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Corresponding author: M. Sano, Graduate School of Environmental Studies, Nagoya University, Furo-cho, Chikusa-ku, Nagoya 464-8601, Japan. (email@example.com)
 We developed a 50-year tree ring δ18O chronology for each of three tree species (Juniperus indica, Larix griffithii, and Picea spinulosa) using a total of 12 trees (four trees per species) from the Bhutan Himalaya. Despite originating from different species sampled at two different altitudes, the δ18O chronologies are highly correlated with one another (r = 0.76–0.89). Response analyses reveal that tree ring δ18O values are controlled mainly by summer precipitation, irrespective of species. Based on these results, a robust 269-year δ18O chronology was established to reconstruct the amount of May–September precipitation based on data from four larch trees. Our tree ring δ18O data show significant correlations with those from other regions of the Himalaya and the Tibetan Plateau, indicating that common signals related to monsoon activity are recorded in the data. However, at centennial timescales, our data from Bhutan show normal conditions during the 20th century, whereas records from sites in western Nepal and the southern/eastern Tibetan Plateau show weakening trends in monsoon intensity during the last 100–200 years; the weakening trends may be the result of a reduction in the meridional sea surface temperature gradient in the Indian Ocean during this time. At continental scales, the tree ring records show that areas more from ocean basins are particularly sensitive to reduced monsoon circulation. Correlation analyses suggest that the El Niño–Southern Oscillation (ENSO) plays an important role in modulating summer precipitation. However, the teleconnected relationship disappears during the period 1951–1970, coinciding with a negative phase of the Pacific Decadal Oscillation (PDO), implying interdecadal modulation of the PDO on the influence of the ENSO on precipitation in Bhutan.
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 The climate in South Asia is governed by the Indian monsoon, which is characterized by distinct rainy and dry seasons. The potential impact of hydroclimate regime shifts under changing global climate poses substantive challenges to human activities in the region, and therefore, accurate predictions of future changes in monsoon activity are a matter of societal concern. Because instrumentally observed climate data in South Asia are temporally and spatially limited, longer records derived from paleoclimatic proxies such as tree rings, ice cores, and speleothems are invaluable to an improved understanding of the dynamics and causes of monsoon variability.
 Tree rings are one of the most reliable and useful proxies of past climate, as they provide precisely dated time series with annual time resolutions extending back centuries to millennia. Tree ring widths have been widely used to reconstruct past precipitation and temperatures in western (Indian) Himalayan regions [e.g., Singh and Yadav, 2005; Yadav, 2011; Yadav et al., 1999, 2004]. However, dendroclimatic reconstructions for the central and eastern Himalaya are rather scant, owing largely to the paucity of long meteorological records and the reduced climate sensitivity of tree ring data associated with relatively abundant rainfall. Therefore, statistically calibrated and verified reconstructions for this region (i.e., in Nepal) have been achieved so far by using a dense network of ring width data across the region [Cook et al., 2003] and by developing several chronologies from a single site based on densitometry [Sano et al., 2005]. In addition, the climatic variables used for these reconstructions [Cook et al., 2003; Sano et al., 2005] include only temperature. Recently, Cook et al.  produced a gridded spatial reconstruction of the Palmer Drought Severity Index (PDSI) over Asia, including the Himalaya. However, precipitation patterns in the central and eastern Himalaya have yet to be reconstructed. We therefore attempted to reconstruct precipitation variations in the eastern Himalaya (Bhutan) on the basis of oxygen isotopic data from tree rings. Although a network of ring width chronologies has previously been developed for the Bhutan Himalaya [Cook et al., 2010], this study presents the first data on tree ring δ18O values from this region.
 Oxygen isotope ratios of tree ring cellulose are strongly correlated with amounts of precipitation and relative humidity. The correlations stem from the following mechanisms. First, data obtained at low latitudes show that oxygen isotopic compositions of precipitation are typically correlated with amounts of precipitation [Araguás-Araguás et al., 1998; Dansgaard, 1964]. Tree cellulose synthesized using rain water is, therefore, expected to retain information on amounts of precipitation, based on the isotopic signatures of the precipitation. Second, the isotopic composition of leaf water is influenced by transpiration through stomata, which leads to preferential loss of lighter isotopes (e.g., 16O) and consequent enrichment in heavier isotopes (e.g., 18O) [e.g., McCarroll and Loader, 2004; Robertson et al., 2001; Saurer et al., 1997]. The extent to which oxygen isotopes in leaf water are enriched through transpiration is controlled by relative humidity [e.g., Saurer et al., 1997]. Therefore, collectively, oxygen isotope compositions of tree ring cellulose are mostly influenced by the δ18O values of precipitation and levels of relative humidity. On the other hand, oxygen isotopic compositions are relatively less influenced by nonclimatic factors, such as forest disturbances, which are often recorded in ring width variations [Li et al., 2011; Sano et al., 2012a, 2012b; Xu et al., 2011]. In addition, these two factors recorded in tree ring δ18O are closely related to monsoon activity (wet-dry conditions). Our previous research conducted in the Nepal Himalaya clearly indicates that oxygen isotopes are much more sensitive to the amount of summer precipitation than are ring widths [Sano et al., 2010]. The tree ring δ18O data are therefore expected to provide a basis for the reconstruction of past hydroclimatic variations related to monsoon activity in the eastern Himalaya, whereas ring width measurements fail to capture this type of climatic information [Sano et al., 2010; Xu et al., 2011]. In addition to their use in local climate reconstructions, tree ring δ18O records can be used to investigate long-term changes in atmospheric circulation patterns, such as in the Indian summer monsoon and the El Niño–Southern Oscillation (ENSO) [e.g., Liu et al., 2012; Sano et al., 2012b], as changes in moisture sources and transport processes result in different δ18O signatures of regional precipitation [Araguás-Araguás et al., 1998; Tian et al., 2007].
 Climate modeling studies reveal that the Indian summer monsoon is intensified under global warming scenarios [May, 2002; Meehl and Washington, 1993]. Sediment records from the Arabian Sea [Anderson et al., 2002] also indicate a strengthening of monsoon winds over the past several centuries. In contrast, an increasing number of tree ring δ18O studies reveal a weakening of monsoon intensity [Grießinger et al., 2011; Sano et al., 2012a; Xu et al., 2012] in the Himalaya and on the Tibetan Plateau during the last 100–200 years. Interestingly, patterns of weakening of the summer monsoon in the Himalaya and on the Tibetan Plateau may be complex, as tree ring δ18O records from the southeastern Tibetan Plateau do not show any significant trends over the last century [Liu et al., 2013; Shi et al., 2012]. These results indicate the complex nature of monsoon dynamics and suggest that the spatiotemporal coverage of paleoclimatic information must be improved to better understand long-term changes in atmospheric circulation patterns in monsoon Asia.
 In the present study, we first explore the climatic potential of 50-year tree ring δ18O chronologies derived from three different species (Juniperus indica, Larix griffithii, and Picea spinulosa) from the Bhutan Himalaya, in which virgin forests are well preserved. Based on these results, we developed a well-replicated δ18O chronology from four larch trees over the past 269 years (1743–2011 Common Era (C.E.)). This chronology is used to reconstruct the amount of precipitation during the May–September season and allows a comparison with other published tree ring δ18O chronologies from the Himalaya and the Tibetan Plateau, especially those that focus on decadal- to centennial-scale variability. We also investigate the linkage of tree ring δ18O from the Bhutan Himalaya with the ENSO.
2 Materials and Methods
2.1 Study Sites and Sampled Trees
 Sampling for the present study was conducted in September 2011 at two sites in the Lunana region of northern Bhutan (Figure 1). The sites, which are approximately 30 km distant from one other, are at different altitudes and exhibit different floras and ecological environments. The Tanza site, which is located near the alpine tree line at an altitude of 4400 m above sea level (masl), is in an open forest dominated by juniper (Juniperus indica) trees 5–10 m in height. Because of the harsh environment, single standing trees are often more than 10 m from one another. On the other hand, the Wache site, which is located at an altitude of 3500 masl, is in a relatively closed forest composed of variously sized larch (Larix griffithii) and spruce (Picea spinulosa). The mature larch and spruce from which we collected samples are approximately 20 m in height. To precisely crossdate the growth rings from the different trees, we obtained 22 cores from 14 juniper trees from the Tanza site, 29 cores from 15 larch trees from the Wache site, and 34 cores from 15 spruce trees from the Wache site. All cores were taken at breast height (1.3 m above the ground) using either a 5 or 12 mm diameter increment borer. The mean diameters at breast height for the sampled trees were 50 cm for Juniper, 80 cm for larch, and 90 cm for spruce.
2.2 Tree Ring Data
 The core samples were crossdated by visually matching ring width variations using the standard methodology outlined by Stokes and Smiley . Since patterns of ring width variation are species dependent, crossdating was performed separately for each species. After the assignment of an absolute calendar year to every growth ring, we measured the widths of all dated growth rings using the Velmex measuring system with an accuracy of 0.01 mm. To check for possible dating errors, individual ring width series were statistically compared against a master chronology derived by averaging all series using the program COFECHA [Holmes, 1983]. According to the COFECHA results, the mean correlations between individual ring width series and the master chronology were 0.38 for juniper, 0.63 for larch, and 0.47 for spruce. Although the correlations are somewhat low, especially for juniper, the reliability of our dating is supported by significant correlations of the δ18O time series data among the different trees (see below).
 We selected four cores from four different trees of each species (total of 12 trees) for isotopic analysis. The selection of trees was based on the following two criteria: (1) cores contained as many rings as possible, and (2) growth rings were wide to produce cellulose samples for isotopic analysis. Since the pooling of multiple cores from several trees prior to isotopic analysis constrains the utility of tree ring isotope series, such as evaluating interseries coherence of variation patterns [McCarroll and Loader, 2004], isotopic analyses were conducted on each of the 12 cores separately. The analyses were performed on growth rings representing the last 50 years of growth (1962–2011) in each of the 12 cores. In addition, isotopic compositions of all growth rings in the cores of the four larch trees were measured over the entire period of each core (246, 258, 267, and 269 years), and the extended larch record was used to reconstruct the amount of May–September precipitation over the past 269 years (1743–2011 C.E.). We also explored whether age-related biases appear in the larch δ18O time series by measuring the δ18O value of the youngest core sample (the shortest duration of 171 years) for the earliest period in which systematically wider rings were produced (1841–1900). As will be discussed in detail (see below), the age-related effect was not observed in the present study.
 The “plate” method was employed to isolate α-cellulose directly from a 1.0 mm thick wood plate of a transverse section, rather than obtaining cellulose from individual rings, so as to facilitate the processing of hundreds of rings simultaneously [Xu et al., 2011]. A modified method, which is based on standard protocols [Green, 1963; Loader et al., 1997], was used to extract cellulose component from whole wood. Each annual ring of cellulose in the plates was separated from adjacent rings using a razor blade under a microscope. The reliability of the plate method was examined for several species, including for larch and spruce, by Kagawa and Nakatsuka . They found no statistically significant difference between tree ring α-cellulose δ18O values obtained using the plate method and those obtained using conventional methods.
 We loaded α-cellulose samples (120–200 µg) into silver foil and determined their 18O/16O ratios using a continuous flow isotope ratio mass spectrometer (Thermo Fisher Scientific Delta V Advantage) coupled to an elemental analyzer (Thermo Fisher Scientific Thermal Conversion/Elemental Analyzer) via a Conflo III interface. The 18O/16O ratios were expressed as δ18O (‰), deviations relative to the international Vienna Standard Mean Ocean Water (VSMOW). The analytical uncertainty, derived from a total of 186 measurements of a laboratory standard material (Merck cellulose), was 0.18‰ (1σ). All δ18O series were individually normalized to have zero mean and unit variance for the common time period of 1962–2011. The resulting series were averaged for each species to construct the final chronology. To examine the strength of common variations among different trees, we computed mean interseries correlation (Rbar) and the expressed population signal (EPS) [Wigley et al., 1984], which is calculated using Rbar and the number of samples.
2.3 Climate Analyses
 Pearson's correlation coefficients between the δ18O of tree ring cellulose and monthly climate data within 1-year dendroclimatic windows (October–September) were generated for each species to identify the response of δ18O values to climate variations. A major difficulty in undertaking dendroclimatic studies in Bhutan is the paucity of long meteorological records that are necessary for climate reconstructions. Most instrumental stations in Bhutan were established after 1984, and the observations often include missing and/or inaccurate data [Eguchi and Wangda, 2011]. We therefore utilized the 0.5° × 0.5° gridded Climatic Research Unit (CRU) TS3.10 temperature and TS3.10.01 precipitation data sets (http://badc.nerc.ac.uk/data/cru) [Harris et al., 2013], instead of local meteorological data, in this study. The monthly climate values on a 0.5° grid, as derived using triangulated linear interpolation, were based on monthly observations at meteorological stations distributed globally on land areas [Harris et al., 2013]. The gridded CRU TS3.10 data (which includes our study region) covers the period 1901–2009. However, we cannot confidently use the data from the first half of the twentieth century, because of the paucity of observations in our study area. We compared monthly precipitation data of the CRU TS3.10.01 data set with those of the “Asian Precipitation–Highly Resolved Observational Data Integration Toward Evaluation of Water Resources (APHRODITE)” [Yatagai et al., 2012]; the mean correlation between the two data sets of 0.69 reasonably validates the use of the CRU TS3.10.01 data sets. A regional average of the 16 grid points located in the area from 27.0°N–29.0°N and 89.0°E–91.0°E (see Figure 1) was generated for the response analyses. Correlation coefficients between the tree ring records and the regional climatic data were computed for the common period 1962–2009 (48 years).
 An automated weather station installed at 4109 masl in Tanza village, 3 km distant from the Tanza site, provided recent observations on a variety of meteorological parameters during the 3-year period of 2008–2010. The observations were conducted as part of Japan-Bhutan joint research projects that focus mainly on glaciology. Monthly mean temperature, precipitation, and relative humidity during the 3-year period (see Figure S1 in the supporting information) provide a basis for understanding the general climate of the region. The mean annual precipitation was 762.3 mm, 70.9% of which fell in the summer monsoon season of June–September. Premonsoon (March–May) and postmonsoon (October) rainfall contributed 25.8% of the annual precipitation. The mean monthly temperature ranges from 9.3°C (July) to −3.8°C (February). The mean monthly relative humidity ranges from 90.7% (August) to 50.6% (January).
 To explore the impacts of El Niño–Southern Oscillation (ENSO) on local climate in Bhutan, our larch chronology was correlated with NINO3.4 sea surface temperatures (SSTs) derived from the HadISST1 data set [Rayner et al., 2003] for the period 1901–2011. As the relationship between the ENSO and local climate may not be temporally stable, as indicated by Liu et al.  and Wilson et al. , correlation analyses were also conducted by separating the entire period into several time spans.
3 Results and Discussion
3.1 Intraspecies and Interspecies Variations in Tree Ring δ18O
 Figure 2 shows intraspecies variations in tree ring δ18O for juniper, larch, and spruce during the past 50 years (1962–2011). The means (and standard deviations) of δ18O values calculated for individual trees range from 22.33‰ (1.24‰) to 23.08‰ (1.50‰) for juniper, 19.22‰ (1.10‰) to 19.57‰ (1.21‰) for larch, and 21.81‰ (0.99‰) to 24.34‰ (1.08‰) for spruce. The ranges of intertree mean values were 0.75‰ for juniper, 0.35‰ for larch, and 2.53‰ for spruce. Relatively higher intertree differences were observed in the spruce data. However, the variability, which is in the range of 1‰–4‰, is typical of intertree variations observed in previous studies [Leavitt, 2010]. Mean intertree correlations (Rbar) were 0.79 for juniper, 0.88 for larch, and 0.74 for spruce. We evaluated the chronology signal strength using the expressed population signal (EPS) [Wigley et al., 1984], which indicates how well the chronology estimates a theoretical infinite population. The EPS statistics (0.94 for juniper, 0.97 for larch, and 0.92 for spruce) exceed the threshold value of 0.85 in all three species, indicating that a well-replicated mean chronology can be developed for each species.
 To understand interspecies differences in tree ring δ18O values, we averaged the δ18O values of the four individual trees in each species (Figure 3). The means (and standard deviations) of δ18O values are 22.75‰ (1.22‰) for juniper, 19.40‰ (1.09‰) for larch, and 22.72‰ (0.90‰) for spruce. The mean for larch is 3.32‰ lower than that for spruce, despite the fact that these trees grow at the same site. Li et al.  also reported that the mean δ18O for larch was 1.5‰ lower than that of spruce, although their sampled trees were located at a site in northern China. We attribute the relatively lower δ18O value in larch to species-specific physiological differences. It is well known that the oxygen in carbohydrate, which is synthesized in the leaf, undergoes partial exchange with oxygen in xylem water during cellulose synthesis [e.g., Roden et al., 2000]. The fraction of carbohydrate oxygen that undergoes exchange with oxygen of xylem water, and the net fractionation factor between them are likely to be species dependent. It is also possible that differences in root depth and growing season contribute to the δ18O differences between larch and spruce.
 Although absolute δ18O values vary depending on species, the tree ring δ18O chronologies of different species are highly correlated with one another (r = 0.76–0.89), indicating that common signals related to regional climate are preserved in all three tree species. Interestingly, the correlation coefficients are lower between spruce and larch than they are between spruce and juniper, despite the fact that the spruce and larch chronologies originate from the same sampling site. Overall, the high Rbar and EPS values in larch, as compared with those in spruce and juniper, indicate that from among the trees in this study, the larch chronology is likely the most promising source of time series data for capturing past climate changes.
3.2 Climatic Signals in Tree Ring δ18O
 The climatic responses of tree ring δ18O values are generally consistent among different species, as noted by the highly significant interspecies correlations (Figure 4). However, the tree ring δ18O chronology derived from juniper shows that juniper δ18O values are negatively correlated with amounts of precipitation in June and July and positively correlated with July temperature. The larch chronology shows that larch δ18O values are negatively correlated with amounts of precipitation in June, July, and September and positively correlated with July temperature. The spruce chronology (originating from the same site as that for larch) shows that spruce δ18O values are negatively correlated with amounts of precipitation in June and July, whereas no significant correlation is observed with temperature. In addition, a composite chronology, calculated as the mean of the three chronologies, shows significant negative correlations with only June and July precipitation (data not shown).
 To determine which climatic factor most influences δ18O values at different times of the year (the amount of precipitation or temperature), each chronology was further correlated with seasonalized precipitation and temperature values. The results show that precipitation is the primary influence on variations in tree ring δ18O values in all three species (Table 1). However, the seasonal influence of precipitation on δ18O values is species specific, being June and July for juniper, May–September for larch, and May–July for spruce. Finally, only the juniper chronology shows significant correlations with seasonalized temperatures.
Table 1. Correlations Between Tree Ring δ18O and Seasonalized Precipitation and Temperatures for the Period 1962–2009a
Single and double asterisks represent significance at the p < 0.05 and p < 0.01 levels, respectively. The highest correlation for each species is highlighted in bold.
 As noted earlier, tree ring δ18O values are mostly governed by two climatic variables: the δ18O of source water (precipitation) and relative humidity [e.g., McCarroll and Loader, 2004; Robertson et al., 2001; Saurer et al., 1997]. The δ18O value of precipitation is negatively correlated with the amount of precipitation at low latitudes, which is known as the “amount effect” [Araguás-Araguás et al., 1998; Dansgaard, 1964]. Specifically, lesser amounts of precipitation correlate with higher δ18O values of the precipitation, representing a δ18O enrichment of the source water. Therefore, the negative correlations between tree ring δ18O and local precipitation can be explained by the amount effect. On the other hand, we were not able to evaluate the effect of humidity on tree ring δ18O as instrumental records for relative humidity in the area are not available. However, relative humidity levels usually correlate with rainfall, and thus, the two parameters may not be independent of one another. More specifically, lower precipitation levels are usually associated with lower relative humidity. This causes higher gradients of vapor pressure between the atmosphere and leaf interstitial spaces, leading to preferential loss of the lighter isotopes and consequent enrichment in leaf water δ18O [e.g., Robertson et al., 2001; Roden et al., 2000].
 The positive correlations between juniper tree ring δ18O and seasonalized temperatures can be explained by the following mechanism. Warmer conditions enhance evaporation of soil water, contributing to δ18O enrichment of source water that trees take up. It should also be noted that temperature usually shows a negative correlation with the amount of precipitation, indicating that temperature and precipitation may not be independent of one another. In fact, July temperatures showing significant associations with juniper and larch δ18O values are significantly correlated with July precipitation in the study region (r = −0.51, p < 0.01). Nevertheless, our overall results can be explained by the theory of oxygen isotopes in tree rings and are consistent with previous findings obtained from the Nepal Himalaya [Sano et al., 2010, 2012a] and the Tibetan Plateau [Grieβinger et al., 2011; Shi et al., 2011].
 To further confirm the reliability of the precipitation signals identified from the area averages of gridded precipitation records, we conducted a spatial correlation analysis between tree ring δ18O values and the gridded precipitation data at all grid nodes in the area of 22.0°N–32.0°N and 85.0°E–95.0°E. The highest correlations generally appear in an area that contains the sampling site, indicating that our tree ring δ18O values for all three species accurately reflect regional precipitation (Figures 5 and S2 in the supporting information). Among the different species, relatively higher correlations occur for the larch data than for the spruce and juniper data. We therefore decided to extend the larch chronology into the preinstrumental era to reconstruct the regional precipitation history over the past 269 years.
3.3 Extended Larch Chronology and Precipitation Reconstruction
 Our extended larch δ18O time series from the four trees are highly correlated with one another for the past 269 years, as seen with high running Rbar statistics (0.85–0.93) computed over 50 years lagged by 25 years (Figure 6). The EPS statistics for the δ18O data (0.96–0.98) are also sufficiently high to exceed the threshold value of 0.85 for the past 269 years. Our chronology can therefore be considered to provide a reliable estimate of the mean for tree ring δ18O in the study region.
 It has been reported that age-dependent long-term trends often appear in tree ring δ18O time series data [e.g., Esper et al., 2010; Treydte et al., 2006]. These studies have identified a decrease in δ18O values with increasing age, a common trend irrespective of locations and species. We therefore explored whether the age-related effect biases low-frequency variations in the extended larch δ18O chronology, by measuring δ18O values of the core with the shortest duration (171 rings) for the earliest period of the core (1841–1900). Regarding ring width variations, the rings in this core sample become systematically wider with a decreasing trend, whereas the rings in the core of the longest duration (269 rings) were relatively narrow and exhibited no significant trends during the common period of 1841–1900 (Figure S3a in the supporting information). We plotted δ18O time series along with a linear regression of trends for the young and old trees (Figure S3b in the supporting information). In both cases, the δ18O series do not exhibit any significant long-term trends during the common period of 1841–1900, indicating that there is no apparent age-dependent bias. Although the difference in the mean δ18O values between short- and long-duration samples was 0.86‰, the δ18O range is only slightly greater than that of 0.60‰, which is the observed δ18O range among the four larch trees used to construct the final chronology for the common period. In addition, this variability (range of 0.86‰) is on the low end of the range of approximately 1‰–4‰ and is typical of values of intertree variability as reported in the literature [Leavitt, 2010]. Therefore, the difference in the absolute values observed between young and old trees does not seem to originate from the age-related effect. In this study, the pith in all five larch cores (four old and one young tree) was absent; therefore, the cambium ages of the earliest rings are considered to exceed at least a few decades. Recently, Young et al.  and Szymczak et al.  have reported that age-dependent trends are only observed for the earliest 50 years after germination. Based on our results, together with the finding of Young et al.  and Szymczak et al. , we conclude that the age-related effect does not appear in our larch δ18O chronology.
 The fidelity of the regression model that is utilized to reconstruct the amount of May–September precipitation was scrutinized by conducting split period calibration-verification tests [Cook and Kairiukstis, 1990; Fritts, 1976], which are widely used in tree-ring-based climate reconstructions. For this analysis, an extended 60-year period of the climate data (1950–2009) was utilized to increase the degrees of freedom while attempting to eliminate possible uncertainties in the earlier period of 1901–1949 attributed to a paucity of observations. Our results showed that the reduction of error [Fritts, 1976] was positive: 0.198 for the 1950–1979 verification period and 0.406 for the 1980–2009 verification period. The coefficient of efficiency [Cook et al., 1999] was also positive: 0.183 for the 1950–1979 verification period and 0.394 for the 1980–2009 verification period. Any positive value for these two tests indicates predictive skill of the regression model; therefore, the results support the validity of the reconstruction model. We therefore reconstructed the amount of May–September precipitation back to 1743 C.E., based on a linear regression model that accounts for 30.9% of the actual precipitation variance for the period 1950–2009 (Figure 7). Overall, our reconstructed precipitation record reveals that a relatively intense monsoon period in the nineteenth century was followed by a normal period of precipitation in the twentieth century.
3.4 Comparison With Other Proxy Records
 We compared our 269-year δ18O record with previously published tree ring δ18O chronologies from the Nepal Himalaya [Sano et al., 2012a] and the Tibetan Plateau [Grießinger et al., 2011; Liu et al., 2013; Shi et al., 2012; Xu et al., 2012]. Because the samples in the different studies were collected from different elevations, species, and ecological environments, the climatic parameters and signal seasons vary in the different chronologies. Specifically, the Humla chronology from western Nepal records dry-wet conditions represented by the Palmer Drought Severity Index (PDSI) in the period June–September, while other chronologies from the Tibetan Plateau represent August precipitation [Grießinger et al., 2011], June–August [Shi et al., 2012] and July–August [Liu et al., 2013] cloud cover, and summer precipitation/humidity [Xu et al., 2012]. However, all the chronologies correlate with moisture-related climatic parameters in the summer season, indicating that tree ring δ18O data in this region is a proxy of monsoon intensity.
 As shown in Table 2, our δ18O chronology shows highly significant correlations (p < 0.0001) with those from other regions for the common period 1781–2000, except with the chronology from the eastern Tibetan Plateau [Xu et al., 2012], indicating that common signals related to monsoon activity are recorded in our record. Correlations computed after removing low-frequency variations using 50-year cubic splines [Cook and Peters, 1981] are similar to those calculated for the original chronologies. This indicates that high-frequency variations in our tree ring δ18O data are also shared by those of other chronologies. On the other hand, the correlation matrix given in Table 2 reveals that the Humla chronology from the western Nepal Himalaya [Sano et al., 2012a] and the Hongyuan chronology from the eastern Tibetan Plateau [Xu et al., 2012] are generally less correlated with other chronologies, owing to the different climatic conditions associated with the large geographic separations of the sampling sites.
Table 2. Correlation Matrix Calculated Using the Six Tree Ring δ18O Chronologies From the Himalaya and Tibet for the Common Period 1781–2000 C.E.a
The values in parentheses were computed after removing low-frequency variations using 50-year cubic splines. The superscript “ns” denotes nonsignificant correlations (p > 0.01). See Figure 1 for the locations of the sampling sites.
 All the chronologies in Table 2 are plotted in Figure 8, along with smoothed curves emphasizing 50-year variability (note that the normalized δ18O scales are inverted to fit the precipitation scales; see Figure 1 for locations of study sites). Our chronology is in good agreement with the Bomi “A” chronology [Shi et al., 2012] from the southeastern Tibetan Plateau at multidecadal scales (Figures 8a and 8b). Both chronologies show that an intense monsoon period during the nineteenth century was followed by a normal period in the twentieth century. The Bomi “B” chronology [Liu et al., 2013] also shows an intense monsoon period during the early and midnineteenth century (Figure 8c), but a notable weak monsoon period in the late nineteenth century (unlike the Bomi “A” chronology or our chronology). However, conditions during the twentieth century were normal and without any prominent trends in all three chronologies (Figures 8a, 8b, and 8c), although decadal variations in the Bomi “B” chronology differ somewhat from those of the other two chronologies from the 1980s to the present. Overall, multidecadal variations are generally shared between the Bhutan Himalaya and the southeastern Tibetan Plateau.
 In contrast, δ18O chronologies from the Nepal Himalaya [Sano et al., 2012a] and the southern [Grießinger et al., 2011] and eastern [Xu et al., 2012] Tibetan Plateau reveal a weakening of monsoon precipitation during the past 100–200 years (Figures 8d–8f). Long-term trends of decreasing precipitation are also observed in a varve thickness record from lake sediments [Chu et al., 2011] and a snow accumulation record from an ice core [Zhao and Moore, 2006] from the Tibet Plateau. In addition, analyses based on instrumental data for the last 50 years indicate a weakening of global monsoon rainfall over land [Wang and Ding, 2006; Zhou et al., 2008b]. Several studies link the reduction in monsoon precipitation with changes in SSTs in the Indian Ocean [e.g., Chung and Ramanathan, 2006; Naidu et al., 2009; Zhou et al., 2008a]. Chung and Ramanathan  reported that the 1930–1950 mean SSTs in the Bay of Bengal and northern Arabia Sea were higher than those in the equatorial Indian Ocean in June, thus facilitating the development of the Indian summer monsoon. However, since the 1950s, significant warming has been observed in the equatorial regions of the Indian Ocean, accompanied by minimal warming in its northern regions, leading to a weakening of the meridional SST gradient in the Indian Ocean [Chung and Ramanathan, 2006]. Their model simulations reveal that the weakening of the meridional SST gradient lessens monsoon circulation, resulting in reduced monsoon precipitation over India [Chung and Ramanathan, 2006]. Xu et al.  also associated a weakening of monsoon intensity, as observed in their tree ring δ18O record from the eastern Tibetan Plateau, with the decreased meridional SST gradient. The detection of a warming trend in a coral-based reconstruction of SSTs for the whole of the tropics (30°N–30°S) [Wilson et al., 2006] suggests that SST forcing is likely to explain decreasing trends in monsoon intensity over the last 100–200 years.
 Perhaps the most striking difference among the different tree ring δ18O records is the twentieth century weakening of monsoon intensity observed in the Nepal Himalaya and the southern/eastern Tibetan Plateau (Figures 8d–8f), as compared with the absence of such a trend in the Bhutan Himalaya and the southeastern Tibetan Plateau (Figures 8a–8c). Monsoon depressions normally form in the northern Bay of Bengal and move northwestward along the axis of the monsoon trough, yielding widespread rains [Pant and Rupa Kumar, 1997]. Also, water vapor originating in the Bay of Bengal moves northward along the eastern edge of the Tibetan Plateau and enters into China [Xu et al., 2012]. The depressions generally weaken with increasing distance of travel from the ocean as the systems become cut off from the moisture supply [Pant and Rupa Kumar, 1997]. As shown in Figure 1, the chronologies that show the weakening in monsoon intensity (red triangles) are located relatively further away from the Bay of Bengal than are those from Bhutan and the southeastern Tibetan Plateau where the weakening is absent (blue triangles). Thus, inland areas appear to be particularly sensitive to the weakening of monsoon circulation.
 Interestingly, the phases of low-frequency variations in the tree ring δ18O chronology from western Nepal are generally opposite those of the Bhutan Himalaya (Figure 9). Note that both chronologies were detrended using linear regression and were filtered to emphasize 100-year variability using cubic splines [Cook and Peters, 1981]. At these timescales, variations in the chronologies show a negative correlation of −0.48, while the original records show a positive correlation of 0.37. It is widely recognized that the Indian summer monsoon exhibits intraseasonal oscillations, referred to as “active” and “break” spells, which exhibit quasiperiodic variations of 10–20 days and 30–50 days [e.g., Krishnamurthy and Shukla, 2000; Pant and Rupa Kumar, 1997; Webster et al., 1998; Yasunari, 1979, 1980]. During the “break” spells, the monsoon trough moves northward to the foothills of the Himalaya, resulting in a decrease in rainfall in the central parts of India but enhanced rainfall in the Himalayan foothills of northern India [Pant and Rupa Kumar, 1997]. This pattern is reversed during the “active” spells. Empirical orthogonal function (EOF) analysis of summer monsoon precipitation data for the period 1872–1990 at 306 stations distributed across India reveals that the first EOF exhibits a dipole-type spatial structure in precipitation variability [Pant and Rupa Kumar, 1997]. Specifically, the northeastern parts of India (and the south of Bhutan) are in one phase while the remainder of the country is in the opposite phase. Therefore, a centennial-scale alternating modality of the intraseasonal oscillations (in which active or break dominates) is possibly responsible for the contrasting phase variations in the tree ring records of western Nepal and Bhutan.
3.5 ENSO Teleconnections With Precipitation in Bhutan
 The larch δ18O chronology exhibits a significant positive correlation (r = 0.50, p < 0.0001) with May–September NINO3.4 SSTs for the period 1901–2011. This result indicates that El Niño (La Niña) events are generally linked to dry (wet) conditions in the Bhutan Himalaya. In fact, the two most severe droughts in Bhutan in the twentieth century (identified by peak δ18O values) in 1972 and 1982 corresponded to major El Niño events. The ENSO-monsoon linkage has also been identified in a tree ring δ18O chronology from northern Vietnam [Sano et al., 2012b]. A striking feature in the record is a significant time-stable correlation with ENSO records for the period 1871–2004, indicating that the hydroclimate of northern Vietnam has been firmly linked to the ENSO at least since the late nineteenth century [Sano et al., 2012b].
 The influence of the ENSO on the amount of summer precipitation is known to vary temporally and spatially. Krishna Kumar et al.  revealed that the inverse relationship between the ENSO and Indian summer monsoon rainfall, which was present during the 1850s to the 1980s, has since broken down. However, the relationship between the ENSO and our tree ring δ18O record from Bhutan has remained stable during the period 1971–2011 (r = 0.61, p < 0.0001) (Figure 10a). In addition, our chronology shows a significant correlation with the ENSO for the period 1901–1950 (r = 0.49, p < 0.001), but no correspondence during 1951–1970 (r = 0.10, p = 0.69). These results indicate that the temporal influence of the ENSO on the amount of summer rainfall often differs between Bhutan and India. Liu et al.  also identified a broken relationship between the ENSO and tree ring δ18O values from southwestern China during the period 1930–1980, although they were significantly correlated with each other during the periods 1902–1930 and 1980–2004. Interestingly, the temporal patterns of the linkage with ENSO in the southwestern China study area are generally consistent with our results. Specifically, in both records, a broken linkage with the ENSO is found during the midtwentieth century; however, the two records are not exactly matched temporally.
 The period 1951–1970, during which the ENSO-rainfall linkage broke down, coincides with a negative phase of the Pacific Decadal Oscillation (PDO) during the period of 1947–1977 [Mantua et al., 1997]; moreover, the influence of the ENSO on local rainfall in Bhutan is consistent only during positive phases of the PDO (Figure 10b). Krishnan and Sugi  reported that the PDO could play an important role in modulating interannual monsoon variability. Specifically, Indian summer monsoon rainfall more often tends to be below (above) normal when El Niño (La Niña) events occur during positive (negative) phases of the PDO [Krishnan and Sugi, 2003]. A similar tendency is also found for the amount of early summer precipitation over South China [Chan and Zhou, 2005]. Krishnan and Sugi  explained that reinforced SST anomalies resulting from phase-locking of the PDO and the ENSO can alter convective and dynamical fields, producing persistent anomalies over the tropics and the monsoon region. However, our record from Bhutan does not show the tendency observed in India and South China but shows secular variations in the ENSO-rainfall linkage during the negative phase of the PDO (Figure 10b). Power et al.  also reported PDO-related secular variations. They found that the relationship between the ENSO and rainfall in Australia is not robust during positive phases of the PDO; moreover, the relationship is consistent only during negative phases of the PDO [Power et al., 1999]. Our results, together with the findings of Power et al. , imply that the PDO contributes to secular variations in the ENSO-monsoon linkage, although the physical mechanisms underlying the possible contribution have yet to be fully explored.
 Using δ18O data from four larch trees, we constructed a well-replicated 269-year δ18O chronology (1743–2011 C.E.) to reconstruct long-term variations in the amount of May–September precipitation. Our δ18O data show significant positive correlations with chronologies from other regions of the Himalaya and the Tibetan Plateau for the common period 1781–2000, indicating that common signals are recorded in the chronologies. On the other hand, at centennial timescales, a weakening in monsoon intensity has been observed in the Nepal Himalaya and the southern/eastern Tibetan Plateau, whereas no such trend has been detected in the Bhutan Himalaya or the southeastern Tibetan Plateau. Judging from the locations of tree ring records in this region, inland areas likely receive less intense summer precipitation during periods of weakened monsoon, as opposed to sites closer to the Bay of Bengal, which are not similarly affected. We also found that tree ring δ18O (and thus the amount of May–September precipitation) in the Bhutan Himalaya is closely linked to the ENSO. However, the link was not observed during 1951–1970, which coincided with a negative phase of the PDO (1947–1977), implying interdecadal modulation of the PDO on the influence of the ENSO on local precipitation in Bhutan. Future research based on an expanded network of tree ring δ18O chronologies over the Himalaya and the Tibetan Plateau will improve our understanding of the dynamics and causes of monsoon variability in South Asia.
 We are deeply indebted to the Department of Geology and Mines, the Renewable Natural Resources Research Center, and the National Biodiversity Center, Bhutan, for granting us permission to conduct this research. We thank S. Takenaka, K. Ghallay, T. Nuimura, and S. Tsutaki for generous support during fieldwork. We also thank John Bershaw, Matthew Therrell, and an anonymous reviewer for valuable comments and suggestions that improved the manuscript. This study was funded by Grants-in-Aid for Scientific Research from the Japan Society for the Promotion of Science (19253001, 2310262, and 23242047), and a research grant from the Research Institute of Humanity and Nature, Japan.