High resolution leaf spectral signature as a tool for foliar pigment estimation displaying potential for species differentiation.

Optical leaf profiles depend on foliar pigment type and content, as well as anatomical aspects and cellular ultrastructure, whose effects are shown in several species. Monocotyledon and Dicotyledon plants presenting natural pigment content variations and anatomical alterations were analyzed. Each plant species displays its own spectral signatures, which are, in turn, influenced by foliar pigment class (composition) and concentration, as well as anatomical and ultrastructural plant cell characteristics. Plants with no anthocyanin displayed increased reflectance and transmittance in the green spectral region (501-565 nm), while values decreased in the presence of anthocyanin. At wavelengths below 500 nm (350-500 nm), strong overlapping signatures of phenolics, carotenoids, chlorophylls, flavonoids and anthocyanins were observed. Using a partial least squares regression applied to 350-700 nm spectral data allowed for accurate estimations of different foliar pigment levels. In addition, a PCA and discriminant analysis were able to efficiently discriminate different species displaying spectra overlapping. The use of absorbance spectra only was able to discriminate species with 100 % confidence. Finally, a discussion on how different wavelengths are absorbed and on anatomical interference of light interaction in leaf profiles is presented.

Unveiling the osmophores of Philodendron adamantinum (Araceae) as a means to understanding interactions with pollinators.

Background and Aims: Araceae species pollinated by nocturnal Cyclocephalini beetles attract their pollinators by inflorescence scents. In Philodendron , despite the intense odour, the osmophores exhibit no definite morphological identity, making them difficult to locate. This may explain why structural studies of the scent-releasing tissue are not available so far. Methods: Several approaches were employed for locating and understanding the osmophores of Philodendron adamantinum . A sensory test allowed other analyses to be restricted to fertile and sterile stamens as odour production sites. Stamens were studied under light and electron microscopy. Dynamic headspace and gas chromatography-mass spectrometry were used to collect and analyse scents from different zones of the inflorescence. Key Results: The epidermal cells of the distal portion of fertile stamens and staminodes are papillose and, similar to the parenchyma cells of this region, have dense cytoplasm and large nuclei. In these cells, the composition of organelles is compatible with secretory activity, especially the great number of mitochondria and plastids. In this portion, lipid droplets that are consumed concomitantly with the release of odour were observed. Quantitative scent analyses revealed that the scent, with a predominance of dihydro-ß-ionone, is mainly emitted by the fertile and sterile staminate zones of the spadix. An amorphous substance in the stomata pores indicates that the components are secreted and volatilized outside of the osmophore under thermogenic heat. Conclusions: Despite the difficulty in locating osmophores in the absence of morphological identity and inefficiency of neutral red staining, the osmophores of P. adamantinum have some features expected for these structures. The results indicate a functional link between thermogenesis and volatilization of osmophore secretions to produce olfactory signals for attracting specialized beetle pollinators. These first experimental data about the precise location of osmophores in Philodendron will stimulate studies in related species that will allow future comparison and the establishment of patterns of functional morphology.

In the heat of the night--alternative pathway respiration drives thermogenesis in Philodendron bipinnatifidum.

• Philodendron bipinnatifidum inflorescences heat up to 42 °C and thermoregulate. We investigated whether they generate heat via the cytochrome oxidase pathway uncoupled by uncoupling proteins (pUCPs), or the alternative oxidase (AOX). • Contribution of AOX and pUCPs to heating in fertile (FM) and sterile (SM) male florets was determined using a combination of oxygen isotope discrimination, protein and substrate analyses. • Both FM and SM florets thermoregulated independently for up to 30 h ex planta. In both floret types, AOX contributed > 90% of respiratory flux during peak heating. The AOX protein increased fivefold with the onset of thermogenesis in both floret types, whereas pUCP remained low throughout development. These data indicate that AOX is primarily responsible for heating, despite FM and SM florets potentially using different substrates, carbohydrates or lipids, respectively. Measurements of discrimination between O2 isotopes in strongly respiring SM florets were affected by diffusion; however, this diffusional limitation was largely overcome using elevated O2. • The first in vivo respiratory flux measurements in an arum show AOX contributes the bulk of heating in P. bipinnatifidum. Fine-scale regulation of AOX activity is post-translational. We also demonstrate that elevated O2 can aid measurement of respiratory pathway fluxes in dense tissues.

Delayed leaf senescence by exogenous lyso-phosphatidylethanolamine: towards a mechanism of action.

Exogenous application of the lysophospholipid, lyso-phosphatidylethanolamine (LPE) is purported to delay leaf senescence in plants. However, lyso-phospholipids are well known to possess detergent-like activity and application of LPE to plant tissues might be expected to rather elicit a wound-like response and enhance senescence progression. Since phosphatidic acid (PA) accumulation and leaf cell death are a consequence of wounding, PA- and hormone-induced senescence was studied in leaf discs from Philodendron cordatum (Vell.) Kunth plants in the presence or absence of egg-derived 18:0-LPE and senescence progression quantified by monitoring both lipid peroxidation (as the change in malondialdehyde concentration), and by measuring retention of total chlorophyll (Chl(a+b)) and carotenoids (C(c+x)). Only abscisic acid (ABA) stimulated lipid peroxidation whereas ABA, 1-aminocyclopropane-1-carboxylic acid (ACC), the immediate precursor to ethylene (ETH), and 16:0-18:2-PA stimulated loss of chloroplast pigments. Results using primary alcohols as attenuators of the endogenous PA signal confirmed a role for PA as an intermediate in both ABA- and ETH-mediated senescence progression. Exogenous 18:0-LPE did not appear to influence senescence progression and was unable to reverse hormone-induced senescence progression. However, when supplied together with 16:0-18:2-PA at 1:1 (mol:mol), activity of phosphatidylglycerol (PG) hydrolase, chlorophyllase (E.C. 3.1.1.14), and progression of leaf senescence were negated. This apparent anti-senescence activity of exogenous 18:0-LPE was associated with induction of the pathogenesis-related protein, extracellular acid invertase (Ac INV, E.C. 3.2.1.26) suggesting that 18:0-LPE like 16:0-18:2-PA functions as an elicitor.

Respiration of thermogenic inflorescences of Philodendron melinonii: natural pattern and responses to experimental temperatures.

The patterns of temperature and respiratory changes in the protogynous inflorescences of Philodendron melinonii (Araceae) were studied in the field in French Guiana. These are the first respiratory measurements from a member of the large subgenus Philodendron, a group previously thought to lack thermoregulatory inflorescences, in contrast to thermoregulatory Philodendron species of the subgenus Meconostigma. Heating by the male and sterile male florets was strong on the first evening of anthesis when beetles are attracted and the female florets are receptive. Heat production of the inflorescence peaked at approximately 0.9 W and spadix temperature reached approximately 39.5 degrees C, a level somewhat independent of ambient temperature. Thermogenesis continued throughout the night and the next day, but at a lower level, and floral temperatures fell. On the second evening, when pollen was shed, there was a small elevation in respiration and spadix temperature. Responses of cut spadix sections to experimental step changes in ambient temperature resulted in a prompt response in floral temperature and respiration rate in the direction of the change and then a much slower regulatory adjustment in the opposite direction. These responses are consistent with an immediate van 't Hoff effect, followed by up- or down-regulation of thermogenesis. However, the responses required several hours. It is concluded that the male floret tissues possess the same thermoregulatory mechanism of more precise thermoregulatory species, but a combination of small spadix size (that favours heat loss), moderate thermogenic capacity (that limits heating rate), and slow reaction time (that causes long lags between temperature change and the regulatory response) result in poor thermoregulatory performance during the second day.

Quantitative developmental analysis of homeotic changes in the inflorescence of Philodendron (Araceae).

BACKGROUND AND AIMS: The inflorescence of Philodendron constitutes an interesting morphological model to analyse the phenomenon of homeosis quantitatively at the floral level. The specific goals of this study were (1) to characterize and quantify the range of homeotic transformation in Philodendron billietiae, and (2) to test the hypothesis that the nature of flowers surrounding atypical bisexual flowers (ABFs) channel the morphological potentialities of atypical bisexual flowers. METHODS: Inflorescences of P. billietiae at different stages of development were observed using SEM. The number of appendices in male, female and sterile flowers were counted on 11 young inflorescences (5-6 flowers per inflorescence). The number of staminodes and carpels on ABFs were counted on 19 inflorescences (n = 143). These data were used for regression and ANOVA analyses. RESULTS: There was an average of 4.1 stamens per male flower, 9.8 carpels per female flower and 6.8 staminodes per sterile male flower. There was an average of 7.3 floral appendices per atypical flower. Staminodes and carpels are inserted on the same whorl in ABFs. A negative exponential relationship was found between the average number of staminodes and the number of carpels in ABFs. If only the ABFs consisting of less than six carpels are considered, there is a linear relationship between the number of carpels and the average number of staminodes. The value of the slope of the regression equation indicates that on average, in P. billietiae, 1.36 carpels are replaced by one staminode. CONCLUSIONS: In P. billietiae, the number of appendages in female flowers imposes a constraint on the maximum total number of appendages (carpels and staminodes) that can develop on ABFs. The quantitative analyses indicate that the average number of different types of floral appendages on an ABF and the number of organs involved in a homeotic transformation are two independent phenomena.

Study of homeosis in the flower of Philodendron (araceae): a qualitative and quantitative approach.

This study deals specifically with floral organogenesis and the development of the inflorescence of Philodendron squamiferum and P. pedatum. Pistillate flowers are initiated on the lower portion of the inflorescence and staminate flowers are initiated on the distal portion. An intermediate zone consisting of sterile male flowers and atypical bisexual flowers with fused or free carpels and staminodes is also present. This zone is located between the sterile male and female floral zones. In general, the portion of bisexual flowers facing the male zone forms staminodes, and the portion facing the female zone develops an incomplete gynoecium with few carpels. The incomplete separation of some staminodes from the gynoecial portion of the whorl shows that they belong to the same whorl as the carpels. There are two levels of aberrant floral structures in Philodendron: The first one is represented by the presence of atypical bisexual flowers, which are intermediates between typical female flowers and typical sterile male flowers. The second one is the presence of intermediate structures between typical carpels and typical staminodes on a single atypical bisexual flower. The atypical bisexual flowers of P. squamiferum and P. pedatum are believed to be a case of homeosis where carpels have been replaced by sterile stamens on the same whorl. A quantitative analysis indicates that in both species, on average, one staminode replaces one carpel.