Erosion and the Rejuvenation of Weathering-derived Nutrient Supply in an Old Tropical Landscape

Studies of long-term soil and ecosystem development on static geomorphic surfaces show that old soils become depleted in most rock-derived nutrients. As they are depleted, however, static surfaces also are dissected by fluvial erosion. This fluvial erosion leads to colluvial soil transport on the resulting slopes, which in turn can rejuvenate the supply of weathering-derived nutrients to plants. We evaluated the influence of erosion and consequent landscape evolution on nutrient availability along a slope on the Island of Kauai, near the oldest, most nutrient-depleted site on a substrate age gradient across the Hawaiian Islands. Noncrystalline minerals characteristic of younger Hawaiian soils increased from 3% of the soil on the static constructional surface at the top of the slope to 13% on the lower slope, and the fraction of soil phosphorus (P) that was occluded (and hence unavailable) decreased from 80% to 56% at midslope. Foliar nitrogen and P concentrations in Metrosideros polymorpha increased from 0.82% and 0.062% to 1.13% and 0.083% on the constructional surface and lower slope, respectively. The increase in foliar P over a horizontal difference of less than 250 m represents nearly half of the total variation in foliar P observed over 4.1 million years of soil and ecosystem development in Hawaii. The fraction of foliar strontium (Sr) derived from weathering of Hawaiian basalt was determined using ⁸⁷Sr:⁸⁶Sr; it increased from less than 6% on the constructional surface to 13% and 31% on lower slope and alluvial positions. Erosional processes increase both nutrient supply on this slope and the fine-scale biogeochemical diversity of this old tropical landscape; it could contribute to the relatively high level of species diversity observed on Kauai.     

Use of foliar Ca/Sr discrimination and <Superscript>87</Superscript>Sr/<Superscript>86</Superscript>Sr ratios to determine soil Ca sources to sugar maple foliage in a northern hardwood forest

Calcium/strontium and ⁸⁷Sr/⁸⁶Sr ratios in foliage can be used to determine the relative importance of different soil sources of Ca to vegetation, if the discrimination of Ca/Sr by the plant between nutrient sources and foliage is known. We compared these tracers in the foliage of sugar maple (Acer saccharum) to the exchange fraction and acid leaches of soil horizons at six study sites in the White Mountains of New Hampshire, USA. In a previous study, sugar maple was shown to discriminate for Ca compared to Sr in foliage formation by a factor of 1.14 ± 0.12. After accounting for the predicted 14% shift in Ca/Sr, foliar Ca/Sr and ⁸⁷Sr/⁸⁶Sr ratios closely match the values in the Oie horizon at each study site across a 3.6-fold variation in foliar Ca/Sr ratios. Newly weathered cations, for which the Ca/Sr and ⁸⁷Sr/⁸⁶Sr ratios are estimated from acid leaches of soils, can be ruled out as a major Ca source to current foliage. Within sites, the ⁸⁷Sr/⁸⁶Sr ratio of the soil exchange pool in the Oa horizon and in the 0–10 cm and 10–20 cm increments of the mineral soil are similar to the Oie horizon and sugar maple foliar values, suggesting a common source of Sr in all of the actively cycling pools, but providing no help in distinguishing among them as sources to foliage. The Ca/Sr ratio in the soil exchange pool, however, decreases significantly with depth, and based on this variation, the exchange pool below the forest floor can be excluded as a major Ca source to the current sugar maple foliage. This study confirms that internal recycling of Ca between litter, organic soil horizons and vegetation dominate annual uptake of Ca in northern hardwood ecosystems. Refinement of our understanding of Ca and Sr uptake and allocation in trees allows improvement in the use of Ca/Sr and ⁸⁷Sr/⁸⁶Sr ratios to trace Ca sources to plants.     

Coupled Nitrogen and Calcium Cycles in Forests of the Oregon Coast Range

Nitrogen (N) is a critical limiting nutrient that regulates plant productivity and the cycling of other essential elements in forests. We measured foliar and soil nutrients in 22 young Douglas-fir stands in the Oregon Coast Range to examine patterns of nutrient availability across a gradient of N-poor to N-rich soils. N in surface mineral soil ranged from 0.15 to 1.05% N, and was positively related to a doubling of foliar N across sites. Foliar N in half of the sites exceeded 1.4% N, which is considered above the threshold of N-limitation in coastal Oregon Douglas-fir. Available nitrate increased five-fold across this gradient, whereas exchangeable magnesium (Mg) and calcium (Ca) in soils declined, suggesting that nitrate leaching influences base cation availability more than soil parent material across our sites. Natural abundance strontium isotopes (⁸⁷Sr/⁸⁶Sr) of a single site indicated that 97% of available base cations can originate from atmospheric inputs of marine aerosols, with negligible contributions from weathering. Low annual inputs of Ca relative to Douglas-fir growth requirements may explain why foliar Ca concentrations are highly sensitive to variations in soil Ca across our sites. Natural abundance calcium isotopes (δ⁴⁴Ca) in exchangeable and acid leachable pools of surface soil measured at a single site showed 1 per mil depletion relative to deep soil, suggesting strong Ca recycling to meet tree demands. Overall, the biogeochemical response of these Douglas-fir forests to gradients in soil N is similar to changes associated with chronic N deposition in more polluted temperate regions, and raises the possibility that Ca may be deficient on excessively N-rich sites. We conclude that wide gradients in soil N can drive non-linear changes in base-cation biogeochemistry, particularly as forests cross a threshold from N-limitation to N-saturation. The most acute changes may occur in forests where base cations are derived principally from atmospheric inputs.     

Distinguishing sources of base cations in irrigated and natural soils: evidence from strontium isotopes

Strontium isotope ratios (⁸⁷Sr/⁸⁶Sr) of soil solids, soil cation extracts, irrigation water and plant material are used to determine strontium and therefore cation sources and fluxes in irrigated and natural soil–plant systems. Strontium isotopes of soil solids from four soil profiles (two irrigated vineyard soils and two 'natural' profiles from nearby reserves) show large differences between soil horizons with depth. These differences are not reflected in ⁸⁷Sr/⁸⁶Sr ratios of soil labile cations, which show both little variation down-profile and much lower ratios than soil solids. In the undisturbed, natural soil profiles, labile cation ⁸⁷Sr/⁸⁶Sr ratios are close to the ratio of modern seawater, indicating that solutes of marine origin from precipitation are the primary input of strontium (and calcium) to the labile cation pool. In the irrigated soil profiles, ⁸⁷Sr/⁸⁶Sr ratios of labile cations are consistently shifted towards that of the irrigation water. Mass-balance calculations using ⁸⁷Sr/⁸⁶Sr ratios of the different inputs to the labile cation pool indicate more than 90% of labile strontium is derived from precipitation solutes in unirrigated soils, and up to 44% from irrigation water solutes as an additional source in irrigated soils. The ⁸⁷Sr/⁸⁶Sr ratios of grapes grown in irrigated soils match precisely with those of the labile soil cations, demonstrating that cation nutrients are drawn wholly from the labile cation pool and have the same mix of precipitation, irrigation, and soil solid sources. The ⁸⁷Sr/⁸⁶Sr ratios of grapes grown in the irrigated soils may therefore vary over time depending on (1) the changing mix of irrigation water and local precipitation and (2) potential change to irrigation water. These findings suggest limitations to the use of strontium isotopes in the tracing of grapes and wines to their soil of origin.     

Use of strontium isotopes and foliar K content to estimate weathering of biotite induced by pine seedlings colonised by ectomycorrhizal fungi from two different soils

Pinus sylvestris seedlings, colonised by ectomycorrhizal (EM) fungi from either of two different soils (untreated forest soil and a limed soil from a clear cut area), were grown with or without biotite as a source of K. The biotite was naturally enriched in ⁸⁷Sr and the ratio of ⁸⁷Sr/ ⁸⁶Sr in the plant biomass was estimated and used as a marker for biotite weathering and compared to estimates of weathering based on foliar content of K. Different nutrient regimes were used to expose the seedlings to deficiencies of K with and without an application of nitrogen (NH₄NO₃) in excess of seedling demand. The seedlings were grown for 220 days and the elemental composition of the shoots were analysed at harvest. The EM colonisation was followed by analysing the concentration of ergosterol in the roots and the soils. Bacterial activity of the soil was estimated by the thymidine incorporation technique. The concentration of organic acids in the soil solution was measured in the soil in which seedlings colonised by EM fungi from the untreated forest soil were grown. It was found that seedlings colonised by EM fungi from untreated forest soil had taken up more K in treatments with biotite addition compared to seedlings colonised by EM fungi from the limed forest soil (p<0.05). Seedlings from untreated forest soil had larger shoots and contained more K when grown with biotite compared to KCl as K source, indicating that biotite had a stimulatory effect on the growth of these seedlings which was not related to K uptake. Seedlings from the limed soil, on the other hand, had similar foliar K content when grown with either biotite or KCl as K source. The larger uptake of K in seedlings from untreated forest soil was not an effect of a more developed EM colonisation of the roots since seedlings from the limed soil had a higher ergosterol concentration both in the soil and in the roots. Nutrient regimes had no significant influence on the total uptake of K but the ⁸⁷Sr/ ⁸⁶Sr isotope ratio in the plant biomass indicated that seedlings grown with excess nitrogen supply had taken up proportionally less Sr from the biotite (1.8% of total Sr content) compared to seedlings grown with a moderate nitrogen supply (5.0%). Furthermore, seedlings grown with excess nitrogen supply had a reduced fungal colonisation of roots and soil and bacterial activity was lower in these soils. The ⁸⁷Sr/ ⁸⁶Sr ratio in the plant biomass was positively correlated with fungal colonisation of the roots (r ²=0.98), which may indicate that the fungus was involved in releasing Sr from the biotite. Uptake of K from biotite was not related to the amount of organic acids in the soil solution. Oxalic acid was positively related to the amount of ergosterol in the root, suggesting that oxalic acid in the soil solution originates from the EM symbionts. The accuracy of the estimations of biotite weathering based on K uptake by the seedlings in comparison with the ⁸⁷Sr/⁸⁶Sr isotope ratio measured in the shoots is discussed. This revised version was published online in June 2006 with corrections to the Cover Date.     

Changes in Sr/Ca, Ba/Ca and 87Sr/86Sr ratios between trophic levels in two forest ecosystems in the northeastern U.S.A.

The variability and biologicalfractionation of Sr/Ca, Ba/Ca and ⁸⁷Sr/⁸⁶Srratios were studied in a soil–plant–invertebrate–bird food chain in two forested ecosystems withcontrasting calcium availability in the northeasternU.S.A. Chemical measurements were made of the soilexchange pool, leaves, caterpillars, snails, and boththe femurs and eggshells of breeding insectivorousmigratory songbirds. ⁸⁷Sr/⁸⁶Sr values weretransferred up the food chain from the soil exchangepool to leaves, caterpillars, snails and eggshellswithout modification. Adult birds were the oneexception; their ⁸⁷Sr/⁸⁶Sr values generallyreflected those of lower trophic levels at each site,but were lower and more variable, probably becausetheir strontium was derived in part from foods intropical winter habitats where lower⁸⁷Sr/⁸⁶Sr ratios are likely to predominate. Sr/Ca and Ba/Ca ratios decreased at each successive trophiclevel, supporting previous suggestions that Sr/Ca andBa/Ca ratios can be used to identify the trophic levelat which an organism is primarily feeding. The changesin Sr/Ca and Ba/Ca ratios we measured for vegetationand insects were comparable to similar measurementsmade previously (but based on single samples of eachorganism) in an alpine ecosystem. Changes in Sr/Ca andBa/Ca ratios between birds and their food have notpreviously been measured, but the values we obtainedwere similar to those for herbivorous and carnivorousmammals at similar trophic levels. Our results provideevidence that supports the use of Sr/Ca ratios in thedetermination of human paleodiets and suggests thatSr/Ca ratios may also provide a useful tool in studiesof modern food webs. Furthermore, our findings suggestthat ⁹⁰Sr from nuclear fallout will notbioaccumulate in forests and that changes in Sr/Caratios between trophic levels will need to beconsidered in some cases when using⁸⁷Sr/⁸⁶Sr as a tracer of calciumbiogeochemistry.     

Paleoceanography of the Late Cretaceous (Maastrichtian) Western Interior Seaway of North America: evidence from Sr and O isotopes

Well-preserved fossils of the Late Cretaceous Western Interior Seaway (WIS) of North America have been analyzed for Sr concentration and Sr and O isotopes in order to decipher paleosalinities and paleotemperatures. The samples are from four biofacies within the Seaway (late Maastrichtian): offshore Interior (Pierre Shale), nearshore Interior (Fox Hills Formation), brackish (reduced salinity; Fox Hills Formation) and freshwater (Hell Creek Formation). Samples were also obtained from the Severn Formation of Maryland (considered to be representative of the open ocean). All biofacies (except the freshwater) are demonstrably within the Jeletzkytes nebrascensis ammonite zone (<1 Ma duration). The ⁸⁷Sr/⁸⁶Sr ratios show significant and systematic decreases from marine (mean±1 S.D.=0.707839±0.000024) to brackish facies (mean±1 S.D.=0.707677±0.000036), consistent with dilution by freshwater with a lower ⁸⁷Sr/⁸⁶Sr ratio than seawater. Such variation disallows using the ⁸⁷Sr/⁸⁶Sr ratios of fossil shell material to assign ages to fossils from the Late Cretaceous WIS without knowledge of the salinity in which the organism grew. The Sr isotope ratios for scaphitid ammonites within a single biofacies are similar to each other and different from those for scaphites in other biofacies, implying that these organisms are restricted in their distribution during life. The ⁸⁷Sr/⁸⁶Sr values of freshwater unionid mussels range widely and are not compatible with the freshwater endmember ⁸⁷Sr/⁸⁶Sr ratio required by the trend in ⁸⁷Sr/⁸⁶Sr vs. biofacies established from the other samples. Paleosalinities for the biofacies are estimated to range from 35‰ in the open marine to a minimum of 20‰ in the brackish, based on the presence of cephalopods in all four facies and the known salinity tolerance of modern cephalopods. Producing reasonable ⁸⁷Sr/⁸⁶Sr values for the freshwater endmember of a ⁸⁷Sr/⁸⁶Sr vs. 1/[Sr] plot requires a Sr concentration 0.2-0.5 that of seawater for the dominant freshwater input to the WIS. Such high Sr concentrations (relative to seawater) are not observed in modern rivers, and we suggest that the brackish environment in the WIS arose through the mixing of freshwater and seawater in a nearshore aquifer system. Reactions of the solution with aquifer solids in this ‘subterranean estuary’ [Moore, Mar. Chem. 65 (1999) 111-125] produced brackish water with the Sr concentration and isotopic composition recorded in the brackish biofacies. δ¹⁸O values of the fossils show decreases from the marine to brackish biofacies consistent with increasing temperatures (from ∼13 to 23°C) or, if temperatures were relatively constant, to a decrease in the δ¹⁸O of the water in which the shell formed. The latter interpretation is consistent with less-than-fully marine salinities in the nearshore biofacies, but both changes in temperature and the isotopic composition of the water may have occurred in this environment.     

Imaging spectroscopy reveals the effects of topography and logging on the leaf chemistry of tropical forest canopy trees

Logging, pervasive across the lowland tropics, affects millions of hectares of forest, yet its influence on nutrient cycling remains poorly understood. One hypothesis is that logging influences phosphorus (P) cycling, because this scarce nutrient is removed in extracted timber and eroded soil, leading to shifts in ecosystem functioning and community composition. However, testing this is challenging because P varies within landscapes as a function of geology, topography and climate. Superimposed upon these trends are compositional changes in logged forests, with species with more acquisitive traits, characterized by higher foliar P concentrations, more dominant. It is difficult to resolve these patterns using traditional field approaches alone. Here, we use airborne light detection and ranging‐guided hyperspectral imagery to map foliar nutrient (i.e. P, nitrogen [N]) concentrations, calibrated using field measured traits, over 400 km² of northeastern Borneo, including a landscape‐level disturbance gradient spanning old‐growth to repeatedly logged forests. The maps reveal that canopy foliar P and N concentrations decrease with elevation. These relationships were not identified using traditional field measurements of leaf and soil nutrients. After controlling for topography, canopy foliar nutrient concentrations were lower in logged forest than in old‐growth areas, reflecting decreased nutrient availability. However, foliar nutrient concentrations and specific leaf area were greatest in relatively short patches in logged areas, reflecting a shift in composition to pioneer species with acquisitive traits. N:P ratio increased in logged forest, suggesting reduced soil P availability through disturbance. Through the first landscape scale assessment of how functional leaf traits change in response to logging, we find that differences from old‐growth forest become more pronounced as logged forests increase in stature over time, suggesting exacerbated phosphorus limitation as forests recover.     

Do deep tree roots provide nutrients to the tropical rainforest?

The contribution of deep tree roots to the nutrition of a tropicalrainforest were studied along an edaphic transect in French Guyana. Soil typeswere mapped in relation to the texture of the upper horizons and the depth ofoccurrence of the loamy saprolite. The position of mature individuals of fourcommon species, differing by they rooting depth, was identified and tree leaveswere analysed for major nutrients and strontium (Sr) isotopic ratios.On average, the range of leaf isotopic ratio (⁸⁷Sr/⁸⁶Sr= 0.714–0.716) was narrow compared to that of bulk soils(⁸⁷Sr/⁸⁶Sr = 0.72–0.77). Steep gradients ofincreasing ⁸⁷Sr/⁸⁶Sr in roots with soil depth were foundin all investigated profiles, which indicated that the flux of Sr deposited inrain and leached from the litter layer was tightly retained in the upper soillayers. Over the whole of the site, as well as within each soil unit, tree⁸⁷Sr/⁸⁶Sr ratios were very similar whatever the species,and close to litter and near-surface roots ⁸⁷Sr/⁸⁶Srratios, suggesting no or very little Sr contribution from deep tree roots.Variations of Ca and Sr concentrations in leaves were strongly correlated butnot with leaf ⁸⁷Sr/⁸⁶Sr ratios. These results support thetheory that Sr and Ca uptake and cycling are mostly superficial in tropicalrainforests.     

Strontium isotope record of the Hygophum hygomii otoliths from the European middle Miocene

⁸⁷Sr/⁸⁶Sr values from otoliths of the worldwide-distributed fish Hygophum hygomii are used for the purpose of isotope chemostratigraphy. In order to evaluate the potential of H. hygomii otoliths for strontium (Sr) isotopic studies, we first compare the ⁸⁷Sr/⁸⁶Sr ratio of current representatives of the species with that of modern sea water. Then, three fossil otoliths of H. hygomii collected in middle Miocene sediments of the Aquitaine Basin (Lafaurie locality, SW France) and the Carpathian Foredeep of the Central Paratethys (Brno-Kralovo Pole locality, SE Czech Republic) are analysed. The age inferred from the ⁸⁷Sr/⁸⁶Sr ratio at Lafaurie places the two analysed otoliths within the time interval of 15.5–15.1 Ma. This time interval matches the published early Langhian age obtained from the ⁸⁷Sr/⁸⁶Sr ratio of bivalves measured at the same locality. At the Brno-Kralovo Pole, the ⁸⁷Sr/⁸⁶Sr ratio of the analysed otolith returns a wider timespan of 14.78–13.10 Ma, falling into an interval of poor time resolution of the ⁸⁷Sr/⁸⁶Sr chemostratigraphy. Comparisons with published biostratigraphic and paleoclimatic data suggest that the analysed fossil otoliths of H. hygomii were mineralized during the late part of the Langhian, at ∼14.2 Ma. This work represents a first attempt to use otoliths for ⁸⁷Sr/⁸⁶Sr chemostratigraphy, and indicates that such a use may represent a powerful tool for testing stratigraphic correlations in the future.     

Trace element and strontium isotopic analysis of Gulf Sturgeon fin rays to assess habitat use

Trace element and ⁸⁷Sr/⁸⁶Sr isotope analyses of fish pectoral fin rays offer non-destructive methods for determining habitat use. In this study, water and fin ray samples were analyzed for Gulf Sturgeon Acipenser oxyrinchus desotoi from the Choctawhatchee River Basin (FL and AL, USA) and compared with reference samples from Atlantic Sturgeon A. o. oxyrinchus held at controlled salinities (0, 10, 33 ppt). Samples were analyzed using inductively coupled plasma mass spectrometry, with a multi-collector for ⁸⁷Sr/⁸⁶Sr. In water, Sr, Ba, Mn and Zn differed between freshwater and saline habitats, with increases in Sr and decreases in Ba, Mn and Zn. ⁸⁷Sr/⁸⁶Sr decreased upstream to downstream with lowest values in saline habitats. In the reference study, water trace element concentrations and ⁸⁷Sr/⁸⁶Sr corresponded to those in pectoral fin rays. ⁸⁷Sr/⁸⁶Sr was higher in pectoral fin ray than water, due to influence of diet, which differed with salinity. In wild fish, trace elements in pectoral fin rays indicated freshwater emigration to saline habitats primarily occurred in the second to third growth zone with some heterogeneity in the population (4% <0.3 years, 39% 0.5–1.3 years, 39% 1.5–2.3 years, 17% 2.5–3.3 years). Analyses of ⁸⁷Sr/⁸⁶Sr indicated initial locations of Gulf Sturgeon were in the middle river, with few fish in the upper or lower river. Most (74%) juvenile Gulf Sturgeon utilized more than one river region prior to freshwater emigration and 48% moved upstream temporarily based on increased ⁸⁷Sr/⁸⁶Sr. After initial freshwater emigration, fish utilized lower-river to saline habitats. Collectively, these studies demonstrate the usefulness of trace element and ⁸⁷Sr/⁸⁶Sr analyses in sturgeon pectoral fin rays.     

Seawater strontium isotope curve at the Silurian/Devonian boundary: a study of the global Silurian/Devonian boundary stratotype

Present application of ⁸⁷Sr/⁸⁶Sr chemostratigraphy to detailed stratigraphical tasks is limited by inaccurate calibration of the general seawater strontium curve to absolute as well as to relative time scales. For this reason, refinement of the general seawater strontium curve has been suggested, using mainly clearly defined global boundary stratotype sections. This study reports the first ⁸⁷Sr/⁸⁶Sr data from the global Silurian/Devonian boundary stratotype section and fills an existing 1-Ma gap in available data. Generally, the data from the stratotype fit the range interpolated from published ⁸⁷Sr/⁸⁶Sr data of the general curve, but the slight differences may suggest an existence of a high-order oscillation near the Silurian/Devonian boundary. Higher ⁸⁷Sr/⁸⁶Sr values in the Devonian part of boundary bed 20 (20-beta) may indicate an exotic material influx of recycled sediment.     

The relative uptake of Ca and Sr into tree foliage using a whole-watershed calcium addition

The use of strontium isotopes and ratios of alkaline earth elements (i.e., ⁸⁷Sr/⁸⁶Sr and Ca/Sr) to trace Ca sources to plants has become common in ecosystem studies. Here we examine the relative uptake of Ca and Sr in trees and subsequent accumulation in foliage. Using a whole-watershed Ca addition experiment at the Hubbard Brook Experimental Forest in N.H., we measured the uptake of Ca relative to Sr in foliage and roots of sugar maple (Acer saccharum), yellow birch (Betula alleghaniensis), American beech (Fagus grandifolia), and red spruce (Picea rubens). Vegetation was analyzed for Ca and Sr concentrations and the ⁸⁷Sr/⁸⁶Sr ratio. A comparison of the Ca/Sr ratio in the vegetation and the Ca/Sr ratio of the applied mineral allows for the calculation of a discrimination factor, which defines whether Ca and Sr are incorporated and allocated in the same ratio as that which is available. A discrimination factor greater than unity indicates preferential uptake of Ca over Sr; a factor less than unity reflects preferential uptake of Sr over Ca. We demonstrate that sugar maple (SM) and yellow birch (YB) have similar and small discrimination factors (1.14 ± 0.12,1σ and 1.16 ± 0.09,1σ) in foliage formation and discrimination factors of less than 1 in root formation (0.55–0.70). Uptake into beech suggests a larger discrimination factor (1.9 ± 1.2) in foliage but a similar root discrimination factor to SM and YB (0.66 ± 0.06,1σ). Incorporation into spruce foliage occurs at a much slower rate than in these other tree species and precludes evaluation of Ca and Sr discrimination in spruce foliage at this time. Understanding the degree to which Ca is fractionated from Sr in different species allows for refinement in the use of ⁸⁷Sr/⁸⁶Sr and Ca/Sr ratios to trace Ca sources to foliage. Methods from this study can be applied to natural environments in which various soil cation pools have different ⁸⁷Sr/⁸⁶Sr and Ca/Sr ratios. The results reported herein have implications for re-evaluating Ca sources and fluxes in forest ecosystems.     

Variations of bioavailable Sr concentration and 87Sr/86Sr ratio in boreal forest ecosystems

The mean depth of Sr and water uptake in mixed Norway spruce (Picea abies) and Scots pine (Pinus sylvestris) stands was investigated, using natural variations of ⁸⁷Sr/⁸⁶Sr and ¹⁸O/¹⁶O in soils in relation to depth. Three spruce-pine pairs were studied on a podzol and a peat site in Northern Sweden. Tree leaf and wood, as well as soils, soil solutions and roots below each tree were analysed for Sr and Ca concentrations and ⁸⁷Sr/⁸⁶Sr ratio. The ¹⁸O/¹⁶O ratio was also determined in xylem sap and soil solutions in relation to depth. Soil solution ¹⁸O/¹⁶O decreased in relation to depth. Comparing with xylem sap ¹⁸O/¹⁶O data indicated a deeper uptake of soil water by pine than spruce on the podzol site and a superficial uptake by both species on the peat. The ⁸⁷Sr/⁸⁶Sr ratio of bioavailable Sr generally increased in soils in relation to depth. Contrastingly, the ⁸⁷Sr/⁸⁶Sr ratio in spruce wood was generally higher than in pine wood suggesting a deeper uptake of Sr by spruce. But the ⁸⁷Sr/⁸⁶Sr ratio and concentrations of bioavailable Sr were systematically higher below spruce than below pine. In order to explain these unexpected results, we built a simple flux model to investigate the possible effects of interspecific variations in Sr cycling, soil mineral weathering and depth of Sr uptake on soil and tree ⁸⁷Sr/⁸⁶Sr ratio. At the study sites, spruce cycled in litterfall up to 12 times more strontium than pine. The use of the model showed that this difference in Sr cycling could alone explain higher isotopic signatures of trees and topsoils below spruce. Besides, high isotopic signatures of roots in the A/E horizons below spruce led us to hypothesise a species-specific weathering process. Finally, the comparison between the ⁸⁷Sr/⁸⁶Sr ratios in wood and root or soil solutions below each species suggested that the average depth of Sr and water uptake were close, but irregular variations of the Sr isotopic ratio with depth reduce the accuracy of the results. Tree species strongly influence Sr isotopic ratios in boreal forest soils through differences in Sr cycling, and possibly through specific mineral weathering.     

Linking water use and nutrient accumulation in tree island upland hammock plant communities in the Everglades National Park, USA

The tree island hammock communities in the Florida Everglades provide one of many examples of self-organized wetland landscape. However, little is understood about why these elevated tree island communities have higher nutrient concentration than the surrounding freshwater marshes. Here we used stable isotopes and elemental analysis to compare dry season water limitation and soil and foliar nutrient status in upland hammock communities of 18 different tree islands located in the Shark River Slough and adjacent prairie landscapes. We observed that prairie tree islands, having a shorter hydroperiod, suffer greater water deficits during the dry season than slough tree islands by examining shifts in foliar ??¹³C values. We also found that prairie tree islands have lower soil total phosphorus concentration and higher foliar N/P ratio than slough tree islands. Foliar ??¹⁵N values, which often increase with greater P availability, was also found to be lower in prairie tree islands than in slough tree islands. Both the elemental N and P and foliar ??¹⁵N results indicate that the upland hammock plant communities in slough tree islands have higher amount of P available than those in prairie tree islands. Our findings are consistent with the transpiration driven nutrient harvesting chemohydrodynamic model. The water limited prairie tree islands hypothetically transpire less and harvest less P from the surrounding marshes than slough tree islands during the dry season. These findings suggest that hydroperiod is important to nutrient accumulation of tree island habitats.     

Strontium isotopes (87Sr/86Sr) in terrestrial ecological and palaeoecological research: empirical efforts and recent advances in continental‐scale models

Strontium (Sr) isotope analysis can provide detailed biogeographical and ecological information about modern and ancient organisms. Because Sr isotope ratios (⁸⁷Sr/⁸⁶Sr) in biologically relevant materials such as water, soil, vegetation, and animal tissues predominantly reflect local geology, they can be used to distinguish geologically distinct regions as well as identify highly mobile individuals or populations. While the application of Sr isotope analysis to biological research has been steadily increasing, high analytical costs have prohibited more widespread use. Additionally, accessibility of this geochemical tool has been hampered due to limited understanding of (i) the degree to which biologically relevant materials differ in their spatial averaging of ⁸⁷Sr/⁸⁶Sr ratios, and (ii) how these differences may be affected by lithologic complexity. A recently developed continental‐scale model that accounts for variability in bedrock weathering rates and predicts Sr isotope ratios of surface water could help resolve these questions. In addition, if this ‘local water’ model can accurately predict ⁸⁷Sr/⁸⁶Sr ratios for other biologically relevant materials, there would be reduced need for researchers to assess regional Sr isotope patterns empirically. Here, we compile ⁸⁷Sr/⁸⁶Sr data for surface water, soil, vegetation, and mammalian and fish skeletal tissues from the literature and compare the accuracy with which the local water model predicts Sr isotope data among these five materials across the contiguous USA. We find that measured Sr isotope ratios for all five materials are generally close to those predicted by the local water model, although not with uniform accuracy. Mammal skeletal tissues are most accurately predicted, particularly in regions with low variability in ⁸⁷Sr/⁸⁶Sr predicted by the local water model. Increasing regional geologic heterogeneity increases both the offset and variance between modelled and empirical Sr isotope ratios, but its effects are broadly similar across materials. The local water model thus provides a readily available source of background data for predicting ⁸⁷Sr/⁸⁶Sr for biologically relevant materials in places where empirical data are lacking. The availability of increasingly high‐quality modelled Sr data will dramatically expand the accessibility of this geochemical tool to ecological applications.     

Identifying calcium sources at an acid deposition-impacted spruce forest: a strontium isotope,alkaline earth element multi-tracer approach

Depletion of calcium from forest soils has important implications for forest productivity and health. Ca is available to fine feeder roots from a number of soil organic and mineral sources, but identifying the primary source or changes of sources in response to environmental change is problematic. We used strontium isotope and alkaline earth element concentration ratios of trees and soils to discern the record of Ca sources for red spruce at a base-poor, acid deposition-impacted watershed. We measured ⁸⁷Sr/⁸⁶Sr and chemical compositions of cross-sectional stemwood cores of red spruce, other spruce tissues and sequential extracts of co-located soil samples. ⁸⁷Sr/⁸⁶Sr and Sr/Ba ratios together provide a tracer of alkaline earth element sources that distinguishes the plant-available fraction of the shallow organic soils from those of deeper organic and mineral soils. Ca/Sr ratios proved less diagnostic, due to within-tree processes that fractionate these elements from each other. Over the growth period from 1870 to 1960, ⁸⁷Sr/⁸⁶Sr and Sr/Ba ratios of stemwood samples became progressively more variable and on average trended toward values that considered together are characteristic of the uppermost forest floor. In detail the stemwood chemistry revealed an episode of simultaneous enhanced uptake of all alkaline earth elements during the growth period from 1930 to 1960, coincident with reported local and regional increases in atmospheric inputs of inorganic acidity. We attribute the temporal trends in stemwood chemistry to progressive shallowing of the effective depth of alkaline earth element uptake by fine roots over this growth period, due to preferential concentration of fine roots in the upper forest floor coupled with reduced nutrient uptake by roots in the lower organic and upper mineral soils in response to acid-induced aluminum toxicity. Although both increased atmospheric deposition and selective weathering of Ca-rich minerals such as apatite provide possible alternative explanations of aspects of the observed trends, the chemical buffering capacity of the forest floor-biomass pool limits their effectiveness as causal mechanisms.     

Strontium isotope stratigraphy of the Gabbs Formation (Nevada): implications for global Norian–Rhaetian correlations and faunal turnover

The Luning and Gabbs formations in west‐central Nevada, USA represent a Late Triassic shallow marine sedimentary succession with global significance (the Gabbs Formation was a candidate for the basal Jurassic GSSP). Typically, the Norian–Rhaetian stage boundary is placed at the contact between the formations, and the Rhaetian–Hettangian boundary (the Triassic–Jurassic boundary) is within the Müller Canyon Member of the Gabbs Formation. However, the use of different biostratigraphical index‐species schemes in Norian–Rhaetian successions between Tethys and Panthalassa, the two largest ocean basins at the time, makes precise correlation problematic. Here, we compare ⁸⁷Sr/⁸⁶Sr measurements of well‐preserved carbonate shell material from Nevada to the well‐known and biostratigraphically constrained ⁸⁷Sr/⁸⁶Sr record from Tethys, where a negative excursion in ⁸⁷Sr/⁸⁶Sr is noted across the Norian–Rhaetian boundary. Our new ⁸⁷Sr/⁸⁶Sr data from the Luning and Gabbs formations reveal a comparable trend, with a sharp drop in ⁸⁷Sr/⁸⁶Sr within the Nun Mine Member of the Gabbs Formation, suggesting the position of the Norian–Rhaetian boundary is higher in the succession, and not between the Luning and Gabbs formations as previously defined. Relating the stage boundary using global isotopic signals is a useful tool for biostratigraphical correlation of successions between Tethys and Panthalassa, and for estimating the rate of faunal turnover at the Norian–Rhaetian stage boundary in comparison with the succeeding Late Triassic mass extinction. If correct, this biostratigraphical–chemostratigraphical correlation suggests that the current index groups for the Panthalassic stage boundary should be changed.     

Stable and radiogenic isotope analyses on shark teeth from the Early to the Middle Permian (Sakmarian–Roadian) of the southwestern USA

δ¹⁸O_P values and ⁸⁷Sr/⁸⁶Sr ratios were determined on disarticulated xenacanthiform, hybodontid and ctenacanthid shark tooth material from several Early Permian (Sakmarian–Kungurian) continental bone beds of northern Texas and southern Oklahoma as well as from the marine Middle Permian (Roadian) of northern Arizona. The δ¹⁸O_P values derived from the teeth of bone beds are in the range of 17.6–23.5‰ VSMOW, and are mostly depleted in ¹⁸O by 0.5–5‰ relative to proposed coeval marine δ¹⁸O_P values. This indicates an adaptation to freshwater habitats on the Early Permian coastal plain by several sharks. Distinctly higher δ¹⁸O_P values from two bone beds are attributed to significant evaporative enrichment in ¹⁸O in flood plain ponds. ⁸⁷Sr/⁸⁶Sr ratios of around 0.71077 are notably more radiogenic than ⁸⁷Sr/⁸⁶Sr of contemporaneous seawater. In contrast, the isotopic composition of teeth from the marine Kaibab Formation is characterised by low δ¹⁸O_P values in the range of 13.4–15.6‰ VSMOW while ⁸⁷Sr/⁸⁶Sr ratios of around 0.70821 are closer to the Roadian seawater value. The distinctly depleted δ¹⁸O_P values cannot be readily explained by fluvially affected freshening in a nearshore marine environment, so a diagenetic alteration of the Kaibab material seems to be more likely, excluding it from further interpretation.     

Long-term records of strontium isotopic composition in tree rings suggest changes in forest calcium sources in the early 20th century

Many studies made in Europe and North America have shown an increasing depletion of exchangeable base cations that may cause tree nutritional deficiencies in sensitive soils. We use radial variation of strontium isotope in tree-rings (⁸⁷Sr/⁸⁶Sr ratio) to monitor possible changes in Ca sources for tree nutrition (Sr is used as an analog to Ca). The two main sources of Ca in forest stands are mineral weathering release and atmospheric inputs. Measurements in several forest stands in temperate regions show a steep decrease from pith to outer wood of the Sr isotope ratio from∼1870 to∼1920 except for stands developed on soils with a higher Ca status. This suggests a decrease of the weathering contribution (high ⁸⁷Sr/⁸⁶Sr ratio) when cations are displaced from the soil exchange complex by acid deposition at a rate faster than the replenishment of the cation pool by mineral weathering. This displacement enhances the atmospheric contribution, which is characterized by a low ⁸⁷Sr/⁸⁶Sr ratio. Tree-ring chronologies are an exceptional historic-timing record of chemical changes in the soil environment induced by atmospheric pollution. The reliability of the tree-ring recorder has been verified with a well-controlled nutritional perturbation in the context of a limed forest stand (with a known liming Sr isotopic signature). Our data suggest that forest ecosystems were affected by atmospheric inputs of strong acids earlier than previously thought.