Comparative morphology of the head of selected sporophagous and non‐sporophagous aleocharinae (Coleoptera: Staphylinidae): Musculature and hypopharynx‐prementum complex

To investigate whether specialization to spore‐ (or pollen‐) feeding in advanced Aleocharinae is mirrored by their head anatomy, we compiled and compared synchrotron X‐ray micro‐tomography datasets for 11 Aleocharinae in conjunction with previous data for two aleocharine and six outgroup species (two nonstaphylinids, four staphylinids). We describe the presence/absence of head muscles and investigate the variability of points of origin by character mapping analyses. Monophyly of Aleocharinae is supported by the absence of M. 48 (M. tentoriobuccalis anterior), and by changes in the origins of Mm. 1, 2, 17, 18, 28, 29, 30. Within Aleocharinae the origins of the labial muscles (Mm. 28–30) have shifted posteriorly to the gula, which might enhance the movement posterad of the hypopharynx and partly compensate for the loss of M. 48. We also analyzed the general organization of the hypopharynx‐prementum complex and the fine structure of the mandibles through SEM studies. In the absence of grinding mandibular molae like those of most mycophagous Coleoptera, seven aleocharine species studied have evolved “pseudomolae” at the ventral side of the mandibles that replace true molae as secondary grinding surfaces. In these species, the hypopharynx is elevated and displaced anteriorly, bearing a bowl‐like depression on its surface that functions as a mortar where spores are ground between the hypopharynx and the mandibles. Two of these species are not yet known to feed on spores or pollen. Another species (Oxypoda alternans) is thought to feed on fungus material but bears no pseudomolae on its mandibles. J. Morphol. 271:910–931, 2010. © 2010 Wiley‐Liss, Inc.     

Developmental changes in the structure and function of mouthparts of phyllosoma larvae of the packhorse lobster, Jasus verreauxi (Decapoda: Palinuridae)

Mouthpart morphology and feeding behaviour of Jasus verreauxi phyllosomas (instars 1-13) were examined using scanning electron microscopy and video analysis, respectively, to better understand ingestion and processing mechanisms and to identify developmental changes in feeding biology. The density, robustness and complexity of mouthpart setation increased with development, oral field increased and there were a greater number of spinose projections on maxillae 1 in mid and late instar phyllosomas. The second and third maxillipeds were able to sweep a larger area due to their increased length, which effectively increased the size of the oral field. Changes in feeding behaviour were consistent with these morphological differences between instars. In late instars, the shredding and tearing efficiency of maxillae 1 increased, larger pieces of prey were pushed between the mandibles, and the mandibles were able to effectively grind food due to a slight rotation away from the transverse plane. Both morphological and behavioural observations suggests that the absolute size range of prey increases with phyllosoma body size and the prey processing (i.e. ability to capture, manipulate and grind prey) becomes more efficient with development. We suggest early instar phyllosoma are most suited to a diet comprising softer prey items, whereas later-instar phyllosoma are better equipped to deal with larger, fleshier prey.     

The larval head of Exechia (Mycetophilidae) and Bibio (Bibionidae) (Diptera)

Exechia and Bibio have retained several plesiomorphic groundplan features of Diptera and Bibionomorpha, including a fully exposed and sclerotized head capsule, the transverse undivided labrum, the absence of movable premandibles, and undivided mandibles without combs. The fusion of the hypostomal bridge with the head capsule and largely reduced antennae are derived features shared by both taxa. The absence of teeth at the anterior hypostomal margin is a potential autapomorphy of Bibionomorpha. A basal position of Anisopodidae is suggested by a number of plesiomorphies retained in this family. Apomorphies of Bibionomorpha excluding Anisopodidae are the reduction of tentorial elements, the partial fusion of the labrum and clypeus, one-segmented antennae, the absence of a separate submental sclerite, the loss of the labial palpus, and the reduction of the pharyngeal filter apparatus. Head structures of Bibio are largely unmodified. The subprognathous orientation is one of few autapomorphic features. In contrast, the mouthparts of Exechia are highly modified in correlation with the specialized food uptake. The rasping counterrotating movements of maxillae and mandibles with teeth oriented in opposite directions are carried out by strongly developed extensors and flexors of the paired mouthparts. The modified labium mechanically supports the “drill head” formed by the mandibles und maxillae. The necessary stability of the head capsule is provided by the hypostomal bridge which also compensates the far-reaching reduction of the tentorium.     

An analysis of chewed food particle size and its relationship to molar structure in the primatesCheirogaleus medius andGalago senegalensis and the insectivoranTupaia glis

The chewed food particle size and shearing capacity of the lower molars of two primate species, the fat-tailed dwarf lemur,Cheirogaleus medius and the bushbabyGalago senegalensis, and an insectivoran, the tree shrew,Tupaia glis, were compared. Differences in the shearing design of the lower molars correlate strongly with the chewed food particle size in these species: the greater the shearing capacity, the smaller the chewed food particles. These three species are of comparable size but differ greatly in diet in the wild.C. medius primarily eats fruit and nectar, whileG. senegalensis andT. glis are largely insect-eaters. The lower molars ofG. senegalensis andT. glis show a much greater shearing capacity than do those ofC. medius. The average length of chewed food particles ofC. medius is significantly larger than that ofG. senegalensis, while that ofT. glis is intermediate between the two primates but is closer to that ofG. senegalensis. Our findings that insect-eating species grind their food more finely than do fruit- and resin-eating species can be correlated with digestibility of foods: finely chewing foods such as fruits which are low in relatively undigestible cell wall components would not greatly improve their digestibility, so a highly efficient food processing apparatus would be less important to the animal's survival. Insect-eaters much more finely chew their foods, implying that there is some constituent of insect bodies difficult to digest, and that grinding increases its digestibility. We suggest that this constituent is chitin.     

Development and metamorphosis of the feeding apparatus of the stone crab,Menippe mercenaria (brachyura,xanthidae)

Analysis of the feeding apparatus of the stone crab, Menippe mercenaria (Brachyura, Xanthidae), has demonstrated that substantial internal and external morphological alterations occur at metamorphosis and suggests that the mastication of food shifts from the mandibles to the gastric mill at that time. These changes correspond to the changes in environment and diet that take place at metamorphosis, when the previously planktotrophic larvae begin benthic life. A detailed account of the structure and development of the mandibles is presented. The mandibles of all zoeal stages are similar: The incisor process has a series of teeth and denticles and the prominent molar process appears to be well adapted for grinding food. Megalopal mandibles are transitional but have the form that is typical of all subsequent stages: The expanded incisor process is rounded and toothless and the molar process is less prominent and has lost its grinding denticles. The cardiac stomach of the zoeal stages has no gastric mill; the medial and lateral teeth of the mill first appear in the megalopa. A very simple procedure is described for preparing larval mandibles for scanning electron microscopy using the molted exoskeletons from larval rearing experiments.     

Phylogenetic relationships and the larval head of the lower Cyclorrhapha (Diptera)

We examined final‐stage larvae of all currently recognized lower cyclorrhaphan (= Aschiza) families, except Ironomyiidae and Sciadoceridae, and those of the higher cyclorrhaphan (= Schizophora) families Calliphoridae, Conopidae, Lonchaeidae, Muscidae, and Ulidiidae, and compared them with larvae of two out‐group families, Rhagionidae and Dolichopodidae, paying particular attention to structures of the head. A set of 86 morphological characters were analysed phylogenetically. The results show that the lower Cyclorrhapha is paraphyletic in relation to the higher Cyclorrhapha. The monophyly of the Cyclorrhapha is strongly supported. The lower Cyclorrhapha is resolved into two clades, based on the Lonchopteridae. Within the Syrphidae the traditional three‐subfamily system is supported, based on the Microdontinae. Within the lower Cyclorrhapha, the larval head is variable in form and arrangement of components. In Lonchopteridae, the mouth lies at the back of an open trough or furrow, comprising ventrally an elongate labium and laterally the maxilla. This arrangement of components appears to facilitate scooping food in water films. In Platypezoidea there is no furrow, and the dorsolateral lobes bearing the antennae are connected by a dorsal extension of the pseudocephalon. The main food‐gathering structure is the hooked apex of the labium, but in Phoridae the mandibles may also be important. In Eumuscomorpha the mandibles are at the apex of the head skeleton. The pseudocephalon is extended and infolded dorsally to form an oral pocket over the mouth. In the Pipunculidae, and the Microdontinae and Syrphinae of the Syrphidae, ventrally it forms a V‐shaped groove or guide along which the mandibles project. The labium is sclerotized apically, and forms a plate or tapered projection. This arrangement of components facilitates holding, piercing and extracting prey tissues. In Eristalinae the pseudocephalon is attached to the mandibles and is formed into a pair of cirri bearing mandibular lobes that lie either side of the mouth. Furthermore, the epipharynx is produced anteriorly in relation to the hypopharynx, and the labium is attached to the anterior part of the epipharynx to form a cavity or atrium. This arrangement is suited to fragmenting and imbibing solid food in Eristalinae with hooked mandibles, and when the mandibles are reduced and the mandibular lobes are inverted and sclerotized, these structures form a filter for separating fluid‐suspended particulate food. In higher Cyclorrhapha an atrium is present as in Eristalinae, but a connection between the pseudocephalon and the mandibles is absent. Instead, the pseudocephalon is bifurcate dorsally and forms a pair of cephalic lobes that ventrally ensheath each mandible. The surface of the sheath may be coated in cirri and other food‐gathering structures. The cephalic lobes, mandibular sheaths and the head skeleton are maneuverable and retractile to a higher degree than in lower Cyclorrhapha. This arrangement of components facilitates feeding on both solid food, in which the mouthooks may extend from the sheath to break the food up, and particulate and suspended food, in which the food‐gathering structures of the sheath scoop up the food. In many higher Cyclorrhapha, maneuverability is enhanced by a break between the labium and the basal sclerite, to which it is fused in all lower Cyclorrhapha. Intermediate characters and states for the structures of the higher cyclorrhaphan larval head are present in out‐groups, and lower Cyclorrhapha and homologies are discussed. Liquidity of the food is an important factor explaining the structure of the larval head in Cyclorrhapha. © 2008 The Linnean Society of London, Zoological Journal of the Linnean Society, 2008, 153 , 287–323.     

Taxonomic and functional implications of mandibular scaling in early hominins

Body mass estimates for fossil hominin taxa can be obtained from suitable postcranial and cranial variables. However, the nature of the taphonomic processes that winnow the mammalian fossil record are such that these data are usually only available for the minority of the specimens that comprise the hypodigm of a species. This study has investigated the link between species mean body mass and the height and width of the mandibular corpus in a core sample of 23 species of extant simians. The slopes of the least-squares regressions for the whole sample and for the hominoid subset are similar. However, the intercepts differ so that for a given body mass, a hominoid will generally have a smaller mandible than a generalized simian. The same mandibular measurements were taken on 75 early hominin mandibles assigned to eight species groups. When mandibular corpus height- and width-derived estimates of body mass for the fossil taxa were compared with available postcranial and cranial-derived body mass estimates, the eight early hominin species sort into four groups. The first, which includes A. afarensis and A. africanus, has mandibles which follow a “generalized simian” scaling relationship. The second group, which comprises the two “robust” australopithecine species, P. boisei and P. robustus, has mandibles which scale with body mass as if they are “super-simians,” for they have substantially larger mandibles than a simian with the same body mass. The two “early Homo” species, H. habilis sensu stricto and H. rudolfensis, make up the third group. It has mandibular scaling relationships that are intermediate between that of the comparative simian sample and that of the hominoid subsample. The last of the four groups comprises H. ergaster and H. erectus; their mandibles scale with body mass as if they were hominoids, so that of the four groups they have the smallest mandibles per unit body mass. These results are related to comparable information about relative tooth size. Their relevance for attempts to interpret the dietary adaptations of early hominins are explored. Am J Phys Anthropol 105:523–538, 1998. © 1998 Wiley-Liss, Inc.     

Evolution of photosynthetic reaction centers

The common ancestor of all photosynthetic prokaryotes and organelles contained chlorophyll (Chl) a. All green and purple photosynthetic bacteria descended from a common bacteriochlorophyll (Bchl) a-containing ancestor which diverged from the Chl a line. Separate PS-I and PS-II reaction centers may have evolved before the appearance of Bchl a. When the transition to Bchl a occurred, the resultant organism contained two types of reaction center, “PS-I” and “PS-II.” One line of development eliminated “PS-II” and evolved into the green bacteria. The other line eliminated “PS-I” and became the purple bacteria. In the Chl a-containing organisms the evolution of PS-II continued until oxygen evolution was achieved.     

The systematics of Rigidella (Iridaceae)

Rigidella and the four species contained therein are defined primarily on characters related to, and a direct consequence of, adaptation to hummingbird pollination. The genus is probably derived from either the “multiflora” complex inTigridia subgenusHydrotaenia or is an evolutionary line parallel toTigridia. Illustrations, distribution maps, and a key to the species are included. The rediscovery ofRigidella flammea Lindl. is reported, and a new species,R. inusitata, is described.     

Ultrastructural changes associated with UV irradiation in the "germinal plasm" of Xenopus laevis

To detect structural changes following UV irradiation in the “germinal plasm,” ultrastructure of the “germinal plasm” was studied in normal and UV-irradiated eggs of Xenopus laevis at the following stages: prior to fertilization, early 2-cell, 32-cell, and late blastula. It was revealed that ultrastructural features of the “germinal plasm” were essentially common between Xenopus laevis and Rana pipiens. That is, the “germinal plasm” is composed primarily of a large aggregation of mitochondria and distinctive electron dense bodies (germinal granules). Irregularly shaped cylinderlike granules (giant germinal granules), having the same internal characteristics as the germinal granules, were found in the “germinal plasm” of all eggs examined.Comparison between normal and UV-irradiated eggs has demonstrated that UV irradiation causes swelling and vacuolation of mitochondria and fragmentation of germinal granules. The suggestion is that the integrity of certain UV-sensitive factor(s), which is involved in maintaining normal structure of germinal granules, is indispensable for the determination of the primordial germ cells.     

Nature of the ribosomal RNA transcribed from the X and Y chromosomes of Drosophila melanogaster

In Drosophila melanogaster there is one nucleolar organizer (NO) on each X and Y chromosome. Experiments were carried out to compare the ribosomal RNAs derived from the two nucleolar organizers. ³²PO₄-labelled ribosomal RNA was isolated from two strains of D. melanogaster, one containing only the X chromosome NO, the other containing only the Y chromosome NO. 28 S and 18 S RNA from the two strains were subjected to a variety of “fingerprinting” and sequencing procedures. Fingerprints of 28 S RNA were very different from those of 18 S RNA. Fingerprints of “X” and “Y” 28 S RNA were indistinguishable from each other, as also were fingerprints of “X” and “Y” 18 S RNA. In combined “T₁ plus pancreatic” RNAase fingerprints several distinctive products were characterized and quantitated. Identical products were obtained from X and Y RNA, and the molar yields of the products were indistinguishable. Together these findings imply that the rRNA sequences encoded by the X and Y NOs are closely similar and probably identical to each other.Two further findings were of interest in “T₁ plus pancreatic” RNAase fingerprints: (1) in 28 S (as well as in 18 S) fingerprints several distinctive products were recovered in approximately unimolar yields. This indicates that 28 S RNA does not consist of two identical half molecules, though it does consist of two non-identical half molecules together with a “5.8 S” fragment. (2) Several methylated components in Drosophila rRNA also occur in rRNA from HeLa cells and yeast. This suggests that certain features of rRNA structure involving methylated nucleotides may be highly conserved in eukaryotic evolution.     

Dichilanthe, an unusual Asiatic Rubiaceae with "Lonicera flowers" and "dipterocarp fruits"

Dichilanthe, a disjunctly distributed, arborescent Southeast Asiatic genus (D. zeylanica: Sri Lanka; D. borneensis: West Borneo) with collar-like, persistent stipules, has strongly zygomorphic, ornithophilous flowers which show secondary pollen presentation. The curved corolla is two-lipped. The upper lip consists of 2, and the lower lip of 3 fused corolla lobes. The calyx, too, is zygomorphic. The curved, exserted style ends in a swollen “stylar head' which apically bears two small stigmatic (receptive) areas in a zygomorphic arrangement. The flowers are borne in compact, terminal heads, held together by enlarged stipules of a bract-pair immediately below the inflorescence. The dispersal units (diaspores) mimic dipterocarp fruits. They consist of a persistent, wing-like pair of bracts whose±cuplike stipules enclose the fruits. The diaspores break off at the node immediately below the bract-pair, where there is a distinct abscission zone. Initial on”primary“dispersal by wind may be followed by facultative”secondary“dispersal by floating in water.”Pith tissue“produced by each fruit of the diaspore, and the air spaces contained therein, are likely to be adaptations to floating. This”pith tissue“, a loose, parenchymatic,± irregularly arranged area of the fruit wall which partially disintegrates during fruit maturation, represents a modified portion of the endocarp; the remainder of the endocarp is”normal“sclerenchymatic tissue coating the two locules. The initial stages of this endocarp differentiation are already observable in early developmental stages, i.e., in ovaries of flower buds and open flowers. The bicarpellate ovaries contain a solitary, anatropous pendulous ovule per locule. Viable seeds have large embryos and only c. 5–6 layers of oily endosperm; their exotesta cells have delicate, ring-like thickenings. In developing fruits of individual inflorescences, a high frequency of seed abortion was noted. Not uncommonly, there is only a single viable seed per dispersal unit, i.e., only a solitary seedling emerging from a diaspore. Germination of the seeds is cryptocotylar. The pollen of D. zeylanica is suboblate and 5- or 6-colpate (with the colpi being rather short); the exine is finely reticulate. In spite of several of its character states being unusual and aberrant, the tribal position of Dichilanthe in the Guettardeae is not questioned, although it is concluded that the genus occupies a rather isolated position in the tribe.     

Role of genes O and P in the replication of bacteriophage lambda DNA.

DNA replication in coliphage λ occurs in two stages. The first round of replication generates mainly circular progeny DNA by a double-branched θ-type replicative form (Ogawa et al., 1968; Schnös &; Inman, 1970). In the late stage of λ DNA replication, however, σ-type rolling-circle replicative form DNA molecules, which produce multigenomic linear concatemers, are primarily found (Takahashi, 1974).At both early and later times, a temperature shift of λ Ots or Pts infected cells from 32 °C (permissive) to 43 °C (non-permissive temperature) caused a rapid reduction of the rate of radioactive precursor incorporation into λ DNA, showing that the gene O and P products are essential for the continuation of λ DNA synthesis. Observations on the molecular fine structure of the replicating fork after a temperature shift revealed characteristic long “single-strand connections” and single-strand “whiskers” at the branch point. These observations suggest that λ gene O and P products are directly involved in the propagation of daughter strands.     

Morphology of the mouthparts of the spittlebug Philagra albinotata Uhler (Hemiptera: Cercopoidea: Aphrophoridae)

Mouthparts associated with feeding behavior and feeding habits are important sensory and feeding structures in insects. To obtain a better understanding of feeding in Cercopoidea, the morphology of mouthparts of the spittlebug, Philagra albinotata Uhler was examined using scanning electron microscopy. The mouthparts of P. albinotata are of the typical piercing–sucking type found in Hemiptera, comprising a cone-shaped labrum, a tube-like, three-segmented labium with a deep groove on the anterior side, and a stylet fascicle consisting of two mandibular and two maxillary stylets. The mandibles consist of a dorsal smooth region and a ventral serrate region near the apical half of the external convex region, and bear five nodules or teeth on the dorsal external convex region on the distal extremity; these are regarded as unique features that distinguish spittlebugs from other groups of Hemiptera. The externally smooth maxillary stylets, interlocked to form a larger food canal and a smaller salivary canal, are asymmetrical only in the internal position of longitudinal carinae and grooves. One dendritic canal is found in each maxilla and one in each mandible. Two types of sensilla trichodea, three types of sensilla basiconica and groups of multi-peg structures occur in different locations on the labium, specifically the labial tip with two lateral lobes divided into anterior sensory fields with ten small peg sensilla arranged in a 5 + 4 + 1 pattern and one big peg sensillum, and posterior sensory fields with four sensilla trichodea. Compared with those of previously studied Auchenorrhyncha, the mouthparts of P. albinotata may be distinguished by the shape of the mandibles, the multi-peg structures and a tooth between the salivary canal and the food canal on the extreme end of the stylets. The mouthpart morphology is illustrated using scanning electron micrographs, and the taxonomic and putative functional significance of the different structures is briefly discussed.     

Middle Givetian echinoderms from the Schlade Valley (Rhenish Massif,Germany): habitats,taxonomy and ecostratigraphy

Crinoids and ophiocistioids from classical fossil localities of the National Geosite “Schlade Valley”, NE of Bergisch Gladbach (Germany) are reported for the first time. The fossils were derived from the reefal Büchel Formation (lowermost Middle Givetian, Middle Devonian) at the northern flank of the Bergisch Gladbach-Paffrath Syncline (eastern Rhenish Massif). From the abandoned quarry “Im Grubenfeld”, skeletal elements of holothuroids, ophiocistioids and crinoids are documented from a bituminous marly shale horizon in the middle Büchel Formation. The finely bedded shales suffocated an already stressed, muddy “reefal” fauna, which followed on top of a massive Actinostroma stromatoporoid biostrome. The shales characterise an apparently regionally occurring event, herein denominated as “Schlade Event”. It is considered to represent the climax of the transgressive Lower pumilio Event. The autochthonous and vagile epibenthic echinoderm fauna on top of the “Schlade Event Layer” is low diverse. It is regarded, herein, as post disaster fauna, recolonising the dysaerobic softground/soupground together with the well-adapted trilobite Goldius. The cupressocrinitids Halocrinites and Procupressocrinus were recognised from a younger stratum of the upper Büchel Formation within the abandoned “Zimmermann Quarry” near-by. The crinoids settled in high-energy environments of a reef flat in association with characteristic brachiopods (Uncites, Stringocephalus) and bivalves (Eomegalodon) and were swept by storms into reef flat pools. In those exceptional fossil lagerstätten, which are marl-filled obrution deposits, they were parautochthonously preserved together with an autochthonous fauna composed mostly of gastropods and extremely rare allochthonous biota from the open marine realm. Published biozonations of the Büchel Formation, especially on ammonoids, are evaluated, partly corrected and supplemented by ecostratigraphic associations of rugose corals and crinoids. Schlade Event below and Taghanic Event above are major factors controlling biozonation. Taxonomic notes concern revision of the holothuroids from the Schlade Valley and discussion of taxonomic attribution of ophiocistoids and crinoids. All species formerly included in “Abbreviatocrinites” are transferred to genus Halocrinites, which has priority.     

Salivary glands in Cicadidae (Hemiptera: Cicadoidea): comparative morphology, ultrastructure, and their phylogenetic significance

The present investigation provides information on gross morphology and ultrastructure of salivary glands of species in Cicadidae in detail. The structure of the salivary glands of 11 representative species from 10 genera belonging to three subfamilies of Cicadidae was studied using light microscopy and transmission electron microscopy. In the examined species, the salivary glands are paired structures, and each of which is comprised of a principal gland (pg) and an accessory gland (ag). The pg is divided into anterior and posterior lobes, and both of which consist of numerous long digitate lobules. The lobules at the base of the long digitate lobules of posterior lobe are greatly short; here, we named as “short lobules.” All the lobules vary in size, disposition, length, and shape. The anterior lobe and posterior lobes are connected by an anterior–posterior duct (apd). Two efferent salivary ducts (esd), derived from corresponding posterior lobes, fuse to form a short common duct which enters into the saliva syringe. The ag is composed of a greatly tortuous and folded accessory salivary tube, a gular gland (gg) constituting of several acini, and an accessory salivary duct (asd). The asd joins the esd at the place where the latter emergences. Constituents and arrangement of the salivary glands, the number and shape of the long digitate lobules in the anterior and posterior lobes, and the visibility of the apd were promising characters for the taxonomic and phylogenetic analysis of Cicadoidea. The variations of secretory granules in size, shape, and electron density in lobule cells of pg of Platypleura kaempferi probably indicating different materials are synthesized. The absence of the infoldings of basal plasma membrane in the basal area of the cells and the presence of electron-lucent vesicles in the cytoplasm of the gg cells of P. kaempferi might suggest that the secretions of gg are more watery.     

Systematic implications of the peroxidase isoenzymes in the Xanthium strumarium complexes

Starch-slab gel electrophoresis showed two patterns of peroxidase isoenzymes in the polymorphic taxon. Xanthium strumarium L. The “strumarium” morphological complex (X. strumarium, in the sense of Millspaugh and Sherff), the putative indigenous plants of the Old World, contained a different pattern from that shown by putative introductions from the New World. Experimental F₁ hybrids between “strumarium” and other complexes, “italicum-pennsylvanicum”, “chinense”, “oviforme” and “cavanillesii”, had the peroxidase pattern of the American plants. These peroxidase isoenzyme patterns were not influenced by the environmental growing conditions, but, along with partial genetic incompatibility, support the taxonomic separation of X. strumarium from other taxa of section Euxanthium.     

Studies of the metathorax of the trout-stream beetle,Amphizoa lecontei Matthews (Coleoptera : Amphizoidae): Contribution towards clarification of the systematic position of Amphizoidae

Skeleton and musculature of the metathorax and the abdominal nerve cord of Amphizoa lecontei (Coleoptera : Amphizoidae) Matthews were examined and compared to those of other members of Adephaga (Coleoptera). The following characters may be important for phylogenetic analysis. The narrow prescutal area and moderately developed mesophragma with distinctly separated median phragmal lobes in Amphizoa is considered as plesiomorphic, whereas the median phragmal lobes lying closely together or fused is a possible synapomorphy of Hygrobiidae and Dytiscidae. The short 1st axillary sclerite of Amphizoa may be an autapomorphy of the group. The weakly arched notum and the poorly developed metaphragma arc obviously the result of tendency towards flightlessness. The anepisternum meets the middle coxal cavity. The prosternal process does not reach the meta “sternum” (“sternum” = preepisternum + basisternum presternum + spinasternum 2). The specialized pro-meso-meta “sternal” articulation in Hygrobia and Dytiscidae is considered a synapomorphy of both groups. The amphizoid metafurca is distinctly reduced in size. Pouch-like anterolateral excavations are considered plesiomorphic. Strong dorsolateral and weak ventrolateral projections of the metafurca may be a synapomorphy of Hygrobiidae and Dytiscidae. The hind legs of Amphizoa are not adapted for swimming, except for very sparse fringes of thin setae. Swimming hind legs are considered as a synapomorphy of Hygrobiidae and Dytiscidae. The main flight muscles were degenerated in all specimens of Amphizoa examined. Absence of muscle (M) 65 may be autapomorphic for Amphizoidae. Presence of M 72 is a symplesiomorphy of Amphizoidae and Dytiscidae. M 81 and M 83 arc absent. The strong M 82 is considered as plesiomorphic. The moderate size of M 85 is connected with the lack of swimming ability. The elongate abdominal nerve cord in Amphizoa points towards a sistergroup relationship between Hygrobiidae and Dytiscidae in both of which the abdominal nerve cord shows a high degree of fusion.The phylogenetic propositions of Baehr (1979), and Kavanaugh (1986), are not consistent with the interpretation provided herein, whereas the conclusions of Burmeister (1976), Ruhnau (1986) and Beutel (1986) seem to correlate well. Therefore, it is suggested that the Amphizoidae are the sistergroup of Hygrobiidae + Dytiscidae.