Previous paleolimnological studies demonstrated that the sediments of Garba Guracha, situated at 3950 m asl in the afro-alpine zone of the Bale Mountains of Ethiopia, provide a complete Late Glacial and Holocene paleoclimate and environmental archive. We revisited Garba Guracha in order to retrieve new sediment cores and to apply new environmental proxies, e.g. charcoal, diatoms, biomarkers, and stable isotopes. Our chronology is established using 210Pb dating and radiocarbon dating of bulk sedimentary organic matter, bulk n-alkanes, and charcoal. Although bedrock was not reached during coring, basal ages confirm that sedimentation started at the earliest ~ 16 cal kyr BP. The absence of a systematic age offset for the n-alkanes suggests that “pre-aging” is not a prominent issue in this lake, which is characterised by a very small afro-alpine catchment. X-ray fluorescence scans and total organic carbon contents show a prominent transition from minerogenic to organic-rich sediments around 11 cal kyr BP coinciding with the Holocene onset. While an unambiguous terrestrial versus aquatic source identification seems challenging, the n-alkane-based Paq proxy, TOC/N ratios, δ13C values, and the sugar biomarker patterns suggest a predominantly autochthonous organic matter source. Supraregional climate events, such as the African Humid Period, the Younger Dryas (YD), a 6.5 cal kyr BP short drying event, and the 4.2 cal kyr BP transition to overall drier climate are recorded in our archive. The Garba Guracha record suggests that northern hemisphere forcings played a role in the Eastern African highland paleoclimate.
Eastern Africa, and Ethiopia in particular, has received much attention from archeologists and paleoclimatologists (Viehberg et al. 2018; Lamb et al. 2018). This may be attributed to Quaternary climatic changes being widely acknowledged to have played a role in the early history of modern humans in Africa. Climatic extremes may have caused human populations to take refuge in the Ethiopian highlands (Brandt et al. 2012), including the Bale Mountains (Fig. 1). Ossendorf et al. (2019) recently highlighted that Middle Stone Age foragers occupied a rock shelter at 3469 m asl from 47 to 31 kyr BP, during times of the largest extent of the glaciation in the Bale Mountains.
Earlier studies of the Quaternary climate and environmental history of the Bale Mountains include Osmaston et al. (2005) on glacial geology, Kuzmicheva et al. (2017) on pollen and hyrax deposits and Gil-Romera et al. (2019) on pollen and charcoal. Umer et al. (2007) and Tiercelin et al. (2008) studied the sedimentary record of Garba Guracha, using sedimentological, geochemical and pollen analyses, showing that Garba Guracha is one of the longest, most continuous high-resolution Late Quaternary environmental archives from highland Africa.
Recently, the importance of compound-specific 14C dating in lake sediments has been shown by Douglas et al. (2014) and Gierga et al. (2016). The occurrence or nonoccurrence of age differences between organic matter components provides valuable information for the catchment itself and for the interpretation of proxies, especially in a multi-proxy approach.
The rationale for revisiting Garba Guracha was (1) to make this archive accessible by retrieving new sediment cores, (2) to examine age offsets in the organic matter components by applying bulk n-alkane dating and (3) to apply charcoal, diatom, biomarker and stable isotope analyses, not made in previous studies of the Garba Guracha cores. Together with non-pollen palynomorph and renewed pollen analyses, these new analyses provide proxy records of paleofire, limnology, vegetation, climate, and human environments. In this paper, we describe the sedimentary sequence and evaluate the organic matter origin of the new (2017) cores, establish a robust chronology with the first tephra correlations and present the first biogeochemical and biomarker results.
Garba Guracha is located in the Bale Mountains of the Bale–Arsi Massif, situated east of the Main Ethiopian Rift (Fig. 1). The highest plateau of the Bale Mountains is the Sanetti Plateau at an altitude between ~ 3800 to ~ 4200 m asl and an area of 600 km2 bordered by a steep escarpment to the south (Osmaston et al. 2005). The north and northeast are characterized by valley structures deeply incised by northward descending rivers. The volcanic plateau overlies older volcanic material and was formed by solidified horizontal lava consisting of alkali basalt, trachyte, and tuffs with rhyolites (Uhlig and Uhlig 1991; Williams 2016). The plateau and the valleys were locally glaciated during the Last Glacial Maximum (LGM) (Osmaston et al. 2005; Ossendorf et al. 2019). The glacial cirque Garba Guracha (6.875781 N, 39.878075 E) was first described by Werdecker (1962) and has also been described in detail by Umer et al. (2007) and Tiercelin et al. (2008). It is located at 3950 m asl, extends to about 500 × 300 m in size, has a maximum water depth of 6 m and a very small watershed (0.15 km2). The bedrock of the Garba Guracha catchment consists mainly of basaltic lavas. The cirque base is formed by trachytic tuff, which outcrops only on the southern and southeastern slopes (Tiercelin et al. 2008). The catchment bedrock is carbonate-poor (Löffler 1978; Uhlig and Uhlig 1991). The northeast-facing cirque lies between the Ericaceous and afro-alpine vegetation belts which are continuous on the northeastern side into the Togona Valley. The lake has an outlet during the rainy season. A marshy alluvial plain fed by several springs extends to the south of the lake.
The mean annual temperature at Dinsho (7.105016°N 39.776001°E, 3207 m asl, 25 km NNW of Garba Guracha) is 11.8 °C, and the mean minimum temperature for the coldest month is 0.6 °C (Hillman 1986). Ten newly installed climate stations across the Bale Mountains have provided modern climate data since 2017. The results from 2017 show a mean annual temperature of 4.9 °C at the Angesso Station (6.8964°N, 39.9085°E, 3949 m asl) which is located 4 km northeast of Garba Guracha.
Uhlig (1988) and Miehe and Miehe (1994) state that two moisture sources, the Indian Ocean monsoon and the equatorial westerlies, bring precipitation to the Bale Mountains. High seasonality characterizes the rainfall pattern with a dry season from November to February and a bimodal wet season from March to October. Precipitation maxima occur in April/May and September/October, respectively (Woldu et al. 1989). The highest monthly rainfall, related to the convergence of southwest and northeast air masses, occurs in the months of July to September. Mean annual precipitation increases with altitude from 925 mm at Goba (elevation 2720 m) to Chorchora with 1086 mm at 3500 m asl. At higher elevations, the mean annual precipitation decreases again (852 mm at Konteh, 4050 m) (Umer et al. 2007). Recently installed climate stations support this finding with annual precipitation in the year 2017 decreasing from 1097 mm at Angesso Station (elevation 3949 m) to 711 mm at the EWCP Station (elevation 4124 m) and even further to 468 mm at Tulu Dimtu (elevation 4385 m) (2017, unpublished data). The afro-alpine regions, including the Sanetti Plateau, are characterized by strong diurnal temperature differences between day and night. Hillman (1988) reported on a diurnal temperature range of 40 °C (− 15 °C to + 26 °C).
Material and methods
In February 2017, we retrieved two overlapping sediment cores using a Livingstone piston corer from a raft anchored at 4.8 m water depth. The replicate cores (BAL-GGU17-1A and BAL-GGU17-1B) were taken in sequential 1-m sections, with core 1B sections taken to overlap those of core 1A by 70 cm. Sediments at and below the water–sediment interface [Section BAL-GGU17-1A-1L (65 cm)] were sub-sampled at 1 cm intervals in the field. A maximum sediment depth of 1550 cm was reached, similar to the depth (1582 cm) achieved by Tiercelin et al. (2008). Unfortunately, that core was not available for further analyses. The bottom four sections of each of our cores were difficult to retrieve and extrude due to densely compacted sediments, coarse sand, and gravel. Bedrock or glacial diamicts were not reached. In the laboratory, the cores were split, described and stored at 4 °C. Sampling for chronological controls and proxy analyses was carried out on core BAL-GGU17-1B as its extrusion was more complete than core BAL-GGU17-1A.
Chronology and dating
For radiocarbon dating, we took a total of 31 samples, comprising 18 bulk sediment samples, 8 bulk n-alkane and 5 charcoal samples from the top 9 m of the BAL-GGU17-1B core (ESM1). Bulk n-Alkane and bulk sediment samples were taken at the same depths to test for age offsets.
Bulk sediment and charcoal samples were weighed into glass centrifuge vials and treated with 1 N HCl for 8 h at 60 °C to remove carbonates from the samples. They were subsequently washed and rinsed with ultrapure water to pH neutrality. Samples were then packed in tin boats (Elementar, 6 × 6 × 12) for 14C measurements.
For bulk n-alkane dating the total lipid extract (TLE) was obtained by constant rinsing with solvent (dichloromethane: methanol in a ratio of 9:1) using a soxhlet system. After rotary evaporation, the TLE was dissolved again with n-hexane and transferred onto aminopropyl pipette columns (Supelco, 45 um). The different fractions of the TLE (nonpolar fraction, including n-alkanes; polar fraction, including alcohols; acids) were selectively eluted from the columns using three solvents of increasing polarity (n-hexane; dichloromethane:methanol 1:1; diethyl ether:acetic acid 19:1). The n-alkane fraction was then loaded onto AgNO3-coated silica and zeolite pipette columns (Geokleen 5A, GHGeochemical Services) for further purification. The zeolite with the trapped n-alkanes was dried in an oven (12 h, 40 °C). After dissolving the zeolite in hydrofluoric acid, the n-alkanes were recovered using liquid–liquid extraction with n-hexane. Prior to 14C-measurements, the n-alkanes were transferred with dichloromethane (DCM) into tin capsules (Elementar, Art. Nr. 05001727, 3.5 × 5.5 × 0.1 mm) and the DCM was subsequently evaporated using a heating plate at 40 °C.
14C measurements were performed at the MIni CArbon DAting System (MICADAS) AMS coupled online to an elemental analyzer (Vario MICRO cube from Elementar) at the LARA AMS Laboratory, University of Bern (Szidat et al. 2014). Results were reported as fraction modern (F14C), which is the activity ratio of a sample normalized to the modern reference material Oxalic Acid II (National Institute of Standards and Technology). F14C results were corrected for cross and constant contamination following the contamination drift model of Salazar et al. (2015). Constant contamination for the bulk n-alkanes was obtained from 10 combined tin capsules that yielded 0.94 μg carbon for a single cap with F14C values of 0.8145. Constant contamination for the bulk sediment and charcoal samples was obtained from 10 combined tin boats that yield 1.41 μg carbon for a single boat with F14C values of 0.7390. 14C ages were calibrated to cal yr BP with the IntCal13 calibration curve (Reimer et al. 2013).
The dried sediment samples of the surface core BAL-GGU17-1A-1L were analyzed for 210Pb, 226Ra, 137Cs, and 241Am by direct gamma assay in the Environmental Radiometric Facility at University College London using an ORTEC HPGe GWL series well-type coaxial low background intrinsic germanium detector. Lead-210 was determined via its gamma emissions at 46.5 keV and 226Ra by the 295 keV and 352 keV gamma rays emitted by its daughter isotope 214Pb following 3 weeks storage in sealed containers to allow radioactive equilibration. Cesium-137 and 241Am were measured by their emissions at 662 keV and 59.5 keV (Appleby et al. 1986). The absolute efficiencies of the detector were determined using calibrated sources and sediment samples of known activity. Corrections were made for the effect of self-absorption of low energy gamma rays within the sample (Appleby et al. 1992).
Lead-210 dates were calculated using the CRS (constant rate of 210Pb supply) dating model (Appleby 2001). The CRS dating model places 1963 depth at 14.5 cm, which is considerably deeper than the depth suggested by the 137Cs and 241Am records. The corrected CRS chronologies and sediment accumulation rates were calculated by using the sediments at 7.5 cm as formed in 1963 (ESM1).
Spheroidal carbonaceous particle (SCP) analysis
Spheroidal carbonaceous particles (SCPs) are a component of fly-ash produced only from the high temperature industrial combustion of coal-series and oil fuels. SCP concentration profiles provide an additional means to provide independent dates at the regional scale while the rapid increase in SCP accumulation in the 1950s appears to be a global signal (Rose 2015). SCP analysis involved sequential removal of unwanted sediment fractions using nitric, hydrofluoric and hydrochloric acids resulting in a final suspension in water (Rose 1994). A known fraction of this suspension was then evaporated onto a coverslip, mounted onto a glass slide, and the SCPs enumerated under a light microscope at 400 × magnification. Standard criteria for SCP identification were followed (Rose 2008). Analytical blanks and SCP reference material (Rose 2008) were included with all sample digestions. The detection limit for the technique is typically less than 100 g DM−1 and calculated concentrations generally have an accuracy of approximately ± 45 g DM−1.
Three tephra layers (GGT-1, GGT-2, and GGT-3) were identified in the Garba Guracha sediments. These were geochemically fingerprinted to test whether they could be matched to the tephra layers that Martin-Jones et al. (2017) observed and dated in sediment cores from the Main Ethiopian Rift lakes, Tilo, Awassa, and Chamo. The oldest tephra layer GGT-3 has yet to be analyzed but may provide a further tie point to regional lakes in the future.
Samples were collected from across the entire thickness of the tephra and, in order to isolate glass shards for geochemical analysis, the samples were wet sieved to > 25 µm and separated using a solution of sodium polytungstate to a density of > 1.95 g cm−3. Shards from each tephra were mounted in an epoxy resin block which was ground and polished to reveal the interior of the glass for analysis. First, the shards were analyzed for major element concentrations using a Cameca SX-100 WDS electron microprobe (EPMA) at the Department of Earth Sciences, University of Cambridge. The analysis was set up to minimize alkali element migration through using a 10 µm defocused beam set at 6 nA and 15 kV and counting Na for 10 s, Cl and P for 60 s and all other elements for 30 s. A series of mineral standards were used to calibrate the instrument and concentrations were quantified using the PAP absorption correction method. Data presented in the text and figures have been normalized to 100% to account for variable secondary hydration of the glass; for the unprocessed data see ESM1.
Second, the glass shards were analyzed for their trace element concentrations using a Thermo Scientific iCapQ coupled to a Teledyne G2 Excimer laser (LA-ICP-MS) in the iCRAG laboratory, Trinity College Dublin. The shards were analyzed with 40 µm2 laser spots, with the laser firing at 5 Hz and counting for 40 s on both the sample and the blank. Counts were calibrated against assays of NIST612 with the average 29Si concentration for each tephra layer (obtained via EPMA) used as an internal standard. Data were reduced using Iolite3.4, using Ca correction as advocated by Tomlinson et al. (2010).
For each analytical session with the EPMA and the LA-ICP-MS, the MPI-DING basaltic, andesitic and rhyolitic natural glass standards (Jochum et al. 2006) were analyzed in order to monitor instrument accuracy.
For establishing an age-depth model, we used the Bayesian approach implemented in the package Bacon v 2.2 (Blaauw and Christen 2011) available for R (CRAN 2017). Bacon calibrates all 14C dates simultaneously according to the stratigraphic principle (Blaauw et al. 2007) applying the IntCal13 calibration curve (Reimer et al. 2013). This Bayesian method defines accumulation rates using a gamma autoregressive semi-parametric model with several subdivisions along the sediment that can be set up as a prior to the model (parameter α and thick respectively). This serves as a smoothness factor for the aging series, followed by a self-adjusting Markov Chain Monte Carlo (MCMC) building a robust-to-outliers age model (Blaauw and Christen 2011). The Bayesian approach aims to build a realistic age-depth relationship that often implies no linear deposition.
XRF analysis for both cores was performed at Aberystwyth University using the Itrax™ core scanner. Standard scanning procedure for an Itrax scanner was undertaken (Itrax scanner specifications and procedures outlined in (Croudace et al. 2006)). Scan settings were 30 kV, 45 mA using a step size of 500 μm for the Garba Guracha cores. XRF and X-ray exposure times were set to 15 s and 200 ms, respectively, for both cores. Fine-tuning of the detector parameters was performed before each scan to match the actual and fitted spectra and minimize the mean square error (MSE) value. As a result, MSE values were maintained below 2 (mean = 1.59 ± 0.3). Following the calibration of scanner settings, a layer of 1.5 μm thick film was used to cover the core to minimize moisture loss during scanning.
Significant changes in water and organic content may lead to inaccurate detection of some elements, resulting in downcore changes in raw element profiles unrelated to sediment geochemistry (Löwemark et al. 2011). Consequently, to minimize the effects of sediment–water and organic content, normalization of raw element data by the total scatter (both the incoherent and coherent data, equivalent to Compton and Rayleigh scattering, respectively) is commonly used (Kylander et al. 2011). Normalization of the peak area data was achieved using the total scatter.
Due to low and noisy signals, only K, Ca, Ti, Fe, and Rb could be evaluated robustly and were further considered for interpretation. The surface core (BAL-GGU17-1A-1L), as well as two core sections of BAL-GGU17-AB and 1B from 1245 to 1485 cm sediment depth, were not scanned because of high water content and coarse and gravel material, respectively. Therefore, the results presented in this study are missing the top 20 cm and 240 cm near the core base.
Total carbon (TC), total nitrogen (N) and stable carbon and nitrogen isotopic composition (δ13C and δ15N, respectively) were determined for 110 mixed sediment samples covering roughly 10 cm intervals. The analyses were carried out on dried and ground samples at the Institute of Agronomy and Nutritional Sciences, Soil Biogeochemistry, Martin-Luther-University Halle-Wittenberg using an EuroVector EA 3000 elemental analyzer (Hekatech, Wegberg, Germany) coupled via a Conflow III Interface to a Delta V Advantage isotope ratio mass spectrometer (IRMS; both from Thermo Fisher Scientific, Bremen, Germany). The results were calibrated using standard materials with known total carbon, nitrogen, 13C and 15 N contents (IAEA N2, IAEA CH6, IAEA NO3, IAEA CH7, IAEA 305A, USGS 41). Following the international standard regulations (Coplen 2011; 13C: Vienna Pee Dee Belemnite, VPDB; 15N: atmospheric N2, Air) all isotope results are reported in the common δ-notation. Concerning total carbon please note that (1) the bedrock in the catchment is reported to be carbonate-poor/free and (2) we performed Scheibler analyses (Allison 1960) on several sediment test samples that yielded 0% inorganic carbon content. Given that moreover, our TC record is in excellent agreement with the TOC record of Tiercelin et al. (2008), we use the term TOC instead of TC from here on for our record.
n-Alkane and sugar quantification
The n-alkanes from the extracted TLEs were quantified using a GC-2010 series gas chromatograph coupled with a flame ionization detector (GC-FID; Shimadzu, Kyoto, Japan). For linear calibration a C8–C40 saturated n-alkane standard mixture (Supelco 49452-U) was repeatedly analyzed in each batch at different concentrations (10 μg ml−1, 50 μg ml−1 and 100 μg ml−1). All work was carried out at the Institute of Agronomy and Nutritional Sciences, Soil Biogeochemistry, Martin-Luther-University, Halle-Wittenberg.
Sugar biomarkers were extracted following the method described by Zech and Glaser (2009). Briefly, the monosaccharides were hydrolytically extracted from the homogenized samples using 4 M trifluoroacetic acid at 105 °C for 4 h (Amelung et al. 1996). The monosaccharides were then filtered over glass fiber filters, evaporated and further purified over XAD-7 and DOWEX 50WX8 columns. After freeze-drying, the samples were derivatized (methyloxime-trimethylsilyl-derivatisation). The derivatization follows the method of Andrews (1989) to enable a quantification of a large range of sugars (arabinose (ara), fucose (fuc), galactose, glucose, mannose, rhamnose, ribose and xylose (xyl)). The quantification of these sugars was also carried out on a GC-FID (Shimadzu, Kyoto, Japan). Note that for this study only the sugar results for ara, fuc, and xyl are evaluated.
The sedimentary sequence—Master core and lithofacies
A master core of the overlapping BAL-GGU17-1A and 1B cores (Fig. 2) was created by visual correlation of several XRF elements like Ti, Fe, Rb, and K using Stratfit (Sagnotti and Caricchi 2018). Stratfit combines all core sections into one depth model. Additionally, the core sections were checked for contaminated parts, especially at the top and the bottom of individual core sections. The master core consists mainly of sections of the BAL-GGU17-1B core due to less contamination or disturbance than in core 1A. Only in the lower part of the sequence, a few 1A core sections were used instead of 1B core sections (Fig. 2).
The sedimentary sequence of core GGU17 consists of green banded siliciclastic fine material interbedded with layers of coarser material and gravel in the lower part (Fig. 2). It can be divided into 4 lithostratigraphic units:
Unit 1 (1552–1476 cm) contains greenish banded siliciclastic coarse sand.
Unit 2 (1476 – 1276 cm) is comprised of two meters of highly coarse silt and gravel.
Unit 3 (1276–1476 cm) consists mostly of green banded siliciclastic material mostly coarse silt with amorphous organic matter (OM) intersected with one layer of fine silt between 1219–1166 cm and a layer of coarse sand at 1031–966 cm. The diatom content of this unit is about 10%.
Unit 4 (838–70 cm) consists of nearly 8 m of dark brown massive organic mud with varying diatom content. This unit is intersected by a small layer of green-greyish massive siliciclastic fine silt at 828 cm and two layers of organic poor, finer sediments at 496 cm and 505 cm.
Three tephra layers have been identified at 129 cm, 604 cm, and 1198 cm depth, respectively. A fourth tephra layer mentioned by Tiercelin et al. (2008) (~ 340 cm) was not detected.
Two grey tephra layers were analysed as part of this study. They occur at 129 cm and 604 cm depth in the Garba Gurache core (Fig. 2), are no more than 1 cm in thickness and contain clear, bubble wall and pumiceous glass shards. According to the Garba Gurache age model, tephra GGT-1 has a modeled age of 1.2–1.6 cal kyr BP and GGT-2 has an age of 7.8–8.1 cal kyr BP. Glass shards in both tephra layers have a similar rhyolitic composition (ESM1), however, GGT-1 can be distinguished from GGT-2 based on its higher Ba concentrations.
Lead-210 activity and SCP
Total 210Pb activity reaches equilibrium with supported 210Pb at a depth around 52 cm of the core. Unsupported 210Pb activities, calculated by subtracting 226Ra activity (as supported 210Pb) from total 210Pb activity, decline overall irregularly with depth (ESM1). The unsupported 210Pb activity profile shows two different sections: the top 19 cm section and the rest of the core. Within each individual section, unsupported 210Pb activities decline more or less exponentially with depth, suggesting a relatively uniform sedimentation rate within the sections. However, as the decline gradients in the two sections are different, sedimentation rates might have changed at around 19 cm depth.
The 137Cs activity versus depth (ESM1) shows a well-resolved peak at 7.5 cm. Such a 137Cs peak has been found in other records from Eastern Africa (Panizzo et al. 2008; Stoof-Leichsenring et al. 2011). It is almost certain that this peak was derived from the 1963 fallout maximum of the atmospheric testing of nuclear weapons. A 241Am activity at 7.5 cm suggests the fallout of nuclear weapon testing, although one single point is not sufficient for dating (ESM1).
SCP concentrations increase to above detection limit at 11.5 cm and increase rapidly to a peak of almost 1000 g−1 (per gram dry mass) at 4.5 cm. Outside Europe and North America, such a profile is common, with the initial increase representing 1950 ± 5 years (Rose 2015). This would place 1950 ± 5 at 12 cm depth, in good agreement with the 210Pb chronology.
The 7 bulk n-alkane and 14 bulk sediment samples yielded sufficient carbon amounts of up to 138 µg for 14C dating (ESM1). Except for one n-alkane sample (low carbon mass of 16 µg), the bulk n-alkane and the bulk sediment samples obtained from the same core centimeters yielded similar ages without any systematic age offset. Additionally, there is no age offset for the three charcoal 14C ages. Apart from macrocharcoal particles (> 150 microns particles), we found no other terrestrial macrofossils suitable for 14C dating.
Age-depth model and sedimentation rate
To develop an age-depth model (Fig. 3), we combined the 210Pb, bulk sediment, bulk n-alkane and charcoal radiocarbon ages into a Bayesian modeling framework (Blaauw 2010; Blaauw and Christen 2011). Note that a preliminary version of this age-model underlies the paleoenvironmental dataset published by Gil-Romera et al. (2019). All 14C ages with a carbon mass smaller than 19 µg were rejected and not used for our age-depth model. Additionally, two ages that are not in stratigraphic order and three bulk sediment 14C ages at the core top which have an age offset to the 210Pb dating were excluded but are displayed in Fig. 3. According to the dating results and the established age-depth model, sedimentation in Garba Guracha started at about 15.9 cal kyr BP.
The mean sedimentation rate (MSR) for our BAL-GGU17-AB core is 1.25 mm a−1 (Fig. 3). The highest average values of 2.90 mm a−1 are recorded between 1110–990 cm with maximum values of 5 mm a−1. A second maximum is present from 900 to 720 cm with a sedimentation rate of 1.27 mm a−1. In between these maxima, a marked sedimentation minimum with decreased rates by up to 75% characterizes the time period from 12.8 cal kyr BP to 11.3 cal kyr BP. From 720 cm on, the sedimentation rate decreases constantly until the present day with a mean sedimentation rate of 0.70 mm a−1.
Establishing a robust chronology/sedimentation rate for the uppermost decimetres of the core is challenging because the combination of the two chronological methods provides us with a significant change in sedimentation rate that is most likely unrepresentative of the true sedimentation process. But since the modeled age is coherent with the sedimentation pattern of previous sections, and there is no significant change in any other proxies, we assume the radiocarbon-Cs/Pb age-transition to be valid. Therefore, MSR for the topmost 65 cm is 5.4 mm a−1.
The XRF scanning of the elements Rb, K, Ti, Fe, Ca, and Zr yielded the highest values in the lower part of the core with a stepwise decrease at 1200 cm and 800 cm to relatively low amounts. (Fig. 2). All these elements have a very high correlation coefficient of r > 0.93. At 500 cm an increase of Ca, Ti and Fe are coincide with low TOC values. Two short peaks in Zr, Rb, K and Fe reflect the tephra layers at 604 cm and 129 cm, respectively.
Organic geochemistry and stable isotope results
TOC values for the Garba Guracha master core range from 0.3% to 21.4% (Fig. 4). Low TOC persists until 840 cm. Above that depth, TOC values increase constantly until 355 cm with maxima at 630 cm (19.2%) and 430 cm (21.4%) and a minimum at 500 cm of 8%. At 355 cm, TOC rapidly decreases to values < 10%.
The TOC/N ratios range from 2.8 to 14.9. The lowest values prevail from the bottom of the core until 840 cm. Until 355 cm, relatively high ratios of up to 15 occur with short minima at 700 and 500 cm (9.5 and 6.5 cal kyr BP). Maxima characterize the depth between 640 and 610 and 460 and 355 cm.
The δ13C values range between −22.7 and −13.9‰. A decline in δ13C to lowest values (−22‰), coincides with an increase in TOC and TOC/N at 840 cm, followed by generally increasing values until 420 cm with a strong decrease at 600 cm. A small overall decrease continues to 160 cm. This interval includes a strong maximum of −16.3‰ at 340 cm and a weaker one (−16.8‰) at 355 cm. An increase is visible from 160 cm to the top of the core.
The δ15N values range from 1.3 to 5.8‰. From the bottom of the core to around 55 cm values stay stable around 3–4‰. A decrease with a minimum (1.3‰) at 525 cm is followed by a maximum between 500 and 355 cm (4–5.8‰). Values decrease again until 170 cm.
Paq and sugar ratios
Using the quantification of n-alkanes and sugar biomarkers, different ratios can be calculated to distinguish between terrestrial versus aquatic sources. Calculated ratios in this study cover the first 940 cm of the core due to insufficient organic matter content in the lower parts.
A common ratio for n-alkanes to differentiate aquatic macrophyte input versus emergent and terrestrial vegetation input is the Paq proxy (Ficken et al. 2000), defined as
The Paq ratio values range between 0.04 and 0.57 (Fig. 5). Highest values are present between 940 and 780 cm (up to 0.57) with one minimum at 840 cm (0.33). A shift to lower values occurs with a minimum at 750 cm (0.22) and a maximum at 500 cm (0.41). Like the TOC and TOC/N values the Paq decreases drastically at 355 cm. Followed by a phase of low values until 260 cm. The last 260 cm have intermediate values with a minimum at 155 cm (0.04).
Hepp et al. (2016) developed two sugar biomarker ratios defined as fuc/(ara + xyl) and fuc/(ara + xyl).
The fuc/(ara + xyl) ratios range from 0.2 to 0.8 (Fig. 5). The highest values concur with the highest values of the Paq ratio from 940 to 780 cm with a maximum at 795 cm (0.5). A more abrupt shift to lower values occurs at 770 cm. Low values proceed until 260 cm with a maximum at 485 cm (0.6) and a minimum at 720 cm (0.3). After a maximum at 235 cm (0.5), the lowest values of the core prolong between 235 and 145 cm. The last 140 cm are characterized by a strong increase with a maximum at 85 cm (0.58).
The (fuc + xyl)/ara ratios range between 0.7 and 3 (Fig. 5). The ratio correlates well with the fuc/(ara + xyl) ratio for the top 235 cm with minima at 145 and 195 cm. The highest values are reached between 390 and 490 cm (up to 3). Low values at 690 to 740 cm correlate well with the fuc/(ara + xyl) ratio. However, underneath 770 cm when the fuc/(ara + xyl) ratio shows the highest values the (fuc + xyl)/ara ratio displays conditions with values between 1.3 and 1.9.
Rhyolitic tephras, of similar composition to the Gurba Gurache tephras, have also been documented in Holocene sediment cores from the Main Ethiopian Rift lakes Tilo and Chamo (Martin-Jones et al. 2017). Fourteen tephra layers were identified in the < 10 kyr Lake Tilo sequence by Martin-Jones et al. (2017), who geochemically correlated two of these horizons (TT-2 and TT-13) to two tephra layers occurring within sediments from Lake Chamo, 170 km to the south. Martin-Jones et al. (2017) suggested that the Corbetti caldera (~ 40 km east of Lake Tilo), which erupts tephras of a distinct composition in comparison to other Ethiopian Rift volcanoes, is the source of the tephras found at lakes Tilo and Chamo. Fontijn et al. (2018) later correlated TT-2 and TT-13 to their on-land equivalents in outcrops within the Corbetti caldera, confirming this as the source for these two eruptions.
To test if the Garba Guracha tephras were also deposited by eruptions from Corbetti (~ 120 km to the west of our site) we compared the glass composition of GGT-1 and GGT-2 with the Tilo and Chamo tephras (ESM1). Tephra GGT-1 matches the composition of the Tilo tephra TT-2, which is dated at Lake Tilo to 1.3–1.5 cal kyrs BP. Martin-Jones et al. (2017) geochemically correlated TT-2 to the youngest of the Chamo tephras CHT-1 (1.5–1.9 cal kyrs BP), and this deposit represents Corbetti’s most recent highly explosive eruption. Tephra GGT-2 has a similar composition to glass within the Tilo tephra TT-13 (dated at Tilo to 8.3–8.7 cal kyrs BP), which correlates to CHT-2 at Lake Chamo and where it is dated to 7.8–8.3 cal kyrs BP. GGT-1 and GGT-2 glass does, however, contain lower concentrations of Zr, Th, and Ba than the Tilo and Chamo tephra glass shards. These eruptions may have tapped a compositionally stratified magma chamber resulting in wide-ranging tephra compositions. Garba Guracha is the first distal site to the east of Corbetti for which we have glass data, and if wind direction changed mid-eruption this could explain why we have a slightly different tephra compositions deposited in this new location.
Although the Corbetti tephras are compositionally zoned, making their recognition in different locations more challenging, the existing evidence for the widespread dispersal of tephras TT-2 and TT-13 supports our tentative geochemical correlations to the distal tephra layers preserved at Garba Guracha. Here we use these tephra correlations as an external test of the Garba Guracha age model. Whilst the tephra layers recorded in lakes Tilo and Chamo have greater uncertainties than the Garba Guracha tephras, these horizons act as useful markers around which we can compare environmental indicators recorded in the different lakes. Our correlations to the well-dated Garba Guracha record allow us to refine the ages of these two highly explosive Holocene eruptions from the Corbetti caldera.
The 2017 Garba Guracha core covers the range from the present day to ~ 15.9 cal kyr BP. Tiercelin et al. (2008) suggested the minimum age of deglaciation to be ~ 16.7 cal kyr BP. Exposure dating (15 ± 1 cal kyr BP) of bolders and glacial features in the Togona Valley (down hill from Garba Guracha) support a later minimum age of deglaciation (Ossendorf et al. 2019; Groos unpublished data). The modeled ages for the two tephra layers at 129 and 604 cm are 1.2–1.6 and 7.8–8.1 cal kyr BP, respectively. These tephra ages compare well with the ages of their geochemical correlatives (Fig. 3). The independent chronological context provided by the tephra layers on the Garba Guracha age model not only underlines the robustness of the age model but also allows us to conclude that the offset between 14C bulk sediment and 210Pb ages in the top of the core (ESM1) is not a systematic age offset. Due to the fact that the 210Pb ages are supported by SCP and a hard water effect of the 14C ages can be ruled out, we hypothesize the input of pre-aged terrestrial organic matter after ~ 1 cal kyr BP.
An old carbon input could also explain the stratigraphically inconsistent older 14C bulk sediment ages at 794 and 821 cm. Interestingly an n-alkane date at 794 cm (9.7–11.2 cal kyr BP), which has been excluded due to low carbon mass suggests a younger age more in agreement with the current age-depth model (Fig. 3). Higher runoff after 11.3 cal kyr BP (i.e. after the YD period) might have led to an input of old terrestrial organic matter with low n-alkane content (less vegetation during the YD cold phase). Therefore, bulk sediment could be more strongly pre-aged than the n-alkane component.
In the literature, pre-aging effects have been described for bulk sediment (Sirocko et al. 2013) and n-alkanes (Douglas et al. 2014; Gierga et al. 2016) because terrestrial material/biomarkers can be stored in soils for a long period before being transported into the sediment (Raymond and Bauer 2001). In soils or sediments, n-alkanes can be preserved due to their chemical inertness, resistance against degradation and low water solubility (Eglinton and Eglinton 2008). If the catchment area does not yield old carbon pools and the residence times for biomarkers are short, bulk n-alkane dating that was previously undertaken by (Bliedtner et al. 2020; Häggi et al. 2014; Haas et al. 2017; Zech et al. 2017) is hence corroborated as a valuable tool for dating lacustrine sediments in addition to compound-specific n-alkane 14C dating (Gierga et al. 2016).
The small Garba Guracha catchment with poorly developed soils favors rapid sedimentation and n-alkane deposition without considerable pre-aging effects. A contribution of aeolian transported plant-waxes cannot be completely discounted, despite the negligible old carbon input. Yet, for most parts of the core, our 14C results suggest that (i) either the terrestrial n-alkanes have a very short residence time in the catchment (ii) and/or the n-alkanes are primarily of the same allochthonous/autochthonous origin as the bulk sedimentary organic matter.
Origin of organic matter
Distinguishing between allochthonous (terrestrial) versus autochthonous (aquatic) OM is a crucial issue in paleolimnological studies (Brenner et al. 1999; Meyers 2003). For instance, TOC/N ratios < 10 (Meyers 2003) are frequently used as indicators for primarily autochthonous-derived OM. By contrast, terrestrial higher plants (due to a higher amount of carbon-rich lignin and cellulose) are typically characterized by higher TOC/N ratios (> 20) (Meyers 1994). It should be acknowledged, however, that degradation and mineralization of terrestrial OM result in lower TOC/N ratios, as well as in more positive δ13C values (Zech et al. 2007). In a study by Mekonnen et al. (2019), it is shown that the leaves of Erica in the Bale Mountains have very high TOC/N ratios of about 55, whereas Ah horizons underneath Erica yielded TOC/N ratios of around 17. The TOC/N ratios of the Garba Guracha core reveal a wide range from 2.8 to 14.9 (Fig. 6). While a predominantly allochthonous OM input can be excluded, a partial terrestrial OM input cannot be ruled out for the Early to Mid-Holocene. At the same time, the planktonic microalgae Botryococcus braunii became more abundant during the Early and Mid-Holocene with a clear maximum from 6.5 to 4.2 cal kyr BP (Umer et al. 2007) (Fig. 6). B. braunii is known for unusually high TOC/N ratios compared to other algae (Leng and Marshall 2004). This is confirmed by a B. braunii sample that we cultivated and that yielded a TOC/N ratio of 18 and a δ13C value of -13.8 ‰. Higher TOC/N values due to a strong abundance of B. braunii may, therefore, be misinterpreted as an increase in allochthonous OM input.
According to Brenner et al. (2006) and O’Leary (1988), C3 vascular plants are characterized by δ13C values ranging between -25 ‰ and -35 ‰. By contrast, C4 plants are characterized by less negative δ13C values ranging between − 16 to −10 ‰ and algae can produce δ13C values up to − 12‰. Given that there is no evidence hitherto for the occurrence of C4 plants in our catchment (Mekonnen et al. 2019), the overall relatively positive δ13C values of Garba Guracha (≥ −22.7 ‰, Fig. 6) support a dominant autochthonous OM input.
Apart from bulk sedimentary OM, source identification can be done on a molecular level, too. Concerning n-alkane biomarkers, Ficken et al. (2000) introduced the Paq index based on the finding that submerged and floating aquatic plants from a lake on Mt. Kenya are characterized by values between 0.4 and 1, whereas terrestrial plants yielded values lower than 0.1. According to this proxy, aquatic-derived n-alkanes dominate the YD sediments, a mixture of aquatic- and terrestrial-derived n-alkanes dominate the Early and Mid-Holocene sediments and terrestrial-derived n-alkanes dominate at least partly the Late Holocene sediments (Fig. 6). However, we recommend caution when using the Paq proxy, because there is increasing evidence for potentially erroneous interpretations. While Hepp et al. (2018) emphasized the high production of the ‘aquatic’ n-alkane nC23 by birch rendering the Paq proxy invalid in European Late Glacial sedimentary archives, Baas et al. (2000) and Tarasov et al. (2013) report on high nC23 and nC25 concentrations of Sphagnum species, a fern and a sedge species. Moreover, the Paq interpretation for the Late Holocene part of Garba Guracha is clearly in contradiction with the TOC/N and δ13C interpretation (Fig. 6). At the current state of research, an unambiguous terrestrial versus aquatic source identification of the n-alkane record of Garba Guracha hence seems challenging.
Concerning the sugar biomarkers, Hepp et al. (2016) found terrestrial plants and mosses to be characterized by fuc/(ara + xyl) ratios < 0.1, whereas algae are characterized by ratios > 0.1. The results for Garba Guracha (Fig. 6) thus suggest a predominantly aquatic (algae) origin of the sugars. This finding can also be nicely illustrated in a ternary diagram (Fig. 5) and highlights that the interpretation of predominantly aquatic-derived sugars is in good agreement with the ‘aquatic’ TOC/N and δ13C interpretation.
Phase 1: (1548–995 cm; 16–12.8 cal kyr BP)
The highest values of the elements Rb, K, Ti, Fe, and Zr used to detect changes in minerogenic/lithogenic influx (Kylander et al. 2011), are likely representing relatively high minerogenic input attributable to glacial retreat in the catchment. In contrast to Tiercelin et al. (2008), we found no evidence for low sedimentation rates prevailing during the early Late Glacial; instead, we found high mean sedimentation rates of up to 1.86 mm a−1. This implies a fast filling glacial cirque, potentially fed by a melting glacier forced by rising temperatures. Sparse vegetation in the catchment (Umer et al. 2007; Gil-Romera et al. 2019) and low algal productivity in the meltwater-fed lake could have been a small OM source represented by low TOC values of up to 1%. Low TOC/N values of 5 and relatively positive δ13C values (−19 to 14 ‰) point to aquatic algae as the dominant OM source (Meyers 2003; Brenner et al. 2006).
At ~ 14 cal kyr BP an increasing mean sedimentation rate of up to 2.2 mm a−1 was dominated by detrital input as represented by high, but decreased, K, Rb, Ti, and Zr values which suggest continued, rapid in-filling of the lake fed by glacier retreat. Here our data and interpretation agrees with Tiercelin et al. (2008) in that the strong rise in sedimentation rate is due to stronger glacial recession probably caused by increasing temperatures and/or higher precipitation.
Phase 2: (995–900 cm, 12.8–11.2 cal kyr BP)
During this interval sedimentation rates decreased dramatically by nearly 75% to 0.60 mm a−1, indicating either a drier or colder climate. Cold conditions may have favored a longer season of ice-cover on the lake, whereas dry conditions would be associated with less runoff into the lake. In either scenario, we would expect to see not only a change in sedimentation but also a lower OM input into the lake. This is supported by low TOC values and decreased dominance of Erica heathlands, which, as revealed in the Garba Guracha pollen data, dominated the local vegetation during this phase (Umer et al. 2007; Gil-Romera et al. 2019). Additionally, aquatic production would likely have been reduced due to lower insolation during ice cover and lower input of nutrients.
This dry or/and cold period coincides with the YD in the Greenland ice cores (Alley 2000). The more precise timing of this phase of low sedimentation rate due to our robust and higher resolution chronology allows us to re-address previous discussions of the YD at Garba Guracha (Tiercelin et al. 2008). Younger Dryas-like conditions have been described in Eastern Africa before (Roberts et al. 1993; Talbot et al. 2007). Marshall et al. (2011) suggest likewise a phase of low sedimentation rate for Lake Tana during the YD due to reduced precipitation and runoff. During the YD, a weakening of the North Atlantic Deep Water formation, linked to increased freshwater input, is thought to have caused a sea surface temperature anomaly with reduced precipitation in the tropics and associated lake low stands (Street-Perrott and Perrott 1990). Climate modelling results (Chiang and Bitz 2005; Broccoli et al. 2006) support the idea of Nicholson (1982) that an interhemispheric thermal gradient forces the ITCZ south of the equator. A more recent modelling approach suggests a period of dry north winds during cold phases like Heinrich event 1 or YD (Mohtadi et al. 2014). Dry conditions coinciding with the YD have been reconstructed in several Eastern African lakes including Lake Victoria (Talbot and Lærdal 2000; Stager et al. 2002), Lake Suguta (Junginger et al. 2014), the Ziway–Shala basin (Gillespie et al. 1983), and Lake Albert (Beuning et al. 1997).
Phase 3: (900–340 cm, 11.2–4.5 cal kyr BP)
From the beginning of this phase until 10.8 cal kyr BP, the mean sedimentation rate more than doubled to 1.37 mm a−1. The reason for this may have been increasing temperatures due to higher insolation (Fig. 6) and increasing precipitation resulting in a stronger runoff. Both are supported by increasing TOC values and an higher hydrogen index (Tiercelin et al. 2008) pointing to more favorable conditions for aquatic and terrestrial OM production. Additionally, a change in OM production is recorded by an increasing TOC/N ratio from less than 5 to around 12. However, input of eroded old organic matter (formed during phase 2) cannot be ruled out.
After 10.8 cal kyr BP the sedimentation rate decreased slightly to 1.25 mm a−1 until 9.8 cal kyr BP and in a second step more strongly to 0.72 mm a−1. Additionally, lower Ti, Fe, Ca, K and Rb counts and a TOC increase up to 18% indicate less minerogenic input and higher organic matter production. This change may be indicative of the progression of the catchment from a glacier-dominated catchment without vegetation to a cirque lake catchment with soil development and vegetation cover.
A drop of TOC and TOC/N ratios coincides with the 8.2 kyr event in the northern hemisphere, known as a short cold spell (Dansgaard et al. 1993; Bond et al. 1997). For this most pronounced climate shift in the Holocene, a period of drought has been reconstructed for the Ziway–Shala system (Gillespie et al. 1983), Lake Malawi (Gasse et al. 2002), and Lake Tilo (Leng et al. 1999). Thompson et al. (2002) found a maximum in wind-blown fluoride derived from dry lake basins in the Kilimanjaro ice record at ~ 8.4 cal kyr BP.
A pronounced TOC minimum with a drop to 10% coinciding with a tephra layer at 7.9 cal kyr BP is followed by a phase of decreased TOC with a minimum of 8% at 6.5 cal kyr BP. At 6.5 cal kyr BP a small maximum of higher minerogenic input marked by higher Rb, Ti, Ca and K counts concur with two organic poor layers in the core. Additionally, Paq, fuc/(ara + xyl) and (fuc + xyl)/ara indicate a lower terrestrial OM input, which is supported by the reduced vegetation cover at that time in the lake’s catchment (Gil-Romera et al. 2019). These findings represent a drought period, which is in agreement with an arid period found in a speleothem record in southern Oman (Fleitmann et al. 2007).
Between 6 cal kyr BP and 4.5 cal kyr BP the highest OM production (TOC ~ 20%) of the core occurs. It coincides with the highest abundance of B. braunii (Umer et al. 2007), which could explain the highest TOC/N values of the entire core rather than an increased allochthounous OM input. A higher allochthounous OM input is contradicted by positive delta 13C values in this phase which accompany a B. braunii increase. Blooms of B. braunii are associated with phosphorus availability due to high inwash (Huang and Hong 1999). This could point to a phase of increased nutrient availability and stronger aquatic productivity.
Phase 4 (340–70 cm, 4.5–0.3 cal kyr BP)
Contemporaneous with a strong decrease of B. braunii (Umer et al. 2007), TOC and the TOC/N ratio drop massively to 7% and 8 respectively. Less favorable conditions for OM in the Garba Guracha record coincide with a known drought phase due to a weak monsoon in the Indian ocean records (Fleitmann and Matter 2009; Nakamura et al. 2016) and aridity in North Africa (Gasse 2000; Marchant and Hooghiemstra 2004).
The 4.5 kyr drought event is followed by a period of increased precipitation as evidenced by a slightly increased mean sedimentation rate to 0.85 mm a−1 for around 1000 years before it decreases to 0.66 mm a−1. TOC is around 15% with some variations and TOC/N decreases to 7–9. At 1.5 cal kyr BP minima in the Paq, δ13C and sugar ratios point to an increased terrestrial OM production followed by an increase in aquatic production until the Little Ice Age at ~ 0.6 cal kyr BP represented in the sugar biomarker ratios.
The high-altitude Garba Guracha archive reflects local and supraregional climate changes beginning with deglaciation at around 15.9 cal kyr BP pointing to a temperature increase as a consequence of rising insolation (Laskar et al. 2004). This temperature increase may have been even stronger compared to low land ecosystems (Loomis et al. 2017). Increasing temperatures and precipitation at the beginning of phase 3 led not only to favorable conditions for OM production after the YD (phase 2) but also to prolonged humid conditions (phase 3) due to an enhancement of East and West African monsoon intensity in contrast to the reduced monsoonal activity during the YD (Umer et al. 2007) and a change in atmospheric circulation (Tierney et al. 2011; Costa et al. 2014; Junginger et al. 2014). This coincides with the AHP (deMenocal et al. 2000) and rising lake levels in Eastern Africa (Gasse 2000; Junginger et al. 2014; Lezine et al. 2014). A shift to arid conditions at 4.5 kyr may mark a late termination of the AHP in the Garba Guracha record and may indicate a late response of a high-altitude aquatic system. However, Erica pollen already decreased at 5.2 kyr (Gil-Romera et al. 2019). A return to wetter conditions between 2.5 and 1.5 kyr concurs with rising lake levels in the Horn of Africa region (Lezine et al. 2014).
Comparison with lake level and other records
Garba Guracha appears to have reacted sensitively to local and supraregional climate changes. Despite favourable conditions for OM production are indicated by TOC and TOC/N, we should be careful when interpreting TOC and TOC/N as climate proxies because local factors may overprint supraregional climate change effects on these proxies. For example, a TOC decrease at 7.9 cal kyr BP coincides with a volcanic eruption (GGT-1 tephra), and TOC increases may be explained for instance by high algal production (Umer et al. 2007).
However, the inferred timing of favorable conditions in the Early to Mid-Holocene for OM production (TOC and TOC/N) shows similarities with a TOC record from Lake Turkana (Morrissey and Scholz 2014) and coincides with lake level fluctuations of Lake Turkana (Garcin et al. 2012; Bloszies et al. 2015; Beck et al. 2019), Lake Suguta (Junginger et al. 2014), Chew Bahir (Foerster et al. 2012), Lake Abhé (Gasse 2000), Lake Dendi (Wagner et al. 2018), and Lake Ziway-Shala (Gillespie et al. 1983). The offset shown in our record at the Holocene onset may be altitude-related as during deglaciation, high-altitude climate records might be buffered due to slow melting of the remaining ice in the catchment, especially given the northward aspect of Garba Guracha (Tiercelin et al. 2008). Several minima in our TOC and TOC/N record coincide with drought phases in other Eastern African and Oman records at 10.7 cal kyr BP (Junginger et al. 2014; Wagner et al. 2018), 8.2 cal kyr BP (Gasse 2000; Garcin et al. 2012; Costa et al. 2014; Junginger et al. 2014) and 6.5 cal kyr BP (Fleitmann et al. 2007). The decrease of TOC and TOC/N values at 4.5 cal kyr BP concurs better with the North-Ethiopian lake records (Lake Ziway-Shala (Gillespie et al. 1983) and Lake Abhé (Gasse 2000)) than with the South-Ethiopian lake records (Junginger et al. 2014).
Moreover, it has been shown that the timing of the AHP termination depends not only on the archive but on the investigated proxy (Castañeda et al. 2016). This holds true for the Garba Guracha archive with the decline of Erica pollen already beginning at 5.2 cal kyr BP (Gil-Romera et al. 2019), 700 years earlier than the TOC and TOC/N record. An AHP termination at 5.2 cal kyr BP would concur with South-Ethiopian lake records (Junginger et al. 2014).
The different response of lake records in Eastern Africa during the Holocene might be explained, despite local factors, by two possible mechanisms: (1) an increase of atmospheric moisture depending on the ITCZ shift and thus on insolation and (2) an eastward shift of the Congo Air Boundary due to an enhanced pressure gradient between India and Eastern Africa (Tierney et al. 2011; Costa et al. 2014; Junginger et al. 2014; Castañeda et al. 2016). Due to the blurring of local factors on TOC and TOC/N and the different timing of proxies in connection with the AHP termination, further research, and other proxies, especially water isotopes, may be needed to help disentangle the conflicting evidence.
Garba Guracha provides one of the best dated Late Glacial – Holocene continuous high-altitude records in Eastern Africa. It offers a relatively small, undisturbed catchment where global and local climate influences can be studied. New sedimentary data and a more detailed and robust chronology give new insights into the sedimentary history and the catchment dynamics of Garba Guracha.
The chronology of the Garba Guracha record spans the last ca. 16 cal kyr BP. Bulk sediment and bulk n-alkane dates are in good agreement with charcoal and tephra ages. n-Alkane ages show no age offset to 14C bulk sediment dating. We propose that a pre-aging effect for terrestrial n-alkanes or terrestrial material, in general, is negligible for most of the record due to short residence times for terrestrial material in the small catchment area and due to the high lake productivity. We conclude that our chronology is robust and that dating of bulk n-alkanes is a valuable tool for lake sediment dating in small catchment areas. The Garba Guracha sedimentary archive records the environmental change from deglaciation to a precipitation-fed lake. The record shows well-known climate changes such as the YD and the arid ~ 6.5 and ~ 4.2 kyr events. The occurrence of these events clearly shows regional and northern hemispheric influence on the high-altitude Eastern African ecosystems. Since the Holocene onset, organic-rich sediments point to climatic conditions favorable for aquatic biomass production due to higher temperatures and increased precipitation.
The high resolution environmental and chronological data presented in this study, alongside the uniqueness of the Garba Guracha site, allow us to pick out the complexity of past climates in the Ethiopian Rift and highlands. Our data suggest similarities between Garba Guracha and other sites in the region, but clearly there are temporal and spatial variations in how the past climate changes are manifested. Future publications and further study using a wider network of sites may enable us to understand leads and lags in the past climates of Eastern Africa in greater depth.
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Open Access funding provided by Projekt DEAL. This research was funded by the German Research Council (DFG) in the framework of the joint Ethio-European DFG Research Unit 2358 “The Mountain Exile Hypothesis. How humans benefited from and re-shaped African high-altitude ecosystems during Quaternary climate changes”. We thank the Ethiopian Wildlife Conservation Authority for permitting our research in the Bale Mountains National Park. We are grateful to the project coordination, the Philipps University Marburg, University of Addis Abeba, the Frankfurt Zoological Society, the Ethiopian Wolf Project, the Bale Mountains National Park, and the related staff members, especially Katinka Thielsen, Mekbib Fekadu, Bahru Zinaye Asegahegn, Elias Tadesse, Ermias Getachew, and Terefe Endale, for their logistic assistance during our fieldwork. CMJ was supported by the Geography Laboratories, Cambridge, and thanks Iris Buisman (Cambridge) and Emma Tomlinson (Trinity College, Dublin) for guidance with tephra analysis. We thank the team of the Soil Biogeochemistry Department at Martin Luther University Halle Saale for the support during lab work, in particular, Marianne Benesch and Heike Maennike.
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Bittner, L., Bliedtner, M., Grady, D. et al. Revisiting afro-alpine Lake Garba Guracha in the Bale Mountains of Ethiopia: rationale, chronology, geochemistry, and paleoenvironmental implications. J Paleolimnol 64, 293–314 (2020). https://doi.org/10.1007/s10933-020-00138-w
- Radiocarbon dating
- XRF scanning
- Sedimentation rate