Karyological knowledge of the Italian vascular flora as inferred by the analysis of “Chrobase.it”

Abstract

Chromosome number knowledge of the Italian vascular flora is stored in the online database Chrobase.it, which includes 6723 records, referable to 3428 taxa, 2799 accepted species and subspecies (about 35% of the national flora), and 3410 different chromosome countings (cytotypes). Appropriate queries to Chrobase.it allowed us to calculate mean, modal and median chromosome numbers for the Italian vascular flora, for geographical subgroups (islands, south, centre, north) and for selected orders, families and genera. Chromosome number data were available for 41 out of 55 orders (74%) and 107 out of 428 families (67%), represented by 664 out of 1297 genera (51%). The most studied administrative regions are Sicily (844 taxa), Tuscany (592 taxa), and Sardinia (390 taxa), while the most studied families are Asteraceae (465 taxa), Fabaceae (266 taxa), Brassicaceae (158 taxa), and Poaceae (144 taxa). Chromosome numbers range from 2n = 6, occurring in several species of Hypochaeris (Asteraceae), to 2n = 240, occurring in Ophioglossum (Ophioglossaceae), Dryopteris (Dryopteridaceae) and Arenaria (Caryophyllaceae) (mode is 2n = 18, and median is 2n = 24). Chromosome number variability was analyzed by frequencies (linear plots) and ANOVA, resulting in significant differences among geographical groups (mean chromosome number increasing from islands-south to centre-north) and selected taxa. B-chromosomes occur in 5.3% of data (148 taxa) and their number is not significantly different among geographical areas, while they occur only in 14 orders, 17 families, and 56 genera. The number of B-chromosomes ranges from 1 to 13 (mode = 1, median = 2).     

The biology and ecology of lotic microcrustaceans

• 1 Copepoda, Ostracoda and ‘Cladocera’ are important meiobenthic Crustacea which can be both numerically abundant and species rich in running waters. Harpacticoids and ostracods are well adapted to benthic life because they are typical crawlers, walkers, and burrowers. Many cladocerans are substratum dwellers, but most benthic species among these can also swim. Cyclopoids which are generally good swimmers are nevertheless often bottom frequenters and actively colonise sediment interstices (the hyporheic zone).
  • 2 The subclass Copepoda includes 10 orders. With 53 families, the order Harpacticoida dominates the benthos. Only five of these families are represented in fresh waters (ca. 1 000 species and subspecies). The order Cyclopoida includes 12 families of which the Cyclopidae is well represented in freshwater habitats with 900 species and subspecies. Freshwater Ostracods belong to the order Podocopida (5 000 species) with three superfamilies occurring in running fresh waters. The group ‘Cladocera’ contains four orders, 12 families, more than 80 genera, and 450–600 freshwater species. Most of the benthic species are found in the families Chydoridae (39 genera), Macrothricidae, Ilyocryptidae and Sididae.
• 3 For each of the three major taxa, morphological characteristics are presented, specimen collection and preparation are described and references to available taxonomical keys are provided.
• 4 Biological characteristics are extremely diverse among and within the three taxa, resulting in a great variety of strategies in meiobenthic crustaceans. Characteristics of reproduction, sexual dimorphism, cyclomorphosis and population parameters (i.e. clutch size, lifespan, growth, moulting) are provided for some of the most common species.
• 5 Important differences between the three main taxa were found at the species level. Ecological requirements such as hydraulic microhabitats and geomorphologic features of the streambed are the major determinants of species diversity and abundance for benthic microcrustacea of lotic habitats. Many studies on the ecology of these communities are limited by a lack of knowledge of the life history characterisitics of lotic (especially interstitial) crustacean populations.

     

Embriologia Della “Periploca Graeca“ L

Abstract

This article presents results of a field survey of pollinators of two Apocynaceae, Periploca laevigata subsp. angustifolia (Labill.) Markgraf (Periplocoideae) and Caralluma europaea (Guss.) N.E.Br. (Asclepiadoideae) co-occurring on Lampedusa Island, Mediterranean sea. Fifteen species within nine families of Diptera have been identified as pollinators of the two plants. The families involved are Tephritidae, Milichiidae, Trixoscelididae, Scathophagidae, Anthomyiidae, Muscidae, Calliphoridae, Sarcophagidae, Rhinophoridae. Families of Muscidae and Sarcophagidae are the more represented, respectively with four and three species. P. laevigata subsp. angustifolia seems to have a broader spectrum of pollinators, with 12 species of Diptera involved, while C. europaea has 8 species of Diptera as pollinators. Five species of Diptera are shared between the two plant species. The presented data are the first records of pollinators for P. laevigata subsp. angustifolia and C. europaea and confirm that both taxa are fly pollinated, though they do not conform exactly to the sapromyiophilous syndrome. The number of pollinators identified indicated that the morphological and functional floral specialization of the two taxa cover a wide number of pollinators with a similar biology.     

The promotive effect of smoke derived from burnt native vegetation on seed germination of Western Australian plants

Exposure of dormant seed to cold smoke derived from burnt native vegetation had a positive influence on germination in one or more seed provenances in 45 out of 94 species of native Western Australian plants that are normally hard to germinate. When tested under controlled conditions some species showed earlier germination in smoke treatments than controls; in others smoke-treated seeds continued to germinate for several weeks after controls had achieved full germination. In the remainder, treated and control seeds germinated to similar time schedules. A group of 23 species which responded positively had previously been recorded as extremely difficult or impossible to germinate using conventional techniques. These included members of the genera Geleznowia (Rutaceae), Hibbertia (Dilleniaceae), Stirlingia (Proteaceae), Verticordia (Myrtaceae), Actinostrobus (Cupressaceae) and Pimelea (Thymelaeaceae). Both large- and small-seeded species were encountered amongst the positively responding taxa, which encompassed representatives of 15 families and 26 genera of dicotyledons, 5 families and 8 genera of monocotyledons and the gymnosperm Actinostrobus acuminatus. Sowing seeds on smoke-fumigated filter papers or watering with aqueous eluates of smoke elicited similar degrees of stimulation of germination, as did exposure to gaseous smoke in a readily germinating species Anigozanthos manglesii (Haemodoraceae) and the normally intractable species Lysinema ciliatum (Epacridaceae). Exposing recently burnt and unburnt natural bushland sites to smoke, smoked water or smoked dry sand elicited a significant germination response in 15 species. Over one third of the species sampled in the burnt site exhibited germination additional to that caused by the fire. Data are discussed in relation to previous germination studies on Australian and other taxa.     

COLEOFASCICULUS GEN. NOV. (CYANOBACTERIA): MORPHOLOGICAL AND MOLECULAR CRITERIA FOR REVISION OF THE GENUS MICROCOLEUS GOMONT1

Species currently classified within the cyanobacterial genus Microcoleus were determined to fall into two distinct clades in a 16S rDNA phylogeny, one containing taxa within the Oscillatoriaceae, the other containing taxa within the Phormidiaceae. The two lineages were confirmed in an analysis of the 16S–23S internal transcribed spacer (ITS) region sequences and secondary structures. The type species for Microcoleus is M. vaginatus Gomont, and this taxon belongs in the Oscillatoriaceae. Consequently, Microcoleus taxa in the Phormidiaceae must be placed in separate genera, and we propose the new genus Coleofasciculus to contain marine taxa currently placed in Microcoleus. The type species for Coleofasciculus is the well‐studied and widespread marine mat‐forming species Microcoleus chthonoplastes (Mert.) Zanardini ex Gomont. Other characters separating the two families include type of cell division and thylakoid structure.     

Form-Pfs Plastids,Stem Anatomy and Systematic Affinities of Stylobasium Desf. (Stylobasiaceae)

The vascular system of the stem of Stylobasium was investigated during its primary and secondary phases with both light and electron microscopic methods. It contains collateral bundles arranged in a ring, separated by rays which undergo regular cambial growth. The phloem consists of short sieve elements connected to sieve tubes by simple sieve plates, companion cells of the same length, and phloem parenchyma cells. During their autophagy-like differentiation and maturation, typical of all angiosperms, the sieve elements of Stylobasium have a peculiar feature, whereby they develop and retain form-Pfs plastids (containing protein filaments and starch). The sieve-element plastids of the two Stylobasium species, and of some 100 species belonging to taxa of which Stylobasium had been considered to be a possible member, have been studied by transmission electron microscopy. With the exception of a few species with form-Pcs plastids (containing a single small protein crystal in addition to starch), the great majority of taxa studied are characterized by S-type sieve-element plastids (containing starch only). The presence of form-Pfs plastids in Stylobasium supports its separation into the unigeneric Stylobasiaceae and the placement of this family close to other form-Pfs or form-Pcfs-containing taxa. While other characters would exclude an affiliation to the Magnolianae (form-Pfs plastids in Canella) or Caryophyllales (form-Pfs plastids in Microtea), an association with the form-Pcfs families Connaraceae and Mimosaceae is positively considered and corresponds to their frequent allocation close to the Rutales and Sapindales. Within the Rutales/Sapindales the sizes of sieve-element plastids (average diameter) range from very large (e.g. in the Julianaceae) to comparatively small (e.g. in Aceraceae) and are used to group the families. The sieve element characters of the Coriariaceae (tiny plastids with almost no starch, wide sieve plate pores, copious P-protein) suggest their removal from Rutales/Sapindales into the neighbourhood of the Cucurbitaceae.     

Diversity, Distribution, and Ancient Taxonomic Relationships Within the TIR and Non-TIR NBS-LRR Resistance Gene Subfamilies

Phylogenetic relationships among the NBS-LRR (nucleotide binding site–leucine-rich repeat) resistance gene homologues (RGHs) from 30 genera and nine families were evaluated relative to phylogenies for these taxa. More than 800 NBS-LRR RGHs were analyzed, primarily from Fabaceae, Brassicaceae, Poaceae, and Solanaceae species, but also from representatives of other angiosperm and gymnosperm families. Parsimony, maximum likelihood, and distance methods were used to classify these RGHs relative to previously observed gene subfamilies as well as within more closely related sequence clades. Grouping sequences using a distance cutoff of 250 PAM units (point accepted mutations per 100 residues) identified at least five ancient sequence clades with representatives from several plant families: the previously observed TIR gene subfamily and a minimum of four deep splits within the non-TIR gene subfamily. The deep splits in the non-TIR subfamily are also reflected in comparisons of amino acid substitution rates in various species and in ratios of nonsynonymous-to-synonymous nucleotide substitution rates (K _A/K _S values) in Arabidopsis thaliana. Lower K _A/K _S values in the TIR than the non-TIR sequences suggest greater functional constraints in the TIR subfamily. At least three of the five identified ancient clades appear to predate the angiosperm–gymnosperm radiation. Monocot sequences are absent from the TIR subfamily, as observed in previous studies. In both subfamilies, clades with sequences separated by approximately 150 PAM units are family but not genus specific, providing a rough measure of minimum dates for the first diversification event within these clades. Within any one clade, particular taxa may be dramatically over- or underrepresented, suggesting preferential expansions or losses of certain RGH types within particular taxa and suggesting that no one species will provide models for all major sequence types in other taxa. Received: 13 June 2001 / Accepted: 22 October 2001     

PHYLOGENETIC ANALYSES OF THE RED ALGAL ORDER RHODYMENIALES SUPPORTS RECOGNITION OF THE HYMENOCLADIACEAE FAM. NOV., FRYEELLACEAE FAM. NOV., AND NEOGASTROCLONIUM GEN. NOV.1

Systematics of the red algal order Rhodymeniales was investigated using combined large‐subunit nuclear ribosomal DNA (LSU) and elongation factor 2 (EF2) analyses. These data were subjected to distance, parsimony, and Bayesian analyses, and the resulting phylogenies were largely congruent with previously published SSU results in that the four currently recognized rhodymenialean families (Champiaceae, Faucheaceae, Lomentariaceae, and Rhodymeniaceae) were resolved as monophyletic lineages (with the exception of Coelothrix, which is here transferred to the Champiaceae from the Rhodymeniaceae). In addition, taxa presently considered as incertae sedis consisted of two lineages (Fryeella lineage and Hymenocladia lineage). Based on these results, two new families are proposed: (i) the Fryeellaceae fam. nov. to accommodate the genera Fryeella, Hymenocladiopsis, and a new taxon from Tasmania, Australia; and (ii) the Hymenocladiaceae fam. nov., to accommodate Asteromenia, Hymenocladia, and Erythrymenia. In addition to resolving familial relationships, these analyses resolved some novel interspecific affinities, and we propose a new genus, Neogastroclonium gen. nov., for Gastroclonium subarticulatum, a species that differs significantly in both morphology and molecular data from genuine species of Gastroclonium. Relationships among additional faucheacean and lomentariacean taxa were investigated using LSU data only, and these results are discussed. The familial classification of the Rhodymeniales proposed herein is discussed in light of vegetative and reproductive anatomy, most notably the ontogeny of the tetrasporangia.     

Mammalian Diet and Broad Hunting Strategy of the Dingo (Canis familiaris dingo) in the Wet Tropical Rain Forests of Northeastern Australia1

The diet of dingoes (Canis familiaris dingo) in the Australian Wet Tropics was examined by analyzing 383 dingo scats collected throughout the region for the presence of mammal prey remains. The scats yielded 29 native and 4 introduced mammal prey species from 14 families. The most important species in terms of percentage occurrence in the scats were Melomys cervinipes (22.2%), hoodon macrourus (17.0%), Perameles nasuta (12.5%), and Thylogale stigmatica (12.5%). The most important families were Muridae (37.1%), Peramelidae (29.5%), and Macropodidae (25.8%). Examination of small‐scale habitat preferences revealed species that preferentially use the forest edge ranked significantly higher in the diet than those that do not, and species that are terrestrial ranked higher in the diet than those that are arboreal. Relative abundance was also a significant factor in the ranked dietary occurrence of each species, with abundant species ranked significantly higher than those that are less abundant. These results suggest that dingoes in the Australian Wet Tropics are opportunistic predators of a wide variety of mammal species, with abundant terrestrial and forest edge‐dwelling taxa the most susceptible to predation.     

The impacts of rats on the endangered native flora of French Polynesia (Pacific Islands): drivers of plant extinction or coup de grâce species?

Although rats have clearly contributed to bird extinctions on islands, their role in plant extinctions is not as clear. Paleoenvironmental studies suggest rats were responsible for the demise of several island palm species. French Polynesia’s islands provide an opportunity to evaluate “modern” impacts of rats on native flora. Our study shows that 15 threatened taxa (nine families) are damaged by rats. All 12 subjected to seed predation are woody plants with large-seeded drupes. Three experience severe predation and recruitment depression (Santalum insulare, Ochrosia tahitensis, Nesoluma nadeaudii). Three-year monitoring of Polynesian sandalwood (Santalum insulare) populations in Tahiti during rat control suggested that over 99% of fruits were eaten before ripening. Seed predation on sandalwood appeared to be lower on islands without black rats Rattus rattus. Studies from Indo-Pacific islands document rat impact on at least 56 taxa (28 families). Certain families (Arecaceae, Elaeocarpaceae, Rubiaceae, Santalaceae, and Sapotaceae) are particularly vulnerable to seed predation. Other soft-barked trees (Araliaceae, Euphorbiaceae, and Malvaceae) suffer from stem or bark damages, especially during dry seasons. Although rats depress seedling recruitment and alter vegetation dynamics, no evidence demonstrates that they are solely responsible for current plant extinctions. Most of French Polynesia’s endangered species impacted by rats occur in severely degraded habitats. We therefore suggest that rats can be viewed more as coup de grace species (i.e., that give the final stroke of death), rather than as main drivers of plant extinctions. More research is needed to clarify the impacts of rat species and their importance in plant population decline or demise.     

Synopsis of a new collection of sea spiders (Arthropoda: Pycnogonida) from the Ross Sea,Antarctica

The biodiversity research expedition TAN0204 with RS Tangaroa to the Ross Sea in 2004 yielded a new collection of 2,687 specimens of pycnogonids. As much as 25 different species encompassing 14 genera and eight families were identified and their records are discussed herein. The collection is archived in the Marine Invertebrate Collection of the New Zealand National Institute of Water and Atmospheric Research (NIWA). The majority (69%) of specimens are from the Nymphon australe group (Nymphonidae), although species richness and abundance varied among the stations sampled. The collection includes several specimens from polymerous taxa; Pentanymphon antarcticum (Nymphonidae), Decolopoda australis (Colossendeidae) and Pentapycnon bouvieri (Pycnogonidae). All species were classified based on morphological characters, and DNA sequences (from the 18S, 12S, 16S and COI regions) for 21 of the representative morphotypes are given. The DNA sequences confirmed the species-level distinctiveness of these morphotypes. No species new to science were identified, although further detailed morphometric and/or molecular analyses may reveal cryptic or sibling species, especially in species such as the highly abundant Nymphon australe group. An erratum to this article can be found at     

Comparative analysis of genome composition in Triticeae reveals strong variation in transposable element dynamics and nucleotide diversity

A 454 sequencing snapshot was utilised to investigate the genome composition and nucleotide diversity of transposable elements (TEs) for several Triticeae taxa, including Triticum aestivum, Hordeum vulgare, Hordeum spontaneum and Secale cereale together with relatives of the A, B and D genome donors of wheat, Triticum urartu (A), Aegilops speltoides (S) and Aegilops tauschii (D). Additional taxa containing the A genome, Triticum monococcum and its wild relative Triticum boeoticum, were also included. The main focus of the analysis was on the genomic composition of TEs as these make up at least 80% of the overall genome content. Although more than 200 TE families were identified in each species, approximately 50% of the overall genome comprised 12–15 TE families. The BARE1 element was the largest contributor to all genomes, contributing more than 10% to the overall genome. We also found that several TE families differ strongly in their abundance between species, indicating that TE families can thrive extremely successfully in one species while going virtually extinct in another. Additionally, the nucleotide diversity of BARE1 populations within individual genomes was measured. Interestingly, the nucleotide diversity in the domesticated barley H. vulgare cv. Barke was found to be twice as high as in its wild progenitor H. spontaneum, suggesting that the domesticated barley gained nucleotide diversity from the addition of different genotypes during the domestication and breeding process. In the rye/wheat lineage, sequence diversity of BARE1 elements was generally higher, suggesting that factors such as geographical distribution and mating systems might play a role in intragenomic TE diversity.     

Colonization of the deep sea by fishes

Analysis of maximum depth of occurrence of 11 952 marine fish species shows a global decrease in species number (N) with depth (x; m): log₁₀N = ?0·000422x + 3·610000 (r² = 0·948). The rate of decrease is close to global estimates for change in pelagic and benthic biomass with depth (?0·000430), indicating that species richness of fishes may be limited by food energy availability in the deep sea. The slopes for the Classes Myxini (?0·000488) and Actinopterygii (?0·000413) follow this trend but Chondrichthyes decrease more rapidly (?0·000731) implying deficiency in ability to colonize the deep sea. Maximum depths attained are 2743, 4156 and 8370 m for Myxini, Chondrichthyes and Actinopterygii, respectively. Endemic species occur in abundance at 7–7800 m depth in hadal trenches but appear to be absent from the deepest parts of the oceans, >9000 m deep. There have been six global oceanic anoxic events (OAE) since the origin of the major fish taxa in the Devonian c. 400 million years ago (mya ). Colonization of the deep sea has taken place largely since the most recent OAE in the Cretaceous 94 mya when the Atlantic Ocean opened up. Patterns of global oceanic circulation oxygenating the deep ocean basins became established coinciding with a period of teleost diversification and appearance of the Acanthopterygii. Within the Actinopterygii, there is a trend for greater invasion of the deep sea by the lower taxa in accordance with the Andriashev paradigm. Here, 31 deep‐sea families of Actinopterygii were identified with mean maximum depth >1000 m and with >10 species. Those with most of their constituent species living shallower than 1000 m are proposed as invasive, with extinctions in the deep being continuously balanced by export of species from shallow seas. Specialized families with most species deeper than 1000 m are termed deep‐sea endemics in this study; these appear to persist in the deep by virtue of global distribution enabling recovery from regional extinctions. Deep‐sea invasive families such as Ophidiidae and Liparidae make the greatest contribution to fish fauna at depths >6000 m.     

An integrative approach to characterize Malagasy bats of the subfamily Vespertilioninae Gray, 1821, with the description of a new species of Hypsugo

Although important advances have been made in recent years in the taxonomy of different families and subfamilies of Malagasy bats, those belonging to the Vespertilioninae remain partially unresolved. Herein using a mitochondrial marker (cytochrome b) as the point of departure for 76 specimens of Malagasy vespers and appropriate African taxa, we diagnose the six taxa of this subfamily on the island by overlaying different morphological and bioacoustic characters on the clade structure of sequenced animals. The species include: endemic Neoromicia matroka, which is sister to African N. capensis; endemics N. malagasyensis and N. robertsi, which form sister species; a member of the genus Hypsugo, which is sister to African H. anchietae and described herein as new to science; Pipistrellus hesperidus for which Madagascar animals are genetically close but distinct from African populations of the same species; and endemic P. raceyi, which shows segregation of eastern (mesic) and western (dry) populations and its sister species relationships are unresolved. While the external and craniodental measurements, as well as bioacoustic variables, allow only partial differentiation of these six species of Vespertilioninae, molecular characters provide definitive separation of the taxa, as do male bacular morphology. © 2015 The Linnean Society of London     

Radiolarian taxa from Southern Ocean sediment traps (Atlantic sector)

Summary This study gives a first inventory of radiolarian taxa collected with sediment traps in different areas of the Southern Ocean (Drake Passage, Powell Basin and Bransfield Strait). It includes 66 taxa or taxa groups of which 46 were already described. Two previously described species groups and 20, yet undescribed, taxa are documented. The name Protocystis bicornis (Haecker) is replaced by P. spinosus as it is a later homonym of P. bicornis (Borgert). The occurrence pattern of the radiolarian taxa indicates distinct differences in the species composition between neritic environments (Bransfield Strait and Powell Basin) and pelagic, open ocean conditions (Drake Passage).     

Beyond Masses and Blooms: The Indicative Value of Oligochaetes

The European Water Framework Directive (WFD) defines a framework for assessing water bodies in Europe in the future. The conditions in the Directive impose a strong demand for “new” assessment systems. The AQEM project developed an assessment system for European streams using macroinvertebrates. Almost 900 samples were taken in about 400 streams covering 29 stream types distributed over eight countries. The role of the Oligochaeta within this European database was analysed. Almost half a million specimens of oligochaetes were collected in 772 samples. Eight families, 41 genera and 69 species were recorded, although identification emphasised the families Tubificidae and Naididae. Three countries identified oligochaetes to species level, most others restricted their identifications to easy identifiable taxa. Numbers of specimens, species, genera and families differed strongly between the countries due to method, although standardised, and taxonomic knowledge. About 50% of all collected oligochaete taxa had assigned biological and ecological indicator values for metric calculation in the AQEM assessment system. A further refinement of this indication list as well as increased coverage of oligochaete taxa was advised. Weighted averaging was used to evaluate the relation between oligochaete distribution and ecological quality class. It was concluded that when higher taxonomic levels are used in assessment, the quality evaluation results become biased. Furthermore, oligochaetes can tell us much more about the ecological status of streams than is commonly assumed. Differences in ecological optima among Limnodrilus udekemianus, Ilyodrilus templetoni, Aulodrilus pluriseta, Nais communis, and Spirosperma ferox are shown.     

Repeated convergent evolution of parthenogenesis in Acariformes (Acari)

The existence of old species‐rich parthenogenetic taxa is a conundrum in evolutionary biology. Such taxa point to ancient parthenogenetic radiations resulting in morphologically distinct species. Ancient parthenogenetic taxa have been proposed to exist in bdelloid rotifers, darwinulid ostracods, and in several taxa of acariform mites (Acariformes, Acari), especially in oribatid mites (Oribatida, Acari). Here, we investigate the diversification of Acariformes and their ancestral mode of reproduction using 18S rRNA. Because parthenogenetic taxa tend to be more frequent in phylogenetically old taxa of Acariformes, we sequenced a wide range of members of this taxon, including early‐derivative taxa of Prostigmata, Astigmata, Endeostigmata, and Oribatida. Ancestral character state reconstruction indicated that (a) Acariformes as well as Oribatida evolved from a sexual ancestor, (b) the primary mode of reproduction during evolution of Acariformes was sexual; however, species‐rich parthenogenetic taxa radiated independently at least four times (in Brachychthonioidea (Oribatida), Enarthronota (Oribatida), and twice in Nothrina (Oribatida), (c) parthenogenesis additionally evolved frequently in species‐poor taxa, for example, Tectocepheus, Oppiella, Rostrozetes, Limnozetes, and Atropacarus, and (d) sexual reproduction likely re‐evolved at least three times from species‐rich parthenogenetic clusters, in Crotonia (Nothrina), in Mesoplophora/Apoplophora (Mesoplophoridae, Enarthronota), and in Sphaerochthonius/Prototritia (Protoplophoridae, Enarthronota). We discuss possible reasons that favored the frequent diversification of parthenogenetic taxa including the continuous long‐term availability of dead organic matter resources as well as generalist feeding of species as indicated by natural variations in stable isotope ratios.     

Sieve-Element Plastids,Nuclear Crystals and Phloem Proteins in the Zingiberales

The sieve-element characters of 40 species from all families making up the monocotyledon order Zingiberales have been studied by transmission electron microscopy. While phloem-proteins are a typical component of all eight families, the Zingiberaceae are characterized by nondispersive protein bodies derived from nuclear crystals. The sieve-element plastids are of the form-P2cs, i.e. contain cuneate protein crystals (as typical of all monocotyledons) and starch grains, those of the family Musaceae have protein filaments in addition (form-P2cfs). The exclusiveness of the form-P2c(f)s plastids contributed to the homogeneity of the order and its distinctness among other monocotyledon taxa. When diameters of the sieve-element plastids from leaf phloem are compared, in the “banana group” the family averages of the Strelitziaceae and the Lowiaceae have, respectively, maximum and minimum values and are clearly different from those in the Musaceae, the family in which they have been included previously. In the “ginger group”, the family averages of the Zingiberaceae, Costaceae, and Marantaceae are close to the order average, with only Cannaceae having minimum values. A comparison of species averages, however, reduces the size differences between families: the value for Ravenala (Strelitziaceae) is close to those of the five Musaceae tested, and that of Globba (Zingiberaceae) even slightly lower than the species average of Canna.     

How many species of Cladocera are there?

An estimation of the number of taxa within families, genera and local faunas of Cladocera reveals that only c. 129 species (17% of all known species) may be considered as sufficiently well described (valid species), and c. 146 as rather well described (fair species) but needing further study using modern methods of investigation. The status of all other species is vague. The families Chydoridae, Daphniidae and Sididae and genera Diaphanosoma, Daphnia, (including Daphniopsis), Megafenestra, Scapholeberis, Eurycercus, Chydorus, Ephemeroporus and Pleuroxus have been comparatively studied best. The largest number of valid species is known from Europe, North America, Australia and South America, and the smallest number from Africa. Presence of large number of vague species of Cladocera negatively affects faunistic, zoogeographic, and ecological studies of continental waters.Dedicated to the memory of Professor D. J. Frey