations higher than regional mean concentrations. Significant dissolution and transport of Au was found under oxidizing conditions associated with waters with pH that varied from acid to alkaline. Waters from drill holes penetrating mineralization contain up to 401 ng L⁻¹ Au (note; 1 ng L⁻¹ is equivalent to 1 part per trillion, 10⁻¹²). Surface waters overlying or near mineralization collected from bogs, seeps, ponds and streams contain up to 13 ng L⁻¹. The content of Au in lake waters is lower, with a maximum of 1.1 ng L⁻¹. There is also a detectable quantity of Au present in suspensates. Two samples of particulates (> 1 μm) filtered from lake water have Au equivalent to 0.17 ng L⁻¹ and 0.039 ng L⁻¹. While the contents of Au present in solution or as suspensates in lake and stream water are relatively small, they are sufficient, if precipitated, to generate anomalies in lake sediments. Thus for Reservoir Lake, in the Foster Lake area, water from the principal stream entering the lake carries 0.3 ng L⁻¹ Au. This provides an annual flux which far exceeds that required to generate the 7.3 ppb Au contained in profundal sediments of this lake; a content that is anomalous relative to the regional median content of < 1 ppb Au for lake sediments.Hydrogeochemical prospecting involving analysis for Au is one method for tracing the source of anomalous Au in lake sediments. Collection of 1 L samples without field treatment, followed by extraction of Au into MIBK, then analysis by graphite-furnace atomic absorption spectrophotometry, permits detection levels for Au of 0.5 ng L⁻¹. This is below the contents of Au found in some waters from mineralized areas. A detection limit of 0.3 ng L⁻¹ was obtained using larger water samples.     

Geochemistry of stream water in a catchment in Finland affected by sulphidic fine sediments

The impact of sediment type on stream water geochemistry was studied in a catchment in Finland affected by sulphidic fine-grained sediments. Stream water samples for general characterisation of water quality (pH, electrical conductivity) were taken at the basin outlet during various hydrological conditions, while samples for detailed geochemical analysis were collected at 119 sites in the catchment on one single occasion during high-water flow in autumn. The occurrence of sulphidic fine sediments was estimated based on data from an airborne electromagnetic survey carried out by the Geological Survey of Finland.Growing-symbol maps, which were prepared for each of the studied variables in water, and statistical calculations including factor analysis and Spearman correlations show that the concentrations of Al, Ga, U and Tl, all the lanthanides and several alkali and alkaline earth metals (K, Mg, Na, Li, Ca, Rb, Sr), transition metals (Cd, Co, Cu, Zn, Sc, Mn, Ni, Y, Hf) and non-metals (S, Br, I, Si) increase in water when the proportion of the catchment cover of sulphidic fine sediments increases. It is therefore argued that these elements are released and mobilised in considerable amounts by the oxidation and subsequent acidification and weathering of this type of sediment. Other elements are either slightly depleted in streams in areas of sulphidic fine sediments (V, Nb, Pb, Zr), have a distribution unrelated to sediment type (Fe, Cr, Cs, Mo), or are only weakly impacted by the occurrence of sulphidic sediments in the catchment (As, Ti, Ba). It is argued that these elements are not leached extensively from the oxidising sulphidic sediments, and that their distributions at least partly may be controlled by the contents of dissolved humic material and/or suspended organic and inorganic phases in the water.     

Tephra layers from Holocene lake sediments of the Sulmona Basin, central Italy: implications for volcanic activity in Peninsular Italy and tephrostratigraphy in the central Mediterranean area

We present a new tephrostratigraphic record from the Holocene lake sediments of the Sulmona basin, central Italy. The Holocene succession is represented by whitish calcareous mud that is divided into two units, SUL2 (ca 32 m thick) and SUL1 (ca 8 m thick), for a total thickness of ca 40 m. These units correspond to the youngest two out of six sedimentary cycles recognised in the Sulmona basin that are related to the lake sedimentation since the Middle Pleistocene. Height concordant U series age determinations and additional chronological data constrain the whole Holocene succession to between ca 8000 and 1000 yrs BP. This includes a sedimentary hiatus that separates the SUL2 and SUL1 units, which is roughly dated between <2800 and ca 2000 yrs BP. A total of 31 and 6 tephra layers were identified within the SUL2 and SUL1 units, respectively. However, only 28 tephra layers yielded fresh micro-pumices or glass shards suitable for chemical analyses using a microprobe wavelength dispersive spectrometer. Chronological and compositional constraints suggest that 27 ash layers probably derive from the Mt. Somma-Vesuvius Holocene volcanic activity, and one to the Ischia Island eruption of the Cannavale tephra (2920 ± 450 cal yrs BP). The 27 ash layers compatible with Mt. Somma-Vesuvius activity are clustered in three different time intervals: from ca 2000 to >1000; from 3600 to 3100; and from 7600 to 4700 yrs BP. The first, youngest cluster, comprises six layers and correlates with the intense explosive activity of Mt. Somma-Vesuvius that occurred after the prominent AD 79 Pompeii eruption, but only the near-Plinian event of AD 472 has been tentatively recognised. The intermediate cluster (3600–3100 yrs BP) starts with tephra that chemically and chronologically matches the products from the “Pomici di Avellino” eruption (ca 3800 ± 200 yrs BP). This is followed by eight further layers, where the glasses exhibit chemical features that are similar in composition to the products from the so-called “Protohistoric” or AP eruptions; however, only the distal equivalents of three AP events (AP3, AP4 and AP6) are tentatively designated. Finally, the early cluster (7600–4700 yrs BP) comprises 12 layers that contain evidence of a surprising, previously unrecognised, activity of the Mt. Somma-Vesuvius volcano during its supposed period of quiescence, between the major Plinian “Pomici di Mercato” (ca 9000 yrs BP) and “Pomici di Avellino” eruptions. Alternatively, since at present there is no evidence of a similar significant activity in the proximal area of this well-known volcano, a hitherto unknown origin of these tephras cannot be role out. The results of the present study provide new data that enrich our previous knowledge of the Holocene tephrostratigraphy and tephrochronology in central Italy, and a new model for the recent explosive activity of the Peninsular Italy volcanoes and the dispersal of the related pyroclastic deposits.