In crowns of chestnut trees the absorption of radiant energy is not homogeneous; leaves from the south (S) side are the most irradiated, but leaves from the east (E) and west (W) sides receive around 70 % and those from north (N) face less than 20 % of the S irradiation. Compared to the S leaves, those from the N side were 10 % smaller, their stomata density was 14 % smaller, and their laminae were 21 % thinner. N leaves had 0.63 g(Chl) m-2, corresponding to 93 % of total chlorophyll (Chl) amount in leaves of S side. The ratios of Chl a/b were 2.9 and 3.1 and of Chl/carotenoids (Car) 5.2 and 4.8, respectively, in N and S leaves. Net photosynthetic rate (PN) was 3.9 µmol(CO2) m-2 s-1 in S leaves, in the E, W, and N leaves 81, 77, and 38 % of that value, respectively. Morning time (10:00 h) was the period of highest PN in the whole crown, followed by 13:00 h (85 % of S) and 16:00 h with 59 %. Below 500 µmol m-2 s-1 of photosynthetic photon flux density (PPFD), N leaves produced the highest PN, while at higher PPFD, the S leaves were most active. In addition, the fruits from S side were 10 % larger than those from the N side. and J. Gomes-Laranjo ... [et al.].
The responses of rates of net photosynthesis (F^) to photosynthetic photon fluence rate (i), leaf temperature and CO2 were studied inhalf-sib families of greenhouse and field grown black locust (Robinia pseudoacacia L.) seedlings. The response of to 1 was similar in both greenhouse and field grown seedlings, except the quantum yields were lower in the field grown seedlings. The saturáting / was as low as 600 pmol m'^ s'’ in some seedlings but did not saturate at 1900 púiol m'^ s'^ in others. The optimum temperature for in field grown seedlings was shghtly lower than the greenhouse grown seedlings. increased rapidly with increased CO2 up to 350 pmol mol'^ but beyond SOO pmol mol'* the increase was gradual in some families. On average, stomata represented only 23 % of the limitation to Pii with no differences between families observed. Family x I, family x temperature and family X CO2 were not significant for Pj^.
The Henstock-Kurzweil approach, also known as the generalized Riemann approach, has been successful in giving an alternative definition to the classical Itô integral. The Riemann approach is well-known for its directness in defining integrals. In this note we will prove the Fundamental Theorem for the Henstock-Kurzweil-Itô integral, thereby providing a characterization of Henstock-Kurzweil-Itô integrable stochastic processes in terms of their primitive processes.
The ratío between carotenoid and chlorophyll a concentrations (Car/Chla) is indicative of the physiology and phenology of plants. With the aim of assessing this Car/Chla pigment ratio from reflectance (R), a wide range of leaves from several species and conditions were measured with high spectral resolution spectroradiometers for X between 400 and 800 nm. The performances of three pigment reflectance indices; (7) simple ratio pigment index (SRPI = R^*/R^2), (2) normalized difference pigment index [NDPI = (R^’ - R^^y^^RXi + R^2)]^ g^d (i) the structure insensitive pigment index [SIPI = (R**^ - R^i)/(R®*^ - R^^)] were tested. For each pigment index, every set of wavebands [Aj, X'^ was systematically tested. High correlations with Car/Chla were found for all these pigment indices in the blue-red domain [400 nm<A,i<530 nm, 600 nm<A,2<700 nm] as expected since both Chl and Car absorb in the blue, while only Chl absorbs in the red. The best semi-empirical estimation of the Car/Chla ratio was provided by SIPI for the wavelengths 445 and 680 nm: Car/Chla = 4.44 - 6.77 exp[-0.48 (R^oo. r445)/(r800 . R680)j| This index minimizes the confounding effects of leaf surface and mesophyll structure. These reflectance pigment indices provide new insight in the use of remote sensing for the assessment of physiology and phenology of vegetation.
The development of the nematode Procamalianus (Spirocamallanus) neocaballeroi (Caballero-Deloya, 1977), an intestinal parasite of the characid fish, Astyanax fasciatus (Cuvier) in Mexico, was studied in the experimental copepod intermediate host, Mesocyclops sp. After the copepod’s ingestion of free first-stage larvae of the nematode, these penetrate into the haemocoel of the intermediate host; they moult twice (on the 3rd and 4-5th day p.i. at 21-22”C) before they attain the third, infective stage. The third-stage larva already possesses the large buccal capsule subdivided into an anterior broad portion with eight spiral thickenings (as observed in lateral view) and a narrow posterior portion, and its tail tip bears three conical processes. The definitive host acquires infection by feeding on infected copepods; in the intestine of this fish, the nematode larvae undergo two more moults (on the 10th and 14-15th day p.i. at 25-32°C) before attaining their maturity. The prepatent period is approximately two months.