Corresponding author: J. F. Mustard, Department of Geological Sciences, Brown University, Providence, RI 02912, USA. (email@example.com)
 Changes of vegetation phenology in response to climate change in the temperate forests have been well documented recently and have important implications on the regional and global carbon and water cycles. Predicting the impact of changing phenology on terrestrial ecosystems requires an accurate phenology model. Although species-level phenology models have been tested using a small number of vegetation species, they are rarely examined at the regional level. In this study, we used remotely sensed phenology and meteorological data to parameterize the species-level phenology models. We used a remotely sensed vegetation index (Two-band Enhanced Vegetation Index, EVI2) derived from the Moderate Resolution Spectroradiometer (MODIS) 8-day reflectance product from 2000 to 2010 of New England, United States to calculate remotely sensed vegetation phenology (start/end of season, or SOS/EOS). The SOS/EOS and the daily mean air temperature data from weather stations were used to parameterize three budburst models and one senescence model. We compared the relative strengths of the models to predict vegetation phenology and selected the best model to reconstruct the “landscape phenology” in New England from year 1960 to 2010. Of the three budburst models tested, the spring warming model showed the best performance with an averaged Root Mean Square Deviation (RMSD) of 4.59 days. The Akaike Information Criterion supported the spring warming model in all the weather stations. For senescence modeling, the Delpierre model was better than a null model (the averaged phenology of each weather station, averaged model efficiency = 0.33) and has a RMSD of 8.05 days. A retrospective analysis using the spring warming model suggests a statistically significant advance of SOS in New England from 1960 to 2010 averaged as 0.143 days per year (p = 0.015). EOS calculated using the Delpierre model and growing season length showed no statistically significant advance or delay between 1960 and 2010 in this region. These results suggest the applicability of species-level phenology models at the regional level (and potentially terrestrial biosphere models) and the feasibility of using these models in reconstructing and predicting vegetation phenology.
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 Long term phenological observations from the northern hemisphere provided evidence that climate change is driving shifts in vegetation phenology [Fitter and Fitter, 2002; Schwartz et al., 2006]. Vegetation start-of-season (SOS) and end-of-season (EOS) are two key phenological phases (i.e., phenophases) to determine the plant growing season length (GSL), which is an important parameter in terrestrial carbon cycle in the temperate deciduous forest [Churkina et al., 2005; Dragoni et al., 2011; Piao et al., 2007; Picard et al., 2005; Richardson et al., 2010]. Changes in phenology also feedback on the climate system through the nutrient cycle, the water cycle, the surface energy budget and the production of biogenic volatile organic compounds (BVOCs) [Peñuelas et al., 2009; Schwartz, 1996]. At the community level, shifts in the phenology of related species (e.g., flowering plants and pollinators) might cause mismatches in reproductive timing and failure to produce offspring [Bradshaw and Holzapfel, 2006]. Better modeling of vegetation phenology is thus critical to predict how the ecosystem will respond to the future climate.
 Based on these analyses, phenology models have been developed from species to global levels. At the species level, phenology models for both budburst and senescence were developed based on controlled experiments and have been tested using phenological observations of dominant tree species in Europe [Chuine et al., 1998; Häkkinen et al., 1998; Hänninen, 1990] and North America [Chuine et al., 2000; Richardson et al., 2006]. It should be noted that the budburst models could not only simulate budburst, but also other stages in the spring canopy development. Budburst models assume a linear relationship between the rate of growth (e.g., the rate of increase in mean leaf area) and temperature above a given threshold (“growing degree days” (GDD)). When a certain temperature accumulation threshold (“critical forcing temperature” (F*)) is reached, budburst occurs. Some models such as the spring warming model [Hunter and Lechowicz, 1992] assume that only spring and summer temperature (Jan–Jun) has an impact on the budburst while the other models such as sequential [Sarvas, 1974] and parallel models [Kramer, 1994; Landsberg, 1974] require a cold winter – the number of days with daily temperature below a certain threshold (e.g., 2°C) reaches the chilling requirement (e.g., 15 days) – to initiate the spring temperature accumulation process while the spring warming model implicitly assumes that this winter “chilling requirement” is always fulfilled. There are complex models such as Promoter-Inhibitor Model (PIM) [Schaber and Badeck, 2003] and UniChill model [Chuine, 2000], which require at least seven years of data to avoid model over-fitting. Senescence is defined as the process of leaf coloring (red or yellow).Estrella and Menzel used more than 50 years of in-situ observations of autumn senescence of four common tree species in Germany to test the relationship between commonly used criteria (e.g., summer temperature, solar radiation) and leaf senescence, and found that the criteria were not sufficient to explain the variation in leaf senescence. In contrast,Delpierre et al.  found that a combination of temperature and photoperiod was sufficient to predict the senescence date of Sessille Oak (Quercus petraea (Matt.) Liebl.) and European beech (Fagus Sylvatica). Vitasse et al.  extended this method to four dominant species in European temperate forests and found that the senescence model has good predictability for three species: Quecus petraea, Acer pseudoplatanus and Fagus sylvatica.
 At the regional and global level, phenology models are mainly used as submodels in the terrestrial biosphere models; Most of these phenology models are empirical, using either prescribed date, or a single temperature threshold or GDD without parameter optimizations using phenological observations (for details of the models see Richardson et al. ). Thus, due to their inaccurate characterization of vegetation dynamics, these phenology models applied to the regional or global scale might underestimate or overestimate the effects on the biosphere [Randerson et al., 2009]. Comparison of phenology models in 14 terrestrial biosphere models suggests that none of the models succeeded in capturing the phenology in terms of leaf area index (LAI) or carbon fluxes, and most of the models predicted an earlier SOS and later EOS, resulting in overestimation of gross ecosystem photosynthesis by ∼20% [Richardson et al., 2012]. Comparing to these empirical models, species-level models such as the spring warming or parallel models are better supported by phenological observations [Migliavacca et al., 2012]. The species-level models are rarely tested at the regional level [Fisher et al., 2007; Picard et al., 2005]. Remote sensing provides a way to monitor several key phenological phases including leaf expansion and leaf coloring at the landscape scale (e.g. [Fisher and Mustard, 2007; Fisher et al., 2006; Morisette et al., 2009; Zhang et al., 2003]). Fisher et al. used 5 years of remotely sensed phenology and climate data to parameterize the spring warming model in New England, USA. The work was limited by the short time span of the remote sensing data and thus the model was not well-fit at each individual weather station (5 years vs. 3–5 parameters per model). Now we have 11 years (as of 2010) of remotely sensed data from MODIS that allows for a more robust model fitting with data at individual stations. We assume that each weather station records the climate data for a unique mixture of vegetation, thus phenology model parameters are spatially different, but for the same station, the model parameters are temporally invariant. In the present study, we choose New England in northeastern United States as our study area to address the following questions: (1) Can species-level budburst and senescence models predict the remotely sensed phenology better than a null model (i.e., the eleven-year-averaged remotely sensed phenology of a given location)? Which budburst model is the best? (2) Is there a trend in phenology in New England in the past 50 years?
2.1. Study Area
 The study area (40°N–44°N, 69°W–76°W) encompasses southern New England extending west to east from central New York to Martha's Vineyard, Massachusetts and north to Vermont and Maine (Figure 1). It is considered as the “tension zone” between two distinct hardwood forest communities: in the north are mainly beech, birches, and maples; in the south are mainly oaks, chestnuts and hickories. The major tree species are white pine (Pinus strobus), yellow birch (Betula alleghaniensis), red maple (Acer rubrum), red oak (Quercus rubra), and white oak (Quercus alba) [Cogbill et al., 2002].
2.2. Remotely Sensed Phenology and Spatial Weighting
 We used the remotely sensed data to estimate the vegetation phenology of the study area. The 8-day 500 m MODIS surface reflectance products (code: MOD09A1) of the study area were acquired from the NASA LPDAAC (https://lpdaac.usgs.gov/). The two-band Enhanced Vegetation Index (EVI2) [Jiang et al., 2008] was calculated for each pixel from 2000 to 2010 as follows (equation (1), ρNIRis the near-infrared band reflectance,ρRED is the red band reflectance):
Unlike EVI, EVI2 uses only the near-infrared and red bands from MODIS, making it possible to extend the use of EVI2 to sensors like AVHRR. When atmospheric effects are minimal, the difference between EVI and EVI2 is insignificant when tested over various land cover/use types and different times of the season, and EVI and EVI2 do not become saturated even when LAI exceeds 5 [Jiang et al., 2008]. Band quality files and state flags with the data were used to screen the cloudy days, water surface and other erroneous pixels. Then the EVI2 time series were processed using the Savitzky-Golay Filter, which has been used to smooth vegetation index time series with erroneous spikes due to clouds [Chen et al., 2004]. The smoothed time series were fitted using a double-logistic function (equation (2)) [Fisher and Mustard, 2007; Fisher et al., 2006]:
where v(t) is the EVI2 at time t, vmin and vamp are the minimum and amplitude values of a single year and the parameters m1, n1, m2, and n2 control the shape of the curve (Figure 2). The curve-fitting procedure used was MPFIT, a robust non-linear least-square fitting method [Markwardt, 2008, downloadable from http://purl.com/net/mpfit]. Specifically, t = m1/n1 is the SOS and t = m2/n2is the EOS. The calculated SOS and EOS are the days that the vegetation index increases/decreases to the halfway point between the maximum and minimum value. This method is considered to be less sensitive to the understory species green-up [Fisher et al., 2006], which is often earlier than that of the overstory dominant species [Richardson and O'Keefe, 2009].
 We assessed the uncertainty of remotely sensed phenology modeling in two ways: ground validation (see section 2.3) and uncertainty evaluation of parameters related to SOS and EOS. We used the 1-sigma value ofm1, n1 and 1-sigma value ofm2, n2 to assess the uncertainty in SOS and EOS, respectively. Since m1 and n1 (m2 and n2) are highly correlated correlation between m1, n1; and m2, n2. data not shown), the propagation of the uncertainty to SOS and EOS should be described as σSOS and σEOS[Taylor, 1997]:
where SOS and EOS are the estimated values of a year from equation (2); (m1,m2,n1,n2) are the estimated best values of the parameters.
 The weather stations record the temperature of their surrounding area. However, the satellite pixels around the weather stations should not be considered equally valid due to different land use/cover and elevation [Fisher et al., 2007]. Thus, we gave weights to the 7 × 7 grids surrounding the weather station. The weights are based on the vegetation cover of each pixel, the distance with the central pixel (i.e., the location of weather station), and the elevation difference between the pixel and the central pixel, and the water mask. The averaged SOS and EOS were then calculated as the weighted average of the 49 pixels in the grid.
 A pure deciduous forest in New England has an annual maximum EVI2 value (vmax) close to ∼0.8, and an annual minimum EVI2 value (vmin) close to ∼0.0. Thus the Cartesian distance in the vmax − vmin space indicates the ‘deciduousness’ of a pixel: the smaller the value is (thus higher WDC), the closer the pixel is to be considered as a deciduous forest [Fisher et al., 2006]. If vmax is greater than 0.8, then vmax was set to be equal to 0.8. The deciduousness (WDC) of a pixel is (non-deciduous pixels are thus very low inWDC and readily dismissed):
The horizontal distance weight (WHD) decreases from 1 to 0 with a lapse rate of 1/7. Calculated as the Cartesian distance between the central pixel (i = 3 and j = 3, where i and j are the horizontal and vertical coordinates),
The vertical distance weight (WVD) was calculated as the difference of elevation between the central point and any point on the grid with a lapse rate of 0.02 units m−1:
The water mask weight (Wwater) equals to 0 when the pixel is recognized as water by MODIS state flag, otherwise Wwater equals to 1. The total weight (W) of each pixel on the grid is:
2.3. Ground Validation
 We used the phenology records in Harvard Forest (42.53°N–42.54°N, 72.18°W–72.19°W) to validate remotely sensed SOS and EOS. Harvard Forest is a mixed forest dominated by red maple (Acer rubrum) and red oak (Quercus rubra). Spring canopy developments of 33 species were recorded since 1990 at an interval of 3–7 days (after 2002, the total number of species in spring was reduced to nine); fall canopy developments were observed since 1991 (except 1992) and the number of species is 14 since 2002 [O'Keefe, 2000]. Eleven years of observations of A. rubrum (5 individuals were observed) and Q. rubra (4 individuals were observed) were used to compare with remotely sensed SOS and EOS. Each time, phenological metrics were recorded as the percentage comparing to the total leaves on that tree (three spring metrics and two fall metrics, 0% to 100%): BBRK (percentage of broken buds), L75 (percentage of leaves at 75% of their total size), L95 (percentage of leaves at 95% of their total size), LCOLOR (percentage of leaves that have changed color, notice that the leaves are those remaining on the tree) and LFALL (percentages of leaves that have fallen). All of the metrics for each individual were fitted using a sigmoid curve [Fisher et al., 2007, equation (9)]:
where PM(t) is the phenological metrics at time t, PMmin and PMamp is the minimum and amplitude values of the above metrics of a single year. The parameters m1, n1 control the shape of the curve. Similar to section 2.3, we calculated the date (t = m1/n1) when the metrics reach halfway between minimum and maximum to compare with the remotely sensed phenological metrics of the Harvard Forest pixel from 2000 to 2010. The date of those metrics should be interpreted as “the date when 50% of the leaves on the tree reach that stage (for example, budburst or reaches 75% of the full leaf size).”
2.4. Climate Data
 Daily temperature and photoperiod are used as climate drivers of the phenology models. Daily maximum and minimum temperature from 1999 to 2010 were acquired from NOAA National Climate Data Center (www.ncdc.noaa.gov/oa/ncdc.html). These data were processed in the following steps: first, the daily mean temperature was calculated as the average of the daily maximum and minimum temperature [Fisher et al., 2007]; second, stations with more than 15% of the data flagged as missing (“−99999” in the original dataset) were discarded. The remaining missing data were replaced by the interpolation of nearby stations using the Linear Lapse Rate Adjustment (LLRA) [Dodson and Marks, 1997]; third, we compiled the data from September to the next June as the dataset input for spring phenology models; data from June to December were compiled for fall phenology model. Stations with 5 or more years of data were included in the dataset. Stations located in the airports and croplands were manually excluded based on the examination of Google Earth images from 2000 to 2010. The total number of included weather stations is 137. In addition, we calculated the daily photoperiod for each station as a function of the latitude of the station and the day of year [Monteith and Unsworth, 2008].
2.5. Parameterization of Climatic Phenology Models
 The models we selected in this paper must be simple in terms of the number of parameters, since we only have 11 years of satellite data. Models such as the promotor-inhibitor model (PIM) [Schaber and Badeck, 2003] with more than 5 parameters were not considered. For budburst, both 1-phase (which only consider the spring temperature) and 2-phase models (which consider both the fall and next spring temperature) were considered in this study (Table 1). For the 1-phase model, we selected the spring warming model (SW), which accumulates growing degree days (GDDs) after a given DOY (which could vary spatially). For the 2-phase model, the sequential model (SEQ) calculates the GDD after the chilling requirement is fulfilled by having a certain number of low temperature days (chilling days (CD)) [Chuine et al., 1998; Kramer, 1994; Landsberg, 1974; Sarvas, 1974]. The parallel model (PAR) calculates the GDD concurrently with CD accumulation, and budburst happens when both heating and chilling requirements are fulfilled [Chuine et al., 1998; Landsberg, 1974].
Table 1. Summary of Model Equations and Notations Used in this Study, and the Temporal Range of Temperature and Photoperiod Records Required by the Models
Sf is the accumulated heat forcing units (unit: °C); Rf is the rate of heat forcing (unit: °C/day); Sc the accumulated chilling units (unit: °C); Rf is the rate of chilling (unit: °C/day); xt is the temperature at time t; Theat, base temperature (unit: °C) required by heat accumulation process; Tchill is base temperature (unit: °C) required by chilling accumulation process; t0 is the starting date (day of year, unit: day) of accumulation; tb is the date of budburst (day of year, unit: day); th is the date when the heating accumulation is completed (day of year, unit: day); ts is the date of senescence (day of year, unit: day); F* is the critical threshold of heating process (budburst) (unit: °C); Ctotal is critical threshold of chilling process (end of chilling, quiescence) (unit: day); Ssen is the accumulated forcing units for senescence (unit: °C·hour· hour−1), Rsen is the rate of forcing (unit: °C·hour· hour−1/day); Ycrit is the critical threshold of senescence process (senescence) (unit: °C·hour· hour−1); Pstart is the photoperiod threshold for senescence process (unit: hour); P(t) is the photoperiod for day t; x, y are parameters for the DM model. Functions: max() returns the larger value of the two in the parenthesis, min() returns the smaller value in the parenthesis, while binary() return 0 if the value in the parenthesis is 0, otherwise returns 1.
Spring is from 1 January to 30 June. Autumn is from 1 August to 31 December.
SW: where Rf = max(0, xt − Theat) when Sf ≥ F* budburst occurs
Ctotal, Theat, Tchill, F*
SEQ: where Rc = binary(max(0, Tchill − xt)) when Sc ≥ Ctotal heat accumulation starts then where Rf = max(0, xt − Theat) when Sf ≥ F* budburst occurs
Ctotal, Theat, Tchill, F*
PAR: where Rc = binary(max(0, Tchill − xt)) Km = min(Sc/Ctotal, 1) and where Rf = max(0, xt − Theat) when Sf ≥ F* budburst occurs
Pstart, Tchill, x, y, Ycrit.
DM: If P(d) ≤ Pstart and xt ≤ Tchill, then where Rsen(xt) = [Tchill − xt]x × [P(t)/Pstart]y when Ssen ≥ Ycrit senescence occursc
 For senescence models, we tested the Delpierre model (DM) that assumes both temperature and photoperiod control the senescence process [Delpierre et al., 2009; Vitasse et al., 2009]. The accumulation of cold degree days (CDDs) is initiated when daily temperature and photoperiod are both below their threshold. We made a change to the DM model such that both the parameter for temperature (x) and photoperiod (y) could accept any value between 0 and 2 (Table 2) instead of only 0, 1 and 2 as in Delpierre et al. .
 The remotely sensed phenology (SOS and EOS) and the daily environmental data (temperature and photoperiod) were used to calculate the phenology model parameters (for parameters see Table 1). For each weather station, at least 5 years of data were used in the model calibration. Since we assumed that the phenology model parameters at each station is temporally invariant but spatially different from stations at other locations due to biotic factors (genotypes, species composition), models were fit individually at each weather station.
where N is the number of years of each station, tphenoobservation(yeari)is the estimated date of a phenophase (i.e., SOS and EOS) at a given year i, tphenomodel(yeari)is the modeled date of a phenophase at a given year i.
2.6. Model Evaluation
 Model accuracy and efficiency were analyzed using the RMSD (equation (10)), Nash-Sutcliffe model efficiency coefficient (ME) [Nash and Sutcliffe, 1970] (equation (11)), and Akaike Information Criterion (AIC) [Akaike, 1974]. RMSD describes the difference between the modeled phenophase date and the observed phenophase date. ME compares the phenology models with the null model (i.e., only calculating the interannual variation). ME was calculated with the following equation:
where is the averaged date of budburst or senescence. A positive ME means the models are better than a null model.
 While the best model should have the as low an RMSE as possible, it is equally important that the data are fit with the fewest model parameters (“Occam's razor”) [Burnham and Anderson, 2002]. AIC takes into account the goodness-of-fit as well as the complexity of the model. When the number of parameters (p) is large comparing to the sample size (n) (generally when n/p < 40), the small sample AIC should be used (AICc) [e.g., Migliavacca et al., 2012]:
where n is the number of observations, σ is the RMSD, p is the number of parameters. The model with the lowest AICc is considered to be the best model among the candidates. The difference of AICc scores between the best model and the other models, ΔAICc, is a measure of relative strength of the models compared to the best model. If ΔAICc < 2, then the model is considered to be close to the best model, while if ΔAICc > 6, then the model is 20 times less likely to be the best model [Migliavacca et al., 2012].
2.7. Retrospective Analysis
 Based on these metrics, the best budburst model and senescence model for the study area was identified and we chose the stations with ME higher than 0.4 for a retrospective analysis. Climate data from year 1960 to 2010 were the input to the calibrated models to derive the SOS, EOS and subtract EOS with SOS to get GSL in each year. The SOS, EOS and GSL were then averaged across the region and linear regressions of these phenophases against year were calculated.
3.1. Remotely Sensed Phenology and Uncertainty Analysis
Figure 1 shows the spatial distribution of SOS, EOS and GSL in 2002, which is similar to the other analysis for this region [Fisher and Mustard, 2007; Zhang et al., 2003]. Spatial variations in SOS and EOS show a coastal-continental gradient with altitude as a controlling factor. The late SOS in the upper Cape Cod, Martha's Vineyard and Long Island are mainly due to the concentration of scrub oak (Quecus ilicifoli) in these areas (data not shown) [Foster et al., 2002]. Scrub oak also showed an earlier EOS in the same areas (Figure 1c), together resulting in a shorter GSL.
 We assessed the quality of remotely sensed phenology by (1) evaluating the uncertainty of curve-fitting; (2) comparing with ground observations in Harvard Forest.Figure 2shows two examples of curve-fitting and the uncertainties in the estimates of SOS and EOS at the MODIS pixel covering the Harvard Forest (42.535N, 72.185W).Figure 2a is year 2010 with a low scatter and Figure 2b is year 2007 with a higher scatter. The uncertainty in SOS is smaller than that of EOS. Figure 3 shows the spatial distribution of the averaged (2000–2011) uncertainties of SOS and EOS, and both shared a similar spatial pattern: the uncertainties are generally lower along the south shore, in Adirondack Mountains and in Vermont and West Massachusetts. The uncertainties are higher over croplands on the southwest corner. The averaged uncertainty of SOS (2000–2010) of the whole study area in 2.571 days with standard deviation of 0.808 days; The averaged uncertainty of EOS (2000–2010) of the whole study area is 4.458 days with standard deviation of 1.598 days. Figure 4 shows the comparison between remotely sensed phenology and Harvard Forest ground observations. Those metrics should be interpreted as when 50% of the leaves on the tree reach the state, for example, 50% of the leaves on the tree reach their 75% size comparing to the full size (L75). L75 (r2 = 0.6428) is best in tracking the remotely sensed SOS comparing to L95 (r2 = 0.4424) and BBRK (r2 = 0.2134). Due to the large variations of fall phenological metrics, the correlation between remotely sensed EOS and LFALL/LCOLOR is not statistically significant.
3.2. Model Performance
 Among the three budburst models we tested, the spring warming model showed the best performance in terms of RMSD, AICc and ME. The budburst models showed an average RMSD less than 5 days (Table 3). The averaged RMSD and R2 values of the three models are close (Figure 5, Figure 6). However, the AICc scores of all the stations (Table 3, a total of 128 stations, 9 stations with only 5 years' data were excluded because it will cause a zero denominator) support the spring warming model, only for two stations can the PAR model be considered to be approximately equal to spring warming model (ΔAICc < 2), and more than 3/4 (100/128 and 97/128 for SEQ and PAR, respectively) of the stations are less than 20 times to be the true model. Model predictability varies across the region (Figures 7a–7c). Stations with highest RMSD were mainly distributed in the coastal area and the low elevation stations near the metropolitan Boston. The senescence model (i.e., DM) showed a higher overall and averaged RMSD than the budburst models though similarly showed high RMSD stations were mainly in the coastal area. Stations with the lowest RMSD were distributed in the inland high elevation areas. The averaged ME for the four tested models were listed in Table 3. The spring warming model was most efficient comparing to a null model which only represents the averaged start/end of season at each weather station. Both the sequential and parallel models were on average better than a null model but in some specific weather stations the ME is below zero. In a similar way to RMSD, the SW and PAR models have better performance than the SEQ model. DM had a better performance than the null model both in average and for each weather station.
Table 3. Summary of the Root Mean Square Deviation (RMSD), Model Efficiency (ME) and the Small Sample-Corrected Akaike Information Criterion (AICc) of the Modelsa
ΔAICc < 2
ΔAICc < 6
In columns 3 and 4 the figures in parentheses are the 5 and 95 percentiles of the value from all the weather stations. For 128 stations with more than 5 years' meteorological data, columns 6, 7 and 8 show the numbers of stations for which the model is considered best in comparison to the other two; the number of station where the difference between the AICc of the model and the best model is less than 2 (ΔAICc < 2) and less than 6 (ΔAICc < 6).
4.59 (2.14, 7.78)
0.49 (0.02, 0.84)
4.91 (2.24, 8.14)
0.39 (−0.28, 0.84)
4.60 (1.73, 7.95)
0.47 (−0.07, 0.88)
8.05 (3.54, 13.65)
0.33 (0.06, 0.64)
 The model parameter distributions are shown in Figure 8. Most of the stations have a base heating temperature (Theat) requirement of 3°–5°C (Figures 8a, 8d, 8h). Theat for the spring warming model is generally skewed towards zero while those for SEQ and PAR are uniform. Spring warming models mostly start the heat accumulation (accumulation of GDD) at DOY 80–100 (about 20 March to 10 April) (Figure 8b). The base chilling temperature (Tchill) requirement for the SEQ and PAR models have a peak at ∼3°C, which is more conservative than Theat. The critical forcing temperature for the three budburst models are mostly in the range of 200°–400°C (Figures 8c, 8f, 8j). Two 2-phase models have a base chilling temperature requirement of 0°–2°C (Figures 8g, 8k). For the senescence model, the threshold photoperiod is mostly between 11 and 13 hours, which for the study area occurs between September and mid-October (Figure 8l).
3.3. Retrospect Analysis Using 50 Years of Climate Data
 We found a statistically significant advancement of SOS in New England since 1960 (Table 4 and Figure 9) of an average of 0.143 days per year (p = 0.015). The advancement rate varies from station to station from 2.4 days/decade to 0.5 days per decade (Figure 10a). The stations with earlier SOS contribute to the lower envelop while those with later SOS contributes to the upper envelop in Figure 9a. On the contrary, EOS did not show a statistically significant delay or advance in the study area (p = 0.3660). This is basically a consequence of some stations showing an advance (∼53%) while the others showing a delay (∼47%) (Figure 10b). Combined together the trend in GSL is not statistically significant (although the slope is positive: 0.0638, p = 0.4148). Similar to EOS, the rate of change for GSL varies with location, with the majority of the stations (∼70%) showing a lengthening of GSL (Figure 10c).
Table 4. Slope of the Linear Regression Using the Average SOS, EOS and GSL of All Stations With ME > 0.4 From 1960 to 2010 and the p-Value of the Slope of the Average Datesa
In column 2 the figures in parentheses are the 5th and 95th percentiles of the value.
−0.143 (−0.243, −0.052)
−0.078 (−0.488, 0.142)
0.065 (−0.341, 0.353)
4.1. Uncertainty of the Remote Sensing Observations
 The uncertainty analysis suggested that the remotely sensed phenology algorithms could possibly capture both the spring and the fall canopy change. The curve-fitting process starts with the screening of cloud-contaminated data points. In addition to the cloud tags in the MODIS reflectance products, we utilized the Savitzky-Golay filter, and the double-logistic function to smooth the EVI2 time series. This algorithm effectively constrained the shape of the curve even when there were spikes in the winter (Figure 2b). Most of the EVI2 data points are within the 95% confidence interval of the fitted curve, especially for the points in the spring and fall.
 The remotely sensed SOS tracked the interannual variations of the ground-based phenological metrics (Figure 4a). The remotely sensed SOS is more correlated to the leaf expansion than budburst, probably because that the increase of leaf area is a stronger factor for the vegetation signal measured by the satellite sensor [Carlson and Ripley, 1997]. The relationships between fall phenological metrics and remotely sensed EOS are weaker. The uncertainties in the comparison are due to (1) the different scales of the observations (ground observation track vs. satellite pixels) and (2) the diverse phenological strategies of different species within the remotely sensed pixel [Steltzer and Post, 2009]. For (1), Digital camera-based phenological observations could potentially bridge the gap between satellite and ground observations [Hufkens et al., 2012]. For (2), we found that the variations of spring phenological metrics are smaller than those of fall phenological metrics (ground observations): no statistically significant difference was observed between species and individuals in the spring (data not shown); however, the differences between red oak and red maple in terms of LCOLOR and LFALL were statistically significant (p = 0.0000). Red maple changed leaf color ∼2 weeks earlier than the red oaks (interannual average: DOY 274 vs. 290, t-test:p = 0.0000), and red oaks often retain their senescencing leaves much longer (O'Keefe, personal communication). This could increase the growing season length and delay the EOS calculated from remote sensing data, compared to the early senescencing species. However, the observed EOS is within the standard deviation of LCOLOR (Figure 4c).
4.2. Models Hypothesis and Comparison
 When applying species-level models to the regional level, one important question is whether the model parameters vary across the study area. Each species has its own phenology model parameters when tested against ground observations [Chuine, 2000; Delpierre, et al., 2009; Migliavacca et al., 2012; Richardson and O'Keefe, 2009]. Fisher et al.  tested several hypotheses by applying the phenology model at the regional level. They refuted the hypotheses that forests in different locations share some common parameters (Theat and t0) while allowing other parameter (F*) to vary. The only remaining possible hypothesis is that the model parameters are station-specific and stratified by forest type. Modeling work based on ground observations supported this hypothesis:Richardson et al. found an overestimation of spring phenology in Harvard Forest when they used well-fitted spring phenology models at the more northerly Hubbard Brook Forest. Our study further supported the hypothesis by fitting the model at each individual station, and thus improved on the previous study ofFisher et al.  for its short time span of good quality remote sensing data. Since the climate stations differ in the species type and composition, we observed that the phenology model parameters vary from station to station. This method could be extended to the areas without meteorological stations using only remotely sensed data (e.g., MODIS) and gridded climate data [Picard et al., 2005]. The phenology models we used are the models for a mixture of vegetation species, which may have different phenology strategies and thus model parameters. Although limited by the species mixture, we found that the parameters were within the range of the other studies and theories based on the controlled experiments [Chuine, 2000; Kramer, 1994]. An average base temperature for SOS in this region is ∼2.74° C, and a start date of 79, which is within the range of others' work [Chuine et al., 2000; Hänninen, 1990]. Future work needs to address the effect of species composition on both the remotely sensed phenology (especially SOS and EOS) and phenology models at regional and global scales. Data fusion using Landsat TM (resolution: 30m) and MODIS (resolution: 500m) [Fisher and Mustard, 2007; Zhu et al., 2010] could be used to track the vegetation dynamics at the scale comparable to the ground-level Forest Inventory Analysis forest plots, which provide species-composition information that can be used to understand the spatial variation of phenology model parameters.
 Model evaluation based on performance measured with RMSD, AICcand ME suggested that among the selected budburst models, the SW model was the best. We suggested that model evaluation should not only be based on the goodness-of-fit, but also the model complexity (i.e., the number of parameters). When only consider RMSD, the three budburst models are close. The RMSD of the SEQ model is statistically significantly higher than those of the SW and the PAR models (p = 0.0000) while the SW and the PAR are not statistically significantly different (p = 0.9069). However, when AICc and ME are considered in the evaluation, we found that the SW is the best choice. AICc values from all stations support the SW model (Table 3). Only fewer than 1% of the stations support that the PAR model is close to the best model – the SW. Comparing to the SW, both the SEQ and the PAR models have more parameters, which in AICc will be penalized for their more complex model structure. In addition, the averaged ME is higher for the SW model than that for the PAR model. In some weather stations, the ME of the PAR model is lower than 0 (Table 3, meaning less effective than a null model), suggesting that the PAR model only works for limited areas. This might be due to the structure of the budburst models: the SW model implicitly assumes that chilling requirements in the winter are always fulfilled, while the SEQ and the PAR models need to fulfill a certain form of chilling requirement otherwise the budburst might be delayed. Previous work based on satellite and climate data found that in North America, from 40°N northward the chilling requirements are always fulfilled [Zhang et al., 2007]. Thus, additional parameters in the model structure (i.e., parameters for the chilling part) are not necessary. In addition, a comparison of the SW, SEQ, and PAR models using ground observation data in Harvard Forest also suggests that under current climate (for period 1990–2006), the SW model is still the best choice for 1/3 of the species, and the PAR model is the second choice [Richardson and O'Keefe, 2009]. However, the SEQ and the PAR models might become better in the future as the winter temperature in Northeast US is projected to increase about 2.9°C by 2100 comparing to 1961–1990 even under lower emission scenarios [Hayhoe et al., 2007], which might cause an unmet of winter chilling requirement. For the senescence model, the DM model showed an RMSD of ∼1 week, which is higher than that of budburst models, suggesting that additional factors might contribute to the variance [Vitasse et al., 2011].
4.3. Environmental Factors in the Phenology Models
 We only used temperature as the driver in our budburst models, since it is considered to be the dominant driver in spring phenology. However, the SW model implicitly includes the photoperiod requirement by allowing the start date of heat accumulation (t0) to change [Migliavacca et al., 2012]; the start date in this region are mainly between 20 March and 10 April (Figure 8b), during which the day length is about 12–13 hours in Harvard Forest. In the spring, although some early succession species such as beech are opportunists that will respond to year-to-year variation of temperature, late succession species such as oak are adapted to the local change and are more responsive to the invariant environmental factors like photoperiod [Lechowicz, 1984; Polgar and Primack, 2011]. Recently, a budburst model explicitly includes both temperature and photoperiod as the drivers, and showed a lower RMSD than the traditional the SW models when tested against ground-observed apple blossom data [Blümel and Chmielewski, 2012]. Photoperiod could be considered as a potential parameter in budburst model in the future, although it needs to be examined if the decrease in RMSD is the result of the inclusion of photoperiod mechanism or the additional parameters (In which case, AICc should be used).
 For senescence, temperature, on average, is suggested to be more important than photoperiod in controlling the senescence process [Vitasse et al., 2011]. We found a similar result that the temperature parameter x is significantly higher than the photoperiod parameter y (t-test,p = 0.0000) (Figure 11). However, we found that the relative importance of temperature and photoperiod varies across the region, and shows no clear relationship with the latitude or elevation (Figure 12). This is possibly due to the species composition: Delpierre et al.  found that the senescence of Quecus is not modulated by photoperiod (parameter y = 0) while the senescence of Fagus is controlled by both temperature and photoperiod (parameter x = 2, y = 2).
 The spatial distributions of RMSD of the four models showed a coastal high-inland low trend. The high RMSD in the coastal region might be caused by the satellite sensor drift, ocean proximity and soil type [Fisher et al., 2007; Motzkin et al., 2002]. For budburst models, RMSDs are highest near urban areas such as Boston. This might be partly due to the urban/vegetation mixture leading to noise in the seasonal trajectory of vegetation signal [Fisher and Mustard, 2007]. In addition, anthropogenic effect such as N deposition and water availability change (not parameterized in the models) [Sherry et al., 2007] might result in the diverse response of plant phenology [Cleland et al., 2006], leading to less accurate models.
4.4. Phenological Trends in New England From 1960 to 2010
 The trends of the SOS, EOS, and GSL are divergent in direction, amplitude and the significance. The averaged advance rate of SOS in New England of 1.4 days per decade (from 1960 to 2010, with a 5% and 95% percentile of 0.5 days per decade and 2.4 days per decade) found in the retrospective analysis is close to the findings of other analysis from the U.S: field observations and retrospective analysis using the Hubbard Brook Experimental Forest (within the New England) data suggest the rate is 1.8 days per decade from 1957 to 2004 [Richardson et al., 2006]. Results from a terrestrial biosphere model (ORCHIDEE) found that a 1.6 days per decade (1980–2002) increase in northern hemisphere start of season [Piao et al., 2007]. The lilac records extending from 1956 to 2003 were incorporated in a temperature-driven spring index, which suggests an advancement of 1.2 days/per decade [Schwartz et al., 2006]. Remote sensing data from NOAA/AVHRR suggested that a 7.7 days advancement in the U.S. temperate and boreal forest in 18 years (1981–1999), i.e., 4.27 days per decade [Zhou et al., 2001]. Notice that this analysis was using a coarser resolution satellite data (8km) and the result is an average across the entire latitudinal strip. Using the same dataset (NOAA/AVHRR) but a longer time span (1982–2008), Zhu, W., et al.  found that delayed EOS rather than advanced SOS dominated the vegetation phenological shift in North America (35°N–70°N). These discrepancies could be a result of the temporal scale (in our paper the retrospective analysis used dataset from 1960 to 2010) and spatial scale (New England (40°N–44°N) vs. the entire North America). Even between 1982 and 2008, phenological shifts for SOS and EOS might not be invariant: the amplitudes of SOS advance and EOS delay were larger in 1982–1999 than those in 2000–2008 [Jeong et al., 2011]. Our results suggest that by combining remote sensing and meteorological data, instead of a single site, we could potentially reconstruct the phenology of deciduous forests in the past several decades.
 Due to the lack of long-term ground observation data of senescence in North America, we were not able to compare with the other results in the same area. However, in the similar latitude in Europe,Menzel et al.  found a diverse fall season response to temperature variations, and only 3% of the species investigated were significantly delayed in autumn, including Fagus (+0.6 days/decade) and Quercus (+1.0 days/decade) during 1951–1999 [Delpierre et al., 2009]. To improve the ability of phenology model, the characterization of vegetation senescence is an important next step [Richardson et al., 2012]. Overall, the agreement with different scales of phenology data suggests the feasibility of the models being applied to the regional scale.
 Changes in the vegetation phenology may be an indicator of climate change. Species-level phenology models are considered to be more efficient than the phenology models used in the terrestrial biosphere models when tested against ground observation data [Migliavacca et al., 2012]. Yet, species-level phenology models are rarely examined in a regional context, where remote sensing provides phenological observations covering large areas. Our results suggest among the three budburst model, the simplest model—the spring warming model—is the best: the model evaluation using AICc, RMSD and ME support the SW model instead of the SEQ and PAR models (and a null model). Similarly, the DM model was better than the fall null model at predicting the occurrence of senescence. The DM model parameters also suggested that temperature is the main driver of senescence, and photoperiod is of the second importance. We also found a statistically significant advancement of the SOS in New England (averaged advancement is 0.143 days per year) using the spring warming model and the magnitude of advancement varies from station to station. However, no significant advance or delay was observed for the EOS and the GSL in this region over the period of 1960 to 2010. Our findings suggest that species-level phenology models can be parameterized using satellite and meteorological data to construct vegetation phenology at regional scale, which can be extended to areas without meteorological stations where only remote sensing data (e.g., MODIS) and gridded climate data are available. This offers a method to improve the phenology models and support their incorporation into the terrestrial biosphere models. In addition, these results suggest the possibility that the species-level models at the regional level can be used to track plants' response to past climate and predict the response to the future climate. Future research needs to address the effect of species composition on remotely sensed phenology. Digital-camera-based phenology observations could play an important role [Richardson, 2008; Richardson et al., 2009; see also Hufkens et al., 2012] in understanding how the diverse phenological strategies of different species could affect the remotely sensed phenology. Forest Inventory Analysis (FIA) dataset [Zhu, K., et al., 2012] might help to give the detailed information of species composition of part of the area. Recent efforts to use spectroscopic method and LIDAR in tropical forest for vegetation classification could help to establish a regional-scale species distribution map [Asner and Martin, 2008, 2009]. In addition, efforts to understand the driving factors of senescence would help to improve the senescence modeling.
 We thank Dennis Baldocchi, Nicolas Delpierre, Johanna Schmitt, the Associate Editor, and an anonymous reviewer for constructive comments on an earlier version of this manuscript. We thank John O'Keefe for providing the Harvard Forest phenological data and for commenting on our revised manuscript. This research was supported by the Brown University–Marine Biological Laboratory graduate program in Biological and Environmental Sciences, Brown–ECI phenology working group, and Brown Office of International Affairs Seed Grant on phenology.