Interpreting species‐specific variation in tree‐ring oxygen isotope ratios among three temperate forest trees

Although considerable variation has been documented in tree‐ring cellulose oxygen isotope ratios (δ¹⁸O_cell) among co‐occurring species, the underlying causes are unknown. Here, we used a combination of field measurements and modelling to investigate the mechanisms behind variations in late‐wood δ¹⁸O_cell (δ¹⁸O_lc) among three co‐occurring species (chestnut oak, black oak and pitch pine) in a temperate forest. For two growing seasons, we quantified among‐species variation in δ¹⁸O_lc, as well as several variables that could potentially cause the δ¹⁸O_lc variation. Data analysis based on the δ¹⁸O_cell model rules out leaf water enrichment (Δ¹⁸O_lw) and tree‐ring formation period (Δt), but highlights source water δ¹⁸O (δ¹⁸O_sw) as an important driver for the measured difference in δ¹⁸O_lc between black and chestnut oak. However, the enriched δ¹⁸O_lc in pitch pine relative to the oaks could not be sufficiently explained by consideration of the above three variables only, but rather, we show that differences in the proportion of oxygen exchange during cellulose synthesis (p_ex) is most likely a key mechanism. Our demonstration of the relevance of some species‐specific features (or lack thereof) to δ¹⁸O_cell has important implications for isotope based ecophysiological/paleoclimate studies.     

Reconstructing the δ18O of atmospheric water vapour via the CAM epiphyte Tillandsia usneoides: seasonal controls on δ18O in the field and large‐scale reconstruction of δ18Oa

Using both oxygen isotope ratios of leaf water (δ¹⁸O_L) and cellulose (δ¹⁸O_C) of Tillandsia usneoides in situ, this paper examined how short‐ and long‐term responses to environmental variation and model parameterization affected the reconstruction of the atmospheric water vapour (δ¹⁸O_a). During sample‐intensive field campaigns, predictions of δ¹⁸O_L matched observations well using a non‐steady‐state model, but the model required data‐rich parameterization. Predictions from the more easily parameterized maximum enrichment model (δ¹⁸O_L–M) matched observed δ¹⁸O_L and observed δ¹⁸O_a when leaf water turnover was less than 3.5 d. Using the δ¹⁸O_L–M model and weekly samples of δ¹⁸O_L across two growing seasons in Florida, USA, reconstructed δ¹⁸O_a was ?12.6 ± 0.3‰. This is compared with δ¹⁸O_a of ?12.4 ± 0.2‰ resolved from the growing‐season‐weighted δ¹⁸O_C. Both of these values were similar to δ¹⁸O_a in equilibrium with precipitation, ?12.9‰. δ¹⁸O_a was also reconstructed through a large‐scale transect with δ¹⁸O_L and the growing‐season‐integrated δ¹⁸O_C across the southeastern United States. There was considerable large‐scale variation, but there was regional, weather‐induced coherence in δ¹⁸O_a when using δ¹⁸O_L. The reconstruction of δ¹⁸O_a with δ¹⁸O_C generally supported the assumption of δ¹⁸O_a being in equilibrium with precipitation δ¹⁸O (δ¹⁸O_ppt), but the pool of δ¹⁸O_ppt with which δ¹⁸O_a was in equilibrium – growing season versus annual δ¹⁸O_ppt – changed with latitude.     

The oxygen isotopic signature of soil‐ and plant‐derived sulphate is controlled by fertilizer type and water source

The oxygen isotope signature of sulphate (δ¹⁸O_sulphate) is increasingly used to study nutritional fluxes and sulphur transformation processes in a variety of natural environments. However, mechanisms controlling the δ¹⁸O_sulphate signature in soil–plant systems are largely unknown. The objective of this study was to determine key factors, which affect δ¹⁸O_sulphate values in soil and plants. The impact of an ¹⁸O‐water isotopic gradient and different types of fertilizers was investigated in a soil incubation study and a radish (Raphanus sativus L.) greenhouse growth experiment. Water provided 31–64% of oxygen atoms in soil sulphate formed via mineralization of organic residues (green and chicken manures) while 49% of oxygen atoms were derived from water during oxidation of elemental sulphur. In contrast, δ¹⁸O_sulphate values of synthetic fertilizer were not affected by soil water. Correlations between soil and plant δ¹⁸O_sulphate values were controlled by water δ¹⁸O values and fertilizer treatments. Additionally, plant δ³⁴S data showed that the sulphate isotopic composition of plants is a function of S assimilation. This study documents the potential of using compound‐specific isotope ratio analysis for investigating and tracing fertilization strategies in agricultural and environmental studies.     

δ18O‐derived incubation temperatures of oviraptorosaur eggs

In order to determine the incubation temperature of eggs laid by non‐avian dinosaurs, we analysed the oxygen isotope compositions of both eggshell carbonate (δ¹⁸O_c) and embryo bone phosphate (δ¹⁸O_p) from seven oviraptorosaur eggs with preserved in ovo embryo bones. These eggs come from the Upper Cretaceous Nanxiong Formation of Jiangxi Province, China. Oviraptorosaur theropods were selected because of their known brooding behaviour as evidenced by preserved adult specimens fossilized in brooding posture on their clutch. Incubation temperature of these embryos was estimated based on the following considerations: eggshell δ¹⁸O_c value reflects the oxygen isotope composition of egg water fluid; embryo bones precipitate from the same egg fluid; and oxygen isotope fractionation between phosphate and water is controlled by the egg temperature. A time‐dependent model predicting the δ¹⁸O_p evolution of the embryo skeleton during incubation as a function of egg temperature was built, and measured δ¹⁸O_c and δ¹⁸O_p values used as boundary conditions. According to the model outputs, oviraptorosaurs incubated their eggs within a 35–40°C range, similar to extant birds and compatible with the known active brooding behaviour of these theropod dinosaurs. Provided that both eggshell and embryo bones preserved their original oxygen isotope compositions, this method could be extended to investigate some reproductive traits of other extinct groups of oviparous amniotes.     

Oxygen isotope fractionations across individual leaf carbohydrates in grass and tree species

Almost no δ¹⁸O data are available for leaf carbohydrates, leaving a gap in the understanding of the δ¹⁸O relationship between leaf water and cellulose. We measured δ¹⁸O values of bulk leaf water (δ¹⁸O_LW) and individual leaf carbohydrates (e.g. fructose, glucose and sucrose) in grass and tree species and δ¹⁸O of leaf cellulose in grasses. The grasses were grown under two relative humidity (rH) conditions. Sucrose was generally ¹⁸O‐enriched compared with hexoses across all species with an apparent biosynthetic fractionation factor (ε_bio) of more than 27‰ relative to δ¹⁸O_LW, which might be explained by isotopic leaf water and sucrose synthesis gradients. δ¹⁸O_LW and δ¹⁸O values of carbohydrates and cellulose in grasses were strongly related, indicating that the leaf water signal in carbohydrates was transferred to cellulose (ε_bio = 25.1‰). Interestingly, damping factor p_exp_x, which reflects oxygen isotope exchange with less enriched water during cellulose synthesis, responded to rH conditions if modelled from δ¹⁸O_LW but not if modelled directly from δ¹⁸O of individual carbohydrates. We conclude that δ¹⁸O_LW is not always a good substitute for δ¹⁸O of synthesis water due to isotopic leaf water gradients. Thus, compound‐specific δ¹⁸O analyses of individual carbohydrates are helpful to better constrain (post‐)photosynthetic isotope fractionation processes in plants.     

Variation in the carbon and oxygen isotope composition of plant biomass and its relationship to water‐use efficiency at the leaf‐ and ecosystem‐scales in a northern Great Plains grassland

Measurements of the carbon (δ¹³C_m) and oxygen (δ¹⁸O_m) isotope composition of C₃ plant tissue provide important insights into controls on water‐use efficiency. We investigated the causes of seasonal and inter‐annual variability in water‐use efficiency in a grassland near Lethbridge, Canada using stable isotope (leaf‐scale) and eddy covariance measurements (ecosystem‐scale). The positive relationship between δ¹³C_m and δ¹⁸O_m values for samples collected during 1998–2001 indicated that variation in stomatal conductance and water stress‐induced changes in the degree of stomatal limitation of net photosynthesis were the major controls on variation in δ¹³C_m and biomass production during this time. By comparison, the lack of a significant relationship between δ¹³C_m and δ¹⁸O_m values during 2002, 2003 and 2006 demonstrated that water stress was not a significant limitation on photosynthesis and biomass production in these years. Water‐use efficiency was higher in 2000 than 1999, consistent with expectations because of greater stomatal limitation of photosynthesis and lower leaf c_i/ca during the drier conditions of 2000. Calculated values of leaf‐scale water‐use efficiency were 2–3 times higher than ecosystem‐scale water‐use efficiency, a difference that was likely due to carbon lost in root respiration and water lost during soil evaporation that was not accounted for by the stable isotope measurements.     

Modelling non‐steady‐state isotope enrichment of leaf water in a gas‐exchange cuvette environment

The combined use of a gas‐exchange system and laser‐based isotope measurement is a tool of growing interest in plant ecophysiological studies, owing to its relevance for assessing isotopic variability in leaf water and/or transpiration under non‐steady‐state (NSS) conditions. However, the current Farquhar & Cernusak (F&C) NSS leaf water model, originally developed for open‐field scenarios, is unsuited for use in a gas‐exchange cuvette environment where isotope composition of water vapour (δ_v) is intrinsically linked to that of transpiration (δ_E). Here, we modified the F&C model to make it directly compatible with the δ_v–δ_E dynamic characteristic of a typical cuvette setting. The resultant new model suggests a role of ‘net‐flux’ (rather than ‘gross‐flux’ as suggested by the original F&C model)‐based leaf water turnover rate in controlling the time constant (τ) for the approach to steady sate. The validity of the new model was subsequently confirmed in a cuvette experiment involving cotton leaves, for which we demonstrated close agreement between τ values predicted from the model and those measured from NSS variations in isotope enrichment of transpiration. Hence, we recommend that our new model be incorporated into future isotope studies involving a cuvette condition where the transpiration flux directly influences δ_v. There is an increasing popularity among plant ecophysiologists to use a gas‐exchange system coupled to laser‐based isotope measurement for investigating non‐steady state (NSS) isotopic variability in leaf water (and/or transpiration); however, the current Farquhar & Cernusak (F&C) NSS leaf water model is unsuited for use in a gas‐exchange cuvette environment due to its implicit assumption of isotope composition of water vapor (δ_v) being constant and independent of that of transpiration (δ_E). In the present study, we modified the F&C model to make it compatible with the dynamic relationship between δ_v and δ_E as is typically associated with a cuvette setting. Using an experiment conducted on cotton leaves, we show that the modified NSS model performed well in predicting the time constant for the exponential approach of leaf water toward steady state under cuvette conditions. Such a result demonstrates the applicability of this new model to gas‐exchange cuvette conditions where the transpiration flux directly influences δ_v, and therefore suggests the need to incorporate this model into future isotope studies that employ a laser‐cuvette coupled system.     

Dentine oxygen isotopes (δ18O) as a proxy for odontocete distributions and movements

Spatial variation in marine oxygen isotope ratios (δ¹⁸O) resulting from differential evaporation rates and precipitation inputs is potentially useful for characterizing marine mammal distributions and tracking movements across δ¹⁸O gradients. Dentine hydroxyapatite contains carbonate and phosphate that precipitate in oxygen isotopic equilibrium with body water, which in odontocetes closely tracks the isotopic composition of ambient water. To test whether dentine oxygen isotope composition reliably records that of ambient water and can therefore serve as a proxy for odontocete distribution and movement patterns, we measured δ¹⁸O values of dentine structural carbonate (δ¹⁸O_SC) and phosphate (δ¹⁸O_P) of seven odontocete species (n = 55 individuals) from regional marine water bodies spanning a surface water δ¹⁸O range of several per mil. Mean dentine δ¹⁸O_SC (range +21.2 to +25.5‰ VSMOW) and δ¹⁸O_P (+16.7 to +20.3‰) values were strongly correlated with marine surface water δ¹⁸O values, with lower dentine δ¹⁸O_SC and δ¹⁸O_P values in high‐latitude regions (Arctic and Eastern North Pacific) and higher values in the Gulf of California, Gulf of Mexico, and Mediterranean Sea. Correlations between dentine δ¹⁸O_SC and δ¹⁸O_P values with marine surface water δ¹⁸O values indicate that sequential δ¹⁸O measurements along dentine, which grows incrementally and archives intra‐ and interannual isotopic composition over the lifetime of the animal, would be useful for characterizing residency within and movements among water bodies with strong δ¹⁸O gradients, particularly between polar and lower latitudes, or between oceans and marginal basins.     

Nitrogen fertilization and δ18O of CO2 have no effect on 18O‐enrichment of leaf water and cellulose in Cleistogenes squarrosa (C4) – is VPD the sole control?

The oxygen isotope composition of cellulose (δ¹⁸O_Cel) archives hydrological and physiological information. Here, we assess previously unexplored direct and interactive effects of the δ¹⁸O of CO₂ (δ¹⁸O_CO2), nitrogen (N) fertilizer supply and vapour pressure deficit (VPD) on δ¹⁸O_Cel, ¹⁸O‐enrichment of leaf water (Δ¹⁸O_LW) and cellulose (Δ¹⁸O_Cel) relative to source water, and p_exp_x, the proportion of oxygen in cellulose that exchanged with unenriched water at the site of cellulose synthesis, in a C₄ grass (Cleistogenes squarrosa). δ¹⁸O_CO2 and N supply, and their interactions with VPD, had no effect on δ¹⁸O_Cel, Δ¹⁸O_LW, Δ¹⁸O_Cel and p_exp_x. Δ¹⁸O_Cel and Δ¹⁸O_LW increased with VPD, while p_exp_x decreased. That VPD‐effect on p_exp_x was supported by sensitivity tests to variation of Δ¹⁸O_LW and the equilibrium fractionation factor between carbonyl oxygen and water. N supply altered growth and morphological features, but not ¹⁸O relations; conversely, VPD had no effect on growth or morphology, but controlled ¹⁸O relations. The work implies that reconstructions of VPD from Δ¹⁸O_Cel would overestimate amplitudes of VPD variation, at least in this species, if the VPD‐effect on p_exp_x is ignored. Progress in understanding the relationship between Δ¹⁸O_LW and Δ¹⁸O_Cel will require separate investigations of p_ex and p_x and of their responses to environmental conditions.     

Oxygen isotope fractionation between crocodilian phosphate and water

Oxygen isotope compositions of phosphate (δ¹⁸O_p) were measured in tooth enamel from captive and wild individuals of 8 crocodilian species. A rough linear correlation is observed between the δ¹⁸O_p of all the studied species and the oxygen isotope composition of ambient water (δ¹⁸O_w). Differences in mean air temperature, diet and physiology could contribute significantly to the large scatter of δ¹⁸O_p values. The combination of these parameters results in a fractionation equation for which the slope (0.82) is lower than that expected (≥ 1) from predictive model equations that assume temperature and diet as fixed parameters. Taking into account large uncertainties, the observed oxygen isotope fractionation between phosphate and ambient water does not statistically differ from that formerly established for aquatic turtles. Case studies show that δ¹⁸O_p values of fossil crocodile tooth enamel can be used to discriminate between marine and freshwater living environments within a precision of about ± 2‰ only.     

The role of effective leaf mixing length in the relationship between the δ18O of stem cellulose and source water across a salinity gradient

Previous mangrove tree ring studies attempted, unsuccessfully, to relate the δ¹⁸O of trunk cellulose (δ¹⁸O_CELL) to the δ¹⁸O of source water (δ¹⁸O_SW). Here, we tested whether biochemical fractionation associated with one of the oxygen in the cellulose glucose moiety or variation in leaf water oxygen isotope fractionation (Δ_LW) can interfere with the δ¹⁸O_SW signal as it is recorded in the δ¹⁸O_CELL of mangrove (saltwater) and hammock (freshwater) plants. We selected two transects experiencing a salinity gradient, located in the Florida Keys, USA. The δ¹⁸O_CELL throughout both transects did not show the pattern expected based on that of the δ¹⁸O_SW. We found that in one of the transects, biochemical fractionation interfered with the δ¹⁸O_SW signal, while in the other transect Δ_LW differed between mangrove and hammock plants. Observed differences in Δ_LW between mangroves and hammocks were caused by a longer effective leaf mixing length (L) of the water pathway in mangrove leaves compared to those of hammock leaves. Changes in L could have caused the δ¹⁸O_CELL to record not only variations in the δ¹⁸O_SW but also in Δ_LW making it impossible to isolate the δ¹⁸O_SW signal.     

Correlating δ13C and δ18O in cellulose of trees

We measured the carbon and oxygen isotopic composition of stem cellulose of Pinus sylvestris, Picea abies, Fagus sylvatica and Fraxinus excelsior. Several sites along a transect of a small valley in Switzerland were selected which differ in soil moisture conditions. At every site, six trees per species were sampled, and a sample representing a mean value for the period from 1940 to 1990 was analysed. For all species, the mean site δ¹³C and δ¹⁸O of stem cellulose are related to the soil moisture availability, whereby higher isotope ratios are found at drier sites. This result is consistent with isotope fractionation models when assuming enhanced stomatal resistance (thus higher δ¹³C of incorporated carbon) and increased oxygen isotope enrichment in the leaf water (thus higher δ¹⁸O) at the dry sites. δ¹⁸ O-δ¹³C plots reveal a linear relationship between the carbon and oxygen isotopes in cellulose. To interpret this relationship we developed an equation which combines the above-mentioned fractionation models. An important new parameter is the degree to which the leaf water enrichment is reflected in the stem cellulose. In the combined model the slope of the δ¹⁸O-δ¹³C plot is related to the sensitivity of the p_i/p_a of a plant to changing relative humidity.     

Responses of the carbon and oxygen isotope compositions of desert plants to spatial variation in soil salinity in Central Asia

We examined the isotopic parameters in two C₃ species (Artemisia diffusa H. Krasch and Tamarix hispida Willd.) and a C₄ species [Haloxylon aphyllum (Minkw.) Iljin.] growing or planted in soils with different levels of salinity in a Central Asian desert. The oxygen isotope ratios of stem water (δ¹⁸O_stem) in T. hispida and H. aphyllum distributed in high-salinity zones were similar to the δ¹⁸O of artesian water (δ¹⁸O_artesian) and different from that in A. diffusa distributed in lower-salinity zones. This indicates that T. hispida and H. aphyllum depend on water with low salinity in the deeper soil layer, whereas A. diffusa depends on water in the shallower soil layer that would be affected by salt accumulation. The carbon isotope composition of leaf organic matter (δ¹³C_om) and oxygen isotope enrichment in leaf organic matter above stem water (Δ¹⁸O_om) were lower in A. diffusa than in the other species. The responses of δ¹³C_om and Δ¹⁸O_om to soil salinity observed for T. hispida suggest that the species decreased its transpiration rate and increased its intrinsic water-use efficiency in response to increasing soil salinity. The δ¹³C_om and Δ¹⁸O_om of H. aphyllum were higher than those of the C₃ species, and were not correlated with soil salinity, suggesting that H. aphyllum reduced its salt uptake by decreasing transpiration—even though it was able to access less saline water in the deeper soil layer. These results indicate that the water-use strategy of desert plants in high-salinity environments can be assessed based on their carbon and oxygen isotope ratios.     

Contributions of evaporation, isotopic non-steady state transpiration and atmospheric mixing on the delta18O of water vapour in Pacific Northwest coniferous forests

Changes in the ²H and ¹⁸O of atmospheric water vapour provide information for integrating aspects of gas exchange within forest canopies. In this study, we show that diurnal fluctuations in the oxygen isotope ratio (δ¹⁸O) as high as 4‰ were observed for water vapour (δ¹⁸O_vp) above and within an old‐growth coniferous forest in the Pacific Northwest region of the United States. Values of δ¹⁸O_vp decreased in the morning, reached a minimum at midday, and recovered to early‐morning values in the late afternoon, creating a nearly symmetrical diurnal pattern for two consecutive summer days. A mass balance budget was derived and assessed for the ¹⁸O of canopy water vapour over a 2‐d period by considering the ¹⁸O‐isoflux of canopy transpiration, soil evaporation and the air entering the canopy column. The budget was used to address two questions: (1) do δ¹⁸O values of canopy water vapour reflect the biospheric influence, or are such signals swamped by atmospheric mixing? and (2) what mechanisms drive temporal variations of δ¹⁸O_vp? Model calculations show that the entry of air into the canopy column resulted in an isotopically depleted ¹⁸O‐isoflux in the morning of day 1, causing values of δ¹⁸O_vp to decrease. An isotopically enriched ¹⁸O‐isoflux resulting from transpiration then offset this decreased δ¹⁸O_vp later during the day. Contributions of ¹⁸O‐isoflux from soil evaporation were relatively small on day 1 but were more significant on day 2, despite the small H₂¹⁶O fluxes. From measurements of leaf water volume and sapflux, we determined the turnover time of leaf water in the needles of Douglas‐fir trees as ≈ 11 h at midday. Such an extended turnover time suggests that transpiration may not have occurred at the commonly assumed isotopic steady state. We tested a non‐steady state model for predicting δ¹⁸O of leaf water. Our model calculations show that assuming isotopic steady state increased isoflux of transpiration. The impact of this increase on the modelled δ ¹⁸O_vp was clearly detectable, suggesting the importance of considering isotopic non‐steady state of transpiration in studies of forest ¹⁸O water balance.     

Plant's‐eye view of temperature governs elevational distributions

Explaining species geographic distributions by macroclimate variables is the most common approach for getting mechanistic insights into large‐scale diversity patterns and range shifts. However, species' traits influencing biophysical processes can produce a large decoupling from ambient air temperature, which can seriously undermine biogeographical inference. We combined stable oxygen isotope theory with a trait‐based approach to assess leaf temperature during carbon assimilation (T_L) and its departure (ΔT) from daytime free air temperature during the growing season (T_gs) for 158 plant species occurring from 3,400 to 6,150 m a.s.l. in Western Himalayas. We uncovered a general extent of temperature decoupling in the region. The interspecific variation in ΔT was best explained by the combination of plant height and δ¹³ C, and leaf dry matter content partly captured the variation in T_L. The combination of T_L and ΔT, with ΔT contributing most, explained the interspecific difference in elevational distributions. Stable oxygen isotope theory appears promising for investigating how plants perceive temperatures, a pivotal information to species biogeographic distributions.     

Genotype differences in 13C discrimination between atmosphere and leaf matter match differences in transpiration efficiency at leaf and whole‐plant levels in hybrid Populus deltoides ×nigra

¹³C discrimination between atmosphere and bulk leaf matter (Δ¹³C_lb) is frequently used as a proxy for transpiration efficiency (TE). Nevertheless, its relevance is challenged due to: (1) potential deviations from the theoretical discrimination model, and (2) complex time integration and upscaling from leaf to whole plant. Six hybrid genotypes of Populus deltoides×nigra genotypes were grown in climate chambers and tested for whole‐plant TE (i.e. accumulated biomass/water transpired). Net CO₂ assimilation rates (A) and stomatal conductance (g_s) were recorded in parallel to: (1) ¹³C in leaf bulk material (δ¹³C_lb) and in soluble sugars (δ¹³C_ss) and (2) ¹⁸O in leaf water and bulk leaf material. Genotypic means of δ¹³C_lb and δ¹³C_ss were tightly correlated. Discrimination between atmosphere and soluble sugars was correlated with daily intrinsic TE at leaf level (daily mean A/g_s), and with whole‐plant TE. Finally, g_s was positively correlated to ¹⁸O enrichment of bulk matter or water of leaves at individual level, but not at genotype level. We conclude that Δ¹³C_lb captures efficiently the genetic variability of whole‐plant TE in poplar. Nevertheless, scaling from leaf level to whole‐plant TE requires to take into account water losses and respiration independent of photosynthesis, which remain poorly documented.     

Leaf δ18O of remaining trees is affected by thinning intensity in a semiarid pine forest

Silvicultural thinning usually improves the water status of remaining trees in water‐limited forests. We evaluated the usefulness of a dual stable isotope approach (δ¹³C, δ¹⁸O) for comparing the physiological performance of remaining trees between forest stands subjected to two different thinning intensities (moderate versus heavy) in a 60‐year‐old Pinus halepensis Mill. plantation in semiarid southeastern Spain. We measured bulk leaf δ¹³C and δ¹⁸O, foliar elemental concentrations, stem water content, stem water δ¹⁸O (δ¹⁸O_{stem water}), tree ring widths and leaf gas exchange rates to assess the influence of forest stand density on tree performance. Remaining trees in low‐density stands (heavily thinned) showed lower leaf δ¹⁸O, and higher stomatal conductance (g_s), photosynthetic rate and radial growth than those in moderate‐density stands (moderately thinned). By contrast, leaf δ¹³C, intrinsic water‐use efficiency, foliar elemental concentrations and δ¹⁸O_{stem water} were unaffected by stand density. Lower foliar δ¹⁸O in heavily thinned stands reflected higher g_s of remaining trees due to decreased inter‐tree competition for water, whereas higher photosynthetic rate was largely attributable to reduced stomatal limitation to CO₂ uptake. The dual isotope approach provided insight into the early (12 months) effects of stand density manipulation on the physiological performance of remaining trees.     

Turnover time of the non‐structural carbohydrate pool influences δ18O of leaf cellulose

Certainty regarding the degree to which organic molecules exchange oxygen with local water during plant cellulose synthesis (p_ex) is necessary for cellulose oxygen isotope (δ¹⁸O_cell)‐based applications in environmental and ecological studies. However, the currently accepted notion that p_ex is a constant of ca. 0.42 appears inconsistent with biochemical theory, which predicts that marked variation may be present in p_ex, in relation to variation in the turnover time (τ) of the carbohydrate pool available for cellulose synthesis. The above prediction was tested in the present study with the analysis of data collected from leaves of Ricinus communis grown in controlled environmental conditions that varied in light intensity and vapour pressure deficit. The results revealed the existence of considerable variation in both p_ex and τ across plants in the various growth environments. Moreover, despite uncertainties in estimates of the proportion of source water in the synthesis water (p_x) and of the biochemical fractionation factor (ε_o), our experiment yielded strong evidence that p_ex exhibits a significant, positive relationship with τ, consistent with biochemical theory. The observed variation in p_ex in association with τ has important implications for the interpretation of δ¹⁸O_cell data in environmental/ecological studies.     

Contrasting water sources and water‐use efficiency in coexisting desert plants in two saline‐sodic soils in northwest China

• Soil degradation resulting from various types of salinity is a major environmental problem, especially in arid and semiarid regions. Exploring the water‐related physiological traits of halophytes is useful for understanding the mechanisms of salt tolerance. This knowledge could be used to rehabilitate degraded arid lands.
• To investigate whether different types of salinity influence the water sources and water‐use efficiency of desert plants (Karelinia caspia, Tamarix hohenackeri, Nitraria sibirica, Phragmites australis, Alhagi sparsifolia, Suaeda microphylla, Kalidium foliatum) in natural environments, we measured leaf gas exchange, leaf carbon and xylem oxygen isotope composition and soil oxygen isotope composition at neutral saline‐sodic site (NSS) and alkaline saline‐sodic site (ASS) in northwest China.
• The studied plants had different xylem water oxygen isotope compositions (δ¹⁸O) and foliar carbon isotope compositions (δ¹³C), indicating that desert plants coexist through differentiation in water use patterns. Compared to that at the NSS site, the stem water in K. caspia, A. sparsifolia and S. microphylla was depleted in ¹⁸O at the ASS site, which indicates that plants can switch to obtain water from deeper soil layers when suffering environmental stress from both salinity and alkalinisation. Alhagi sparsifolia had higher δ¹³C at the ASS site than at the NSS site, while K. caspia and S. microphylla had lower δ¹³C, which may have resulted from interspecific differences in plant alkali and salt tolerance ability.
• Our results suggest that under severe salinity and alkalinity, plants may exploit deeper soil water to avoid ion toxicity resulting from high concentrations of soluble salts in the superficial soil layer. In managed lands, it is vital to select and cultivate different salt‐tolerant or alkali‐tolerant plant species in light of local conditions.

     

High‐resolution isotope analysis of young alewife Alosa pseudoharengus otoliths: assessment of temporal resolution and reconstruction of habitat occupancy and thermal history

Otoliths of age 0 year alewife Alosa pseudoharengus collected in different Lake Michigan habitats were microsampled, and carbon and oxygen isotope ratios (δ¹⁸O_otolith and δ¹³C_otolith) of resulting microsamples were quantified. To assess the temporal resolution of the method, age and otolith growth rates were also estimated by counting otolith daily growth increments. Core and outer intra‐otolith samples averaged 36 and 23 days, respectively. Because of the accretionary nature of otolith growth, a habitat switch by a larva occurring between 0 and 18 days post‐hatch may not be recognized by this approach. Taking this temporal resolution into account, A. pseudoharengus habitat occupancy and thermal history in nearshore Lake Michigan, and a connecting drowned river‐mouth lake were documented. Comparisons between δ¹⁸O_otolith and δ¹³C_otolith profiles, and isotope values of Lake Michigan habitats suggested that movements by individual fish between a nearshore area of Lake Michigan proper and drowned river‐mouth lake habitats were rare. Some individuals evidently moved between habitats, and such movements occurred during different periods of ontogeny. Thermal reconstructions, based on δ¹⁸O_otolith values suggested that during early life (e.g. first month of life) young A.pseudoharengus appeared to inhabit microhabitats with temperatures greater than mean epilimnetic temperatures. This study demonstrates not only the utility of intra‐otolith geochemical analysis to describe the complexity of fish behaviour in fresh water but also identifies limitations of the present approach.