Pseudophacopteron longicaudatum (Hemiptera) induces intralaminar leaf galls on Aspidosperma tomentosum (Apocynaceae): a qualitative and quantitative structural overview.

The structural complexity of galls depends on species-specific interaction driven by the galling taxa. However, the host plant and environment stressors can impose limits on gall developmental patterns and impact the establishment of gall morphology. Herein, we employed qualitative and quantitative approaches in order to elucidate how cell divisions, elongation patterns, and tissue organization are determinant for the development of intralaminar gall morphology induced by Pseudophacopteron longicaudatum Malenovský, Burckhardt, Queiroz, Isaias & Oliveira (Hemiptera: Psylloidea: Phacopteronidae) on leaves of Aspidosperma tomentosum Mart. (Apocynaceae). In addition, we aimed to determine which anatomical process can discriminate the stages of gall development, plus, examine the histochemical and cytological profiles of the galls. The differentiated structures, mainly abaxial epidermis and spongy parenchyma, are associated with gall closure, with hyperplastic events concentrated in the young phase of the galls. Thus, epidermis and spongy parenchyma hypertrophy and are responsible for the determination of the nymphal chamber formation and gall shape. The mature galls do not differentiate into a typical nutritive cells and do not develop a histochemical gradient in their tissues. The cytological features of galls such as plastoglobules and multivesicular bodies are related to ROS scavenging mechanisms due the high oxidative stress.

Synchronism between Aspidosperma macrocarpon (Apocynaceae) resources allocation and the establishment of the gall inducer Pseudophacopteron sp. (Hemiptera: Psylloidea).

The joint interpretation of phenology and nutritional metabolism provides important data on plant tissues reactivity and the period of gall induction. A population of Aspidosperma macrocarpon (Apocynaceae) with leaf galls induced by a Pseudophacopteron sp. (Psylloidea) was studied in Goiás state, Brazil. Assuming the morphological similarity between host leaves and intralaminar galls, a gradient from non-galled leaves towards galls should be generated, establishing a morpho-physiological continuum. The phenology, infestation of galls, and the carbohydrate and nitrogen contents were monthly evaluated in 10-20 individuals, from September 2009 to September 2010. Our objective was to analyze the nutritional status and the establishment of a physiological continuum between the galls and the non-galled leaves of A. macrocarpon. The period of leaf flushing coincided with the highest levels of nitrogen allocated to the new leaves, and to the lowest levels of carbohydrates. The nutrients were previously consumed by the growing leaves, by the time of gall induction. The levels of carbohydrates were higher in galls than in non-galled leaves in time-based analyses, which indicateed their potential sink functionality. The leaves were infested in October, galls developed along the year, and gall senescence took place from March to September, together with host leaves. This first senescent leaves caused insect mortality. The higher availability of nutrients at the moment of gall induction was demonstrated and seems to be important not only for the establishment of the galling insect but also for the responsiveness of the host plant tissues.

Sink Status and Photosynthetic Rate of the Leaflet Galls Induced by Bystracoccus mataybae (Eriococcidae) on Matayba guianensis (Sapindaceae).

The galling insect Bystracoccus mataybae (Eriococcidae) induces green and intralaminar galls on leaflets of Matayba guianensis (Sapindaceae), and promotes a high oxidative stress in host plant tissues. This biotic stress is assumed by the histochemical detection of hydrogen peroxide, a reactive oxygen species (ROS), whose production alters gall physiology. Thus, we hypothesize that high levels of nutrients are accumulated during gall development in response to a local maintenance of photosynthesis and to the galling insect activity. Moreover, the maintenance of low levels of photosynthesis may guarantee O2 production and CO2 consumption, as well as may avoid hypoxia and hypercarbia in gall tissues. To access the photosynthesis performance, the distribution of chlorophyllous tissues and the photochemical and carboxylation rates in gall tissues were analyzed. In addition, histochemical tests for hydrogen peroxide and phenolic derivatives were performed to confirm the biotic stress, and set the possible sites where stress dissipation occurs. The contents of sugars and nitrogen were evaluated to quantify the gall sink. Currently, we assume that the homeostasis in gall tissues is ruptured by the oxidative stress promoted by the galling insect activity. Thus, to supply the demands of gall metabolism, the levels of water-soluble polysaccharides and starch increase in gall tissues. The low values of maximum quantum efficiency of PSII (Fv/Fm) indicate a low photosynthetic performance in gall tissues. In addition, the decrease of PSII operating efficiency, (F'm-F')/F'm, and Rfd (instantaneous fluorescence decline ratio in light, to measure tissue vitality) demonstrate that the tissues of B. mataybae galls are more susceptible to damage caused by stressors than the non-galled tissues. Thus, the high oxidative stress in gall developmental sites is dissipated not only by the accumulation of phenolic derivatives in the protoplast, but also of lignins in the walls of neoformed sclereids.