Wheat chromosome 2D carries genes controlling the activity of two DNA-degrading enzymes

DNA-degrading enzymes of 24.0 kDa and 27.0 kDa were observed to have different activities in two common wheat (Triticum aestivum L.) cultivars, Wichita and Cheyenne. A substrate-based SDS-PAGE assay revealed that these two enzymes were much more active in Wichita than in Cheyenne. Genes controlling the activities of these two enzymes were localized on chromosome 2D by testing DNA-degrading activities in reciprocal chromosome substitution lines between Wichita and Cheyenne. While the allele on Wichita chromosome 2D stimulated the activities of the 24.0- and 27.0-kDa enzymes in Cheyenne, the allele on Cheyenne chromosome 2D did not reduce the activities of the 24-kDa and 27-kDa enzymes in Wichita. Whether these genes code for the DNA-degrading enzymes themselves or for factors that regulate the enzyme activities remains unknown.This work was supported in part by USDA-Competitive Research Grants Office grant No. 90-37140-5426 to P.S.B. Contribution from Agricultural Research Division, University of Nebraska. Journal Series Number 10304     

Der eilegeapparat der odonaten

Zusammenfassung Der Eilegeapparat mit drei Paar Gonapophysen wind als der ursprünglichste angesehen und vollständiger Eilegeapparat genannt; alle Typen mit weniger als drei Gonapophysenpaaren sind von ihm durch Rudimentation abzuleiten und werden als unvollständiger Eilegeapparat zusammengefaßt.Am vollstandigen Eilegeapparat sind seine Teile durch Gelenke und Muskeln beweglich, am unvollstandigen sind sie starr ; Gelenke und Legemuskeln fehlen. Die fur die Eiablage wichtigen Gelenke und Muskeln werden beschrieben.Die Entwicklung des vollstandigen Eilegeapparates erfolgt bei der Larve in der Reihenfolge, daß zuerst die Gon. laterales, hierauf die mediales und zuletzt die anteriores ausgebildet werden. Die Rudimentation des unvollstandigen geschieht in der gleichen Reihenfolge, indem zuerst die Gon. laterales und als letzte die anteriores zurück-gebildet worden.Die Eiablage erfolgt beim vollstandigen Eilegeapparat primär exophytisch durch Ablage auf dem Boden oder endophytisch durch Einstechen in Pflanzengewebe, beim unvollstandigen Eilegeapparat exophytisch durch Ablage in das Wasser.Es wind angenommen, daß die primär exophytische Ablageart die ursprünglichste ist und alle anderen von ihr abzuleiten sind.Die endophytische Ablage entwickelt an den Gonapophysen verschiedene Anpassungen, die exophytische führt zu ihrer Rudimentation.Anpassungen an die endophytische Ablage sind Verkürzung der Gonapophysen, Entwicklung eines Tastapparates (Styli), eines Schneide-apparate (Gon. mediales), einer Legeröhre (Gon. anteriores) und einer Stützkante an den Gon. laterales, Ablage in Gonaphysenstellung, oder am 10. Sternit, Ablage in Sternitstellung.Ablage in Gonapophysenstellung beansprucht die Gon. laterales und führt bei Ablage in ein Substrat von zunehmender Härte - sie erfolgt in extremen Fallen in Baumstämme — zu verschiedenen Modifikationen ; Ablage in Sternitstellung läßt die Gon. laterales unbeansprucht und könnte bei Ablage in ein Substrat von abnehmender Härte — sie erfolgt in extremen Fallen in Schlamm — zu Rudimentation der Gon. laterales und exophytischer Ablage in das Wasser überleiten.Der unvollständige Eilegeapparat zeigt eine große Formenmannigfaltigkeit, die sich aber auf zwei Grundtypen, einem mit zwei Paar Gonapophysen — es fehlen die Gon. laterales — und einem mit einem Gonapophysenpaar, der Scheidenklappe, einem Rudiment der Gon. anteriores, zurückführen lassen.Der Zweigonapophysentypus ist bei verschiedenen Gruppen erhalten; bei den Cordulegasterinae ist er morphologisch einheitlich, was einen Stillstand des Rudimentationsprozesses andeutet, und an eine bestimmte Eiablageart angepaßt; bei den anderen Gruppen ist er morphologisch sehr verschieden, wobei es sich wohl um verschiedene Rudimentationsstufen handelt, und fur die Eiablage funktionslos geworden.Der Scheidenklappentypus findet sich bei den Gomphidae, Corduliidae und Libellulidae. Ursprünglichere Formen zeigen längere, höher entwickelte, kürzere Scheidenklappen. Bei vielen Arten ist die Scheidenk1appe restlos rudimentiert. Ihre Rolle für die Eiablage ist fraglich, vielleicht nur sinnesphysiologischer Art. Mechanisch zu deutende Formen (Spitzhammerbildung) kommen vor und sind gelegentlich mit Eiablage auf dem Boden verbunden, was als Anklänge an eine primär exophytische Ablage gedeutet wird.Bei den Libellulidae werden vereinzelt sekundäre Apparate aus neuen Elementen entwickelt.Die Eizahl ist bei Formen mit vollständigem Eilegeapparat höher als bei Formen mit ,unvollständigem und bei den Corduliidae und Libellulidae am höchsten.Die morphologische Vielfalt der Eilegeapparate ist das Ergebnis von zwei Verhaltensänderungen, dem Üborgang der Imagines zu einer Ablage durch Einstechen in Pflanzengewebe und dem Übergang der Larven zum Leben im Wasser. Diese Änderungen wurden von den einzelnen Gruppen auf verschiedene Weise und in verschiedenem Ausmaße vollzogen und ließen eine Unzahl von morphologischen Typen entstehen.Das Bestreben, die Eier möglichst nahe dem Wasser abzulegen, führte jene Gruppen, die nicht oder nicht zu weit an die Ablage in Pflanzengewebe angepaßt waren, zur Ablage in das Wasser. Diese Ab lageart führte zur Rudimentation der Gonapophysen und ließ möglicherweise neue, der neuen Ablageart angepaßte Apparate entstehen.Die Rudimentation der Gonapophysen ermöglichte eine Erhöhung der Eizahl und führte these Gruppen zur Besiedlung von neuen Lebensräumen und damit zu ihrer heute dominierenden Stellung innerhalb der Ordnung.     

α-Gustducin immunoreactivity in the airways

The G-protein subunit -gustducin is a marker of chemoreceptive cells. In the present study, we examined the immunohistochemical localization of -gustducin in rat airway epithelium both by light and electron microscopy. -Gustducin immunoreactivity was found in solitary cells that presented ultrastructural features of chemoreceptor cells, i.e. flask-shaped or pear-shaped, with an apical process with thin microvilli protruding into the lumen. The immunostaining was mainly concentrated in the apical process and along the basolateral cell surface. To investigate whether -gustducin-immunoreactive cells represented a distinct cell subset in rat airways, we performed double-label immunocytochemistry with antibodies to protein gene groduct (PGP) 9.5, a marker of neuroendocrine cells, and to phospholipase C beta2 (PLC2), a component of the bitter signalling pathway. -Gustducin-immunoreactive cells were present in a subset of PGP-9.5-immunoreactive elements, although not all -gustducin-positive cells expressed PGP 9.5 labelling. In addition, a subset of -gustducin-expressing cells colocalized PLC2. This work thus demonstrates that solitary -gustducin-immunoreactive cells exist throughout the airways and represent a specialized cell type with morphological and immunohistochemical characteristics of chemoreceptor cells.     

Effect of nitrogen on thiocyanate content of Brassica oleracea var. acephala leaves

An experiment was carried out to study the effect of nitrogen fertilizer application levels (0, 47, 94 and 188 kg N/ha) on thiocyanate contents of petioles and lamina of two Brassica oleracea L. var. acephala varieties (Thousand-headed kale and Georgia collards).The results showed that N application significantly decreased thiocyanate contents of both laminae and petioles. Applying 47, 94, 188 kg N/ha reduced thiocyanate of laminae and petioles by 26, 41 and 52% and 2, 9 and 39%, respectively. The results also showed that thiocyanate of leaves from Thousand-headed kale was significantly higher than that of Georgia collards. Lamina and petiole thiocyanates of Georgia collards were 79% and 83% of those of Thousand-headed kale, respectively.     

Histochemical studies of dehydrogenases in the developing teeth

Summary Histochemical observations were made of oxidative and reducing enzymes in relation to several metabolic pathways in the developing tooth. The localization and activity of dehydrogenases and oxidases could be divided roughly into two types.Type one refers to enzymatic activities of lactic, succinic, malic and glucose-6-phosphate dehydrogenase and aconitase and cytochrome oxidase, which were low in undifferentiated dental epithelium and increased in proportion to cell differentiation. Comparatively high enzymatic activities were reflected in high cell function.Type two did not increase in the enzymatic activity during differentiation. Glyceraldehyde-3-phosphate, TPN isocitric, 6-phosphogluconate, glutamic, -glycerophosphate and -hydroxybutyric dehydrogenase and monoamine oxidase belong to this type.With 12 Figures in the TextPresented in Parts at the 3rd Annual Meeting in September, 1962 of the Japanese Histochemical Association.     

Current chemical concepts of acids and bases and their application to anionic (“acid”) and cationic (“basic”) dyes

Summary In biomedical studies, dyes are divided into acid and basic dyes. This classification cannot be reconciled with current chemical definitions of acids and bases. Brönsted-Lowry acids are compounds that can donate protons; bases are proton acceptors. The definition of acids and bases is independent of the electric charge, i.e. acids and bases can be neutral, anionic or cationic. Reactions between acids and bases result in formation of new acid-base pairs. Lewis acids and bases do not depend on a particular element, but are characterized by their electronic configurations. Lewis bases are electron donors; Lewis acids are electron acceptors. This classification is also unrelated to the electric charge. Lewis acids and bases interact by formation of coordinate covalent bonds.In histochemistry and histology, dyes containing SO ₃ ^– , –COO^– and/or –O^– groups are classified as acid dyes. However, such compounds are electron pair donors and hence Brönsted-Lowry and Lewis anionic bases. Dyes carrying a positive charge are termed basic dyes. Chemically, many cationic dyes are Lewis acids because they can add a base, e.g. OH^–, acetate, halides. The hypothesis that transformation of –NH₂ into ammonium groups imparts basic properties to dyes is untenable; ammonium groups are proton donors and hence acids. Furthermore, conversion of an amino into an ammonium group blocks a lone electron pair and the color of the dye changes drastically, e.g. from violet to green and yellow. It appears therefore highly unlikely that ammonium groups are responsible for binding of cationic (basic) dyes. In histochemistry, it is usually not of critical importance whether anionic or cationic dyes are chemically acids or bases. It is therefore suggested to substitute the terms anionic for acid and cationic for basic dyes; this nomenclature will always be chemically correct.     

Effects of 17β-estradiol on the distribution and activity of some oxydative enzymes of uterine and cervical epithelium in neonatal mice

Summary The following enzymes were studied histochemically in uterine and cervical epithelium from neonatal mice treated with 17-estradiol for the first four days after birth: NADH-, NADPH-, succinate-, -glycerophosphate-, lactate-, glucose-6-phosphate-, and 17-OH-steroid dehydrogenases.It was demonstrated that estradiol administration had a marked influence on distribution and activity of several of the enzymes compared with the control animals. In cervix there was an increase of activity for most of the enzymes, especially in the apical parts of the epithelium cells. The uterine epithelium was also estradiol sensitive as regards most enzymes, and in the case of glucose-6-phosphate dehydrogenase there was a dramatic enhancement of reaction in the uterus of the experimental animals. The differences obtained between cervical and uterine epithelium are described.17-OH-steroid dehydrogenase could not be detected histochemically in the present material.Supported by the Norwegian Research Council for Science and the Humanities.     

Structure of tanacetan,a pectic polysaccharide from tansy Tanacetum vulgare L

Tanacetan TVF was found to have a branched structure with a backbone of linear -1,4-D-galacturonan. The ramified regions consist of linear -1,2-L-rhamno--1,4-D-galacturonan as the core. The side chains appear to attach to the 4-position of the L-rhamnopyranose residues. They are present as single -galactopyranose residues or a branching -1,4-galactopyranan bearing 4,6-substituted -D-galactopyranose residues as branched points. In addition, the ramified regions contain side chains of a branched -1,5-arabinofuranan possessing 2,5- and 3,5-substituted -L-arabinofuranose residues as branching points. Some side chains of rhamnogalacturonan appear to be arabinogalactan which contains branched sugar chains of -1,5-arabinofuranan attached to the linear chains of -1,4-galactopyranan by 1,3- and 1,6-linkages. The residues of -L-arabinofuranose seem to occupy the terminal positions of the arabinogalactan side chains.     

Influence of Antiviral Factor on Tobacco Mosaic Virus RNA Biosynthesis in Tobacco

An antiviral factor (AVF) was separated by removing virus particles from extracts of tobacco mosaic virus (TMV) infected leaves using calcium phosphate gel and by column chromatography on DEAE cellulose. AVF was not found in the extracts from healthy plants. The AVF restricted the virus infectivity in vivo and significantly decreased the activity of key enzymes of metabolic pathways tending to the purine and pyrimidine nucleotides biosynthesis of viral- RNA (glucose-6-phosphate dehydrogenase, ribonucleases, phosphomonoesterase and phosphodiesterase). No inhibition of these enzymes was observed in vitro when the effect of different concentrations of AVF (0.25 – 250 µg cm^–3) was examined.     

The ultrastructural localization of the enzymes related to steroid hormone metabolism in the guinea-pig testis

Synopsis A study of the ultrastructural localization of 3-hydroxysteroid dehydrogenase (3-HSD), 11-hydroxysteroid dehydrogenase (11-HSD), glucose-6-phosphate dehydrogenase (G-6-PD), -hydroxybutyrate dehydrogenase (-HBD), NADH diaphorase (NADH-D) and NADPH diaphorase (NADPH-D) in the guinea-pig testis is reported.The procedures employed included short immersion or perfusion fixation with aldehydes followed by incubation of small blocks in a tetrazolium salt or a ferricyanide medium. The effects of incubation conditions were investigated, and a reaction medium for the ultracytochemical demonstration of 11-HSD is described. Using suitable controls, evidence for the specificity of the cytochemical reactions is presented.It was found that all the enzymes studied were present in both the Leydig and Sertoli cells of the guinea-pig testis and that the intracellular distribution pattern for each enzyme was independent of the cell type. Using tetrazolium salt techniques, both 3-HSD and 11-HSD activities were localized on or in membranes of smooth endoplasmic reticulum and within the mitochondria. With the ferricyanide techniques, G-6-PD activity was found to be associated mainly with the smooth endoplasmic reticulum membranes, while -HBD activity was limited to mitochondria. With both the tetrazolium salt and ferricyanide techniques, the reaction products for NADH-D and NADPH-D activities showed localizations which were similar to those observed for the steroid dehydrogenases.     

Evidence for the deficiency of β-glucosidase-activating factor in fibroblasts of patients with I-cell disease

Summary Reduced activity of -glucosidase was shown in the cultured skin fibroblasts of four patients with I-cell disease when the enzyme was tested without the use of detergents. In the presence of taurocholate and triton X100 -glucosidase activity was normal. This suggested a deficiency of a -glucosidase-activating factor in I-cell fibroblasts rather than of the enzyme itself. The deficiency of -glucosidase activity was corrected to some extent by mixing cell lysates, and more effectively by cocultivation and fusion of I-cell disease and Gaucher fibroblasts. These results present evidence for the presence of a -glucosidase-activating factor in normal and Gaucher fibroblasts. In fibroblasts of patients with I-cell disease this activator is probably deficient, as is the case for most lysosomal enzymes.     

Selective amidation of carboxyl groups of the intermolecular contact regions of hemoglobin S: Structural aspects

Carboxyl groups of HbS are readily activated by water-soluble carbodiimide atpH 6.0 and room temperature. These o-acylurea intermediates (activated carboxyl) are accessible for nucleophilic attack by amines. With glycine ethyl ester, the amidation is very selective for the -carboxyl of Glu-43() and more than 65% of the glycine ethyl ester incorporated is on this carboxyl group. In contrast, glucosamine derivatizes the -carboxyl group of Glu-22() as well as that of Glu-43() to nearly the same degree. However, the total amidation of HbS by glucosamine is lower than that with glycine ethyl ester. The differential selectivity of the two amines is apparently related to the differences in the microenvironment of the -carboxyl groups of Glu-22() and Glu-43(), which either facilitates or refracts the aminolysis of the activated carboxyl with the two amines to different degrees. The carboxyl groups of isolated -chain exhibit a higher reactivity for amidation with glycine ethyl ester than does the tetramer. The carboxyl groups of Glu-22() and Glu-43() and that of Asp-47() are all activated by carbodiimide suggesting that the higherpK_a of these carboxyl groups (facilitating the activation) is a property of tertiary interaction of the polypeptide chain. The interaction of the -chain with -chain, i.e., generation of the quaternary interactions, reduces overall reactivity of the carboxyl groups of the protein. The higher selectivity of hemoglobin S for amidation at Glu-43() with glycine ethyl ester compared with that of isolated -chain appears to be primarily a consequence of decreased amidation at sites other than at Glu-43().     

Soil and xylem water potential and soil water content in contrasting Pinus contorta ecosystems,Southeastern Wyoming,USA

Summary The relationships between volumetric soil water content (), in situ soil water potential (_soil) and predawn xylem pressure potential (_predawn) were quantified in four contrasting lodgepole pine ecosystems in Wyoming, USA. On three of the sites, changes in _soil correlated closely with _predawn, but on a porous soil derived from coarse granitic parent material, _predawn declines occurred much sooner than corresponding declines in _soil, possibly because of local depletion of rhizosphere moisture and low molecular diffusivity of water in that soil. Exptrapolation of laboratory-derived characteristic curves for soil moisture to field conditions yielded different relationships between and _soil than curves derived from in situ measurements, probably because of disruption of soil structure and porosity during sample collection and handling in laboratory studies. Although a close correlation between and _predawn was observed, future efforts at modelling the soil-plant-atmosphere continuum should be directed towards a more detailed understanding of the complex relationships between _soil at varying depths and plant water stress.     

Further enzyme histochemical observations on the segmentation of the proximal tubules in the kidney of the male rat

Summary The segmentation of the proximal tubules of the male rat kidney was studied by means of enzyme histochemical reactions. Soluble oxidoreductases (glucose 6-phosphate dehydrogenase, -glycerophosphate dehydrogenase, 3-hydroxysteroid dehydrogenase, NAD- and NADP-dependent isocitrate dehydrogenases, NAD-dependent malate dehydrogenase, NADP-dependent, decarboxylating malate dehydrogenase, uridine diphosphate glucose dehydrogenase) were demonstrated using methods which reduce enzyme diffusion (incubating in presence of polyvinyl alcohol) and eliminate interference from tissue tetrazolium reductases. Less soluble or insoluble enzymes (glucose 6-phosphatase, -hydroxybutyrate dehydrogenase, succinate dehydrogenase and tetrazolium reductases) were demonstrated by incubation in conventional watery media.Segmental differences were observed in respect to all enzymes studied, and most reactions clearly visualized the three segments known to exist from ultrastructural as well as previous histochemical studies: The pars convoluta includes the first (P₁) and most of the second (P₂) segment. The transition to the third segment (P₃) is in the beginning of the pars recta. Also these reactions revealed a difference between the first part of the P₃, which runs through the cortex in the medullary rays, and the terminal part transversing the outer stripe of the medulla. In most instances intensity of reaction decreased in the last portion of the P₃.A number of the enzymes studied were mainly or solely localized to the P₃ (glucose 6-phosphate dehydrogenase, -glycerophosphate dehydrogenases, -hydroxybutyrate dehydrogenase, 3-hydroxysteroid dehydrogenase, decarboxylating malate dehydrogenase and uridine diphosphate glucose dehydrogenase). Some possible functional implications of the findings are discussed.Supported by grants from Fonden til Lægevidenskabens Fremme and the Danish Medical Research Council. — Mr. Kaj L. Pedersen is thanked for valuable photographic assistance.     

Osteogenesis imperfecta type IV: evidence of abnormal triple helical structure of type I collagen

Summary Skin fibroblasts from a patient with mild osteogenesis imperfecta (OI) type IV synthesize two populations of type I procollagen molecules. One population contains pro1(I) and pro2(I) chains that migrate normally in sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-PAGE) and a second population contains only slower migrating pro1(I) and pro2(I) chains. The total amount of type I procollagen made by OI cells and the ratio of pro1(I): pro2(I) is normal. When labeled under conditions that inhibit post-translational modification of pro chains, the OI cells produce only single populations of pro1(I) and pro2(I) chains indicating that the apparent increased molecular weight of some OI pro chains is due to excessive post-translational modification rather than peptidyl insertions. Peptide maps indicate that excessive post-translational modification occurs along the entire triple helical segment of some 1(I) and 2(I) chains produced by OI cells. The effect of the mutation is to lower the melting temperature of the molecules containing slow migrating 1(I) and 2(I) chains to 39.5°C (compared to 41.5°C for control), and to delay secretion of the overmodified type I procollagen from OI cells. These data are consistent with a mutation near the carboxyl-terminal end of the triple helical domain which delays triple helical formation and renders all chains available for further post-translational modification amino-terminal to the mutation. Such alterations in triple helical structure, thermal stability, and secretion previously associated only with the lethal OI type II phenotype are thus also seen in the mild OI type IV phenotype.     

Production of thermostable amylolytic enzymes by Thermococcus hydrothermalis

A cell extract of Thermococcus hydrothermalis, grown for 6 h, gave -glucosidase activity at 14.9 U/l, degrading oligosaccharides and maltose. -Amylase, -glucosidase and pullulanase activities were detected at 289 U/l, 13.5 U/l and 30 U/l respectively in the culture medium after 24 h growth of the archaeum. All of three enzymes, characterised by a half-life time of 1 to 5 h at 95°C, degraded both the (14) and (16) linkages of polysaccharides and the (14) linkages of oligosaccharides. © Rapid Science Ltd. 1998     

A comparative study of enzyme activity variation between α-glycerophosphate and alcoholdehydrogenases in Drosophila melanogaster

An intraspecific comparison of -glycerophosphate (-GPDH: E.C.1.1.1.8) and alcohol dehydrogenase (ADH: E.C.1.1.1.1) enzyme activity levels was carried out in Drosophila melanogaster. The results indicate that (1) -GPDH is a relatively conservative and ADH a relatively variable enzyme system with regard to structurally determined activity variation but that (2) the conservative nature of -GPDH activity variation does not extend to the intra-genotypic level. The results are consistent with the view that different kinds of selective pressures are being exerted on the enzyme's structural and modifier gene loci.     

Evolution of parallel β/α-barrel enzyme family lightened by structural data on starch-processing enzymes

The parallel /-barrel domain consisting of eight parallel -sheets surrounded by eight -helices has been currently identified in crystal structures of more than 20 enzymes. This type of protein folding motif makes it possible to catalyze various biochemical reactions on a variety of substrates (i.e., it seems to be robust enough so that different enzymatic functionalities could be designed on it). In spite of many efforts aimed at elucidation of evolutionary history of the present-day /-barrels, a challenging question remains unanswered: How has the parallel /-barrel fold arisen? Although the complete sequence comparison of all /-barrel amino acid sequences is not yet available, several sequence similarities have been revealed by using the highly conserved regions of -amylase as structural templates. Since many starch-processing enzymes adopt the parallel /-barrel structure these enzymes might be useful in the search for evolutionary relationships of the whole parallel eight-folded /-barrel enzyme family.     

Improvement of β-amylase thermostability in transgenic barley seeds and transgene stability in progeny

The genetic improvement of enzymes important in the brewing process is one of the main goals of barley biotechnology. For the improvement of -amylase thermostability in barley seeds, we have already constructed a mutant thermostable -amylase gene, using site-directed mutagenesis and random mutagenesis to achieve the substitution of seven amino acids of the original barley -amylase. This sevenfold-mutant barley -amylase showed a thermostability increased by 11.6 °C compared to the original enzyme. In the present article, a thermostable -amylase gene under the control of the barley -amylase promoter was introduced to barley protoplasts, and fertile plants were generated from 9 independent transgenic lines. Subsequent analyses indicated that the thermostable -amylase gene was expressed and -amylase activity derived from both native and modified genes was detected in the seeds of 6 transgenic lines. The transgene was stably transmitted to progeny, and thermostable -amylase was synthesized in T₄ seeds, demonstrating that our strategy is applicable for the improvement of seed quality for industrial utilization.     

The probability of interspecific competitive situations in scale-insects (Homoptera,Coccoidae)

Summary A large scale survey, covering some 25 million km² of Eastern-Europe, provided distributional data, and a more detailed picture on factors determining species composition and abundance of scale-insects colonizing deciduous orchard trees. No interspecific competition or competitive situations were detected among the 21 scale insect species, when taking into consideration the whole geographic area surveyed. Of all cases, 3.2% showed significant spatial separation in smaller geographic regions. However, no evidence for competition was found between species with overlapping distributions. In the case of introduced species, the role of past competition can also be excluded. Separation was thought to be determined by differences in ecological requirements. There is some probability of competition in the transitional zone (significant separation in 0.8% of cases), and somewhat more (2.4%) in the Southern zone. There was potential competition between species classified as Mediterranean and invader subguilds (7.1% of frequent species pairs), as well as between the Southern and invader (2.4% of frequent species pairs) subguilds. Its probability was very low between the species of the endemic (0.8% of frequent species pairs) and invader (1.6% of frequent species pairs) subguilds.