This research was conducted in April 2017 and involved eight wild populations of J. platyphylla growing under the tropical conditions of the states of Sinaloa and Durango in Northwestern Mexico (Table 1). Ripe fruit was collected to obtain the seeds; 100 seeds of each accession were washed with Axion^® detergent (Colgate-Palmolive, NY, U.S.A.) for 10 min and subsequently treated with 30% commercial sodium hypochlorite (Cloralex^®, Nuevo León, MX) for 15 min and rinsed five times with distilled water; then, a pre-germination treatment was performed in distilled water at 60˚C for one hour, and the part of the micropile was scarified. The treated seeds were placed on moistened paper for germination and incubated in a growth chamber at 25˚C ± 2˚C in dark conditions. Once germination occurred, they were seeded in 250-mL polypropylene cups, drilled on the base and with Sogemix^® substrate (Quebec, CAN). Once the plants developed, they were placed in the greenhouse under controlled light and room temperature of 28˚C ± 7˚C conditions; the seedling percentage obtained was assessed. In the pre-field stage developed in the greenhouse, complete plants were extracted from the pot; germination, emergence, appearance of true leaves and stem elongation were recorded. The plants were transplanted in open field at a distance of 2 m between plants and 3 m between rows; 60 g of triple 17 fertilizers and 1 kg of compost were applied to each plant as base fertilizer. Plants with homogeneous characteristics were selected, and stem length, number of leaves, and morphological evaluations of the different organs were recorded. For determination of stomatal index: Slides as prepared for stomatal index by using the formula,

Stomatal index (%) = (S/S + E) × 100 (1)

where, S and E are the number of stomata and epidermal cells respectively in microscopic view field. Like stomatal density, stomatal index (%) can be calculated for both the surfaces of leaves [17]. Three-month plants were used and planted in an experimental plot located in the community La Campana, Culiacán, Sinaloa (24˚59'28"N and 107˚34'25"W) at 97 m a.s.l.

Daily weather variables were recorded in an automated station (Adcon Telemetry^®, Vienna, AT) located in the study area. The calculation of degree-days (˚D) was performed using Equation (2).

˚D = (Maximum temperature + Minimum temperature)/2 − 18.6 (2)

where 18.6˚C was the base temperature [2]. Weekly observations were made for one year, and the different phenophases were identified.

A third-degree polynomial was adjusted in a variable with phenological stages based on cumulative day-degrees. The phenological stages for Jatrophaplatyphylla were defined by a decimal scale, following the methodology proposed by the Federal Biological Research Centre for Agriculture and Forestry [18].

Seed germination began on the third day after sowing and continued upon the fifth day at an average temperature of 21˚C. 80% germination was observed in the 8 genotypes. The shelled seed opened and the radicle showed a constant and vertical growth that constitutes the taproot and four lateral roots with abundant ramifications (Figure 1(a)).

The structural characteristics of roots may therefore provide soil resistance to water and wind erosion in some sites [19] [20]. J. platyphylla presented epigeal germination, where cotyledons emerged above the ground, as for most species of this genus [21]. The cotyledons are wrapped by the thick endosperm and reddish-white coloration. The verticality of the hypocotyl and the emergence of the second leaf true made evident the beginning of vegetative development, where you can see the deployment of the leaves cotyledonary, foliage development and fall of cotyledons.

The stem bark is whitish gray and was observed straight without ramifications during the first year (Figure 1(b)). The leaves are distributed alternately (spiral) along the stem and have 5 ribs principal. Each leaf is 33 to 42 cm long and 35 to 44 cm wide. The leaf is peltated because the petiole is inserted almost to the center of the leaf, the petiole is 20 to 38 cm long and has a basal diameter of 7 to 8 mm (Figure 1(c)). Dehgan [4], describes the leaves of J. platyphylla as thickened,

25 to 35 cm, peltated, it should be noted that the description does not mention the size of the petioles, it only describes them as long petioles.

The morphological and anatomical variation of the leaves of the genus Jatropha facilitate taxonomic classification. The leaf of the species of the genus varies even those with 35 to 40 cm long [22]. The leaf blades are armored with 5 lobes. They presented stomata only in abaxial epidermis (hypostomatic) and stomata are of paracytic type. (Figure 2), unlike Jatrophacurcas that presents stomata on both surfaces [23]. The stomatic index was found in a range from 23.08 to 35.14 in contrast J. curcas attain average of 7.076 in adaxial and 30.959 in abaxial surface [24]. Stomata are a promising trait as they reveal information on habitat preferences and there with ecological characteristics of species such as light conditions, as water use [25].

The pistillate and staminate flowers of J. platyphylla are white, The pedicel of the pistillate flower ranged in a range of 10.43 to 16.69 mm long (Figure 1(d)) and 4.28 to 5.49 mm for the staminate flower (Figure 1(e)), both presented 5 petals 5.14 mm wide on average and 8.29 mm long; sepals 12 to 15 mm long by 5 - 6 mm wide. Dehgan and Schutzman [26] describe the sex of the J. platyphylla plant as dioecious, however; monoecious individuals were identified that presented male and female flowers in the same inflorescence only in PP (Mocorito, Sinaloa) genotypes (Figure 1(f)).

Fruits are trilocular and tricarpelar drupe fleshy capsules that are initially green in colour, but turn yellow and then yellowish-brown and dehiscent as it matures (Figure 1(g)). In the genotypes, TP (Tamazula, Durango) and LH (La Higuerita, Sinaloa), the development of fruits with four carpels and four seeds was observed (Figure 1(h)). Its dimensions are 4.5 cm wide and 4.5 cm high, with a weight of 31 to 45 grams. The weight of the mature fruit of J. platyphylla corresponds to 15% of seeds and 75% of mesocarp and epicarp. Each fruit presented a seed in each locule, round brown in shape, with thick endocarp, weighing 1.01 to 2.06 grams, with an average weight of 1.79 ± 0.22, diameter of 13.03 to 16.02 mm (14.63 ± 0.60). These results agree with Makkar et al. [9], who describe the almost circular seed with a diameter of 15.54 ± 1.01 mm. The average weight of 1.80 ± 0.15 for the whole seed, 0.92 ± 0.01 for the shell and 0.85 ± 0.13 for the kernel. Shells represent more than 50% of the total weight of the seed. On the other hand, Standley [6] reports 12 mm seeds (Figure 1(i)). The difference in diameter may be due to the climatic and edaphological conditions in which the plants were, or to the genotypes under study [27] [28].

The development of Jatrophaplatyphylla was observed in two stages: Vegetative; which included 7 phenological events (sowing, germination, emergency, cotyledonary stage, 2nd leaf, 4th leaf and term of vegetative growth), and Reproductive (flowering, fruiting, physiological maturity, defoliation and senescence) (Figure 3). Table 2 shows the relationship between the physiological time (˚D) and the chronological time obtained, and the phenological responses recorded during

the study season. The development of the plant was evident after certain phenomena, such as the appearance of the air system, manifested by the emergence of the curved hypocotyl that occurred between the fifth and fourteenth day after planting with a requirement of 98˚D. The plant was required to accumulate a total of 2558 (˚D) and 323 calendar days, to complete its biological cycle; where, 1337˚D were for the vegetative cycle and 115 calendar days, while 1221˚D and 208 calendar days were required for the reproductive cycle. It was determined that a cumulative thermal requirement of 1035˚D is necessary for the appearance of the first four true leaves. Likewise, 303˚D were required for flowering. The thermal requirements for the formation of the first fruit cluster were 1982˚D accumulated. Moraes et al. [29] evaluated Jatrophacurcas irrigated and non irrigated systems, they found for fruit development was required 3271˚D and 2245˚D, respectively. In more favorable environmental conditions, the plants require more degree days for flowering, whereas a higher percentage of energy is expended on growth and dry matter accumulation. Potentially, there is a physiological binomial growth development, which is sometimes balanced. However, increased investment in one event deters the progress of another and vice versa. The same data distribution is not recognized for the counting of days, because this variable is less appropriate for the estimation of plant development [30].

The growth of the plant expressed in height showed to be continuous. J. platyphylla grew rapidly, in 3 months it acquired a height of 30 cm on average, similar to that reported for 12, wherein 3 months it can reach between 30 and 40 cm high [31]. The plants reached an average height of 74 cm until the beginning of fruiting, where a stalk in the growth of the stem was observed, which remained constant until reaching a maximum growth of 80 cm during the cycle April 2017 to March 2018. Jatropha plants take 5 to 7 weeks to reach the appropriate transplant height in the field [31]. The phenology of fruit species such as J. platyphylla depends largely on the environmental conditions of a particular year, which is why some interannual variability can be expected in the occurrence of phenological events [32]. Reproductive development started after 4 months of sowing, in the month of September during the rainy season. However, in tropical and humid regions it occurs almost all year [31]. The continuous flowering of the place to the production of fruits for 4 months per year, so it must be harvested 3 times during this period [33]. In November, the leaf fall began and in January, completely bare plants were observed, the plant being in a state of winter rest or dormancy.

The data analysis indicates that the highest development rate occurred at an average temperature of 29˚C, where the growth increase was 18 cm. Optimal climate conditions reported for J. platyphylla include temperatures of 29˚C - 34.0˚C and annual precipitation of 800 - 1500 mm [22]. In January 2018, the average temperature was 18˚C and low plant growth (0.6 cm) was obtained. This growth habit has been described in J. curcas at range of 18˚C [33] - 18.6˚C [34]. The value of lower basal temperatures for the development of Jatropha was estimated at 7.2˚C in total cycle stage [28]. The results show that J. platyphylla responds better to climates with high average temperatures (greater than 19˚C) than to cold temperatures, where its growth decreases (Figure 4).

The estimated model for J. platyphylla in cumulative degree-days (˚DA) was Equation (3).

Stage = −0.0041x³ + 0.7446x² − 8.6808x + 6.2448 (3)

High correlation was observed in model (R² = 0.9927). Cesaraccio et al. [35] mentioned if a model is accurate, the regression slope should be near unity and the intercept near zero. Using the fitted model it was possible to determine phenological stage record from the date of sowing the maximum and minimum temperatures, and calculate the degrees days accumulated (˚DA) (Figure 5). The calculated models allow to predict of the phenological stages of the plant, for this it is necessary to record from the date of sowing the maximum and minimum temperatures, and calculate the degrees days accumulated (˚DA). Phenological models are tools aimed at knowing and predicting the development of plants such as flowering and development of seeds [30], and an instrument for observing forest phenology at climate change [36]. The application of these models includes the estimation of the harvest times of some crops; they also allow the implementation of agronomic practices oriented to increase or decrease the development of the crop, with the management of the temperature through ventilation in a production greenhouse of plants. In the same way, it can allow the planning of other management practices with great influence on growth such as fertilization, planting time, irrigation, pest management and diseases [37]. Crop and pest models can be used concurrently to forecast watering points for the crop based on the state of phenological development and thermal requirement [38] [39]. Degree-day calculations are essentially statistical features needed for calculation. In the context of nonlinear development summation, their precise values are less critical, and they are used mostly as convenient cut points for calculation. The actual existence of such thresholds is questionable, because they are very difficult to measure owing to excessive mortality when organisms are kept at those temperatures for long periods [40]. The non-linear relationship between phenology and temperature can explain the different responses to warm climates in woody and herbaceous species [41]. Observational studies at the local scale, together with local meteorological observations, can generate suggestions for possible environmental drivers of phenology [42].