Gall-inducing Aphididae may feed directly on phloem, whereas Eriophyidae and Nematoda feed on cells lining the gall chambers. We assume that a variation in structural complexity will occur within galls induced by each taxon, and that the complexity of the galls could be related to the types of storage tissue they have. Histological, histometric, and histochemical analyses were used to compare six gall systems with different levels of complexity. Such levels are not taxon-related, even though eriophyid galls are usually simpler than nematode and aphid galls. The histological features of galls allowed the classification of storage tissues into three types: typical nutritive tissues (TNT), common storage tissues (CST), and nutritive-like tissues (NLT). The TNT and NLT have cells with dense cytoplasm and a prominent nucleus. The CST cells are vacuolated, and may store starch and other energy-rich molecules, as do the NLT cells. In contrast to NLT or CST, the TNT serves as a direct food source for gall inducers, and it is present in nematode and some eriophyid galls. NLTs may be present in some aphid galls, but are not the direct feeding site. The CST occurs on galls of all three inducing taxa.

SummaryPolyethylene glycol (PEG) is a low-cost and advantageous embedding medium, which maintains the majority of cell contents unaltered during the embedding process. Some hard or complex plant materials are better embedded in PEG than in other usual embedding media. However, the histochemical tests for phenolics and lignins in PEG-embedded plant tissues commonly result in false negatives. We hypothesize that these false negatives should be prevented by the use of distinct fixatives, which should avoid the bonds between PEG and phenols. Novel protocols for phenolics and flavanols detection are efficiently tested, with fixation of the samples in ferrous sulfate and formalin or in caffeine and sodium benzoate, respectively. The differentiation of lignin types is possible in safranin-stained sections observed under fluorescence. The Maule's test faultlessly distinguishes syringyl-rich from guaiacyl-and hydroxyphenyl-rich lignins in PEG-embedded material under light microscopy. Current hypothesis is corroborated, that is, the adequate fixation solves the false-negative results, and the new proposed protocols fill up some gaps on the detection of phenolics and lignins. (J Histochem Cytochem 65:105-116, 2017)

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