Behaviour and dispersal in adult Taeniopteryx nebulosa (Linnaeus, 1758) and Perlodes microcephalus (Pictet, 1833) (Plecoptera) in Denmark

Adult Taeniopteryx nebulosa (Linnaeus, 1758 Linnaeus, C. (1758), Systema Naturae (10th ed.), Tom 1, Holmiae. [Google Scholar]) and Perlodes microcephalus (Pictet, 1833 Pictet, J., (1833), ‘Memoire sur la Metamorphoses des Perles’, Annales des Sciences Naturelles, XXVII, 44–55. [Google Scholar]) emerge late winter to early spring in Danish streams. Based on 13 years of study, we have provided new data and discussed little-known aspects of biology of these two species. Taeniopteryx nebulosa male deposits a spermatophore on the female gonopore. Both species are poor fliers and seek high posts for take-off, where they thermoregulate by basking in a pre-flight sun posture for heating flight muscles. Oviposition flight is erratic and short. The females skim back to land. Taeniopteryx nebulosa eggs drift a long distance as single eggs before adhering to vegetation. Perlodes microcephalus eggs drift a short distance as intact eggpackets before they fasten and disintegrate on the bottom. Perlodes microcephalus females select oviposition sites on or close to upstream a riffle. This is critical in ensuring that eggs fasten on stable gravel and stone bottoms. The fast recolonisation of P. microcephalus in Danish streams following restoration measures indicates efficient dispersal ability despite poor flight performance. Adults of both species adhere to clothes, feather and fur. Taeniopteryx nebulosa tarsomeres have many hooked setae, P. microcephalus tarsomeres have some hooked setae and a dense cover of microtrichia. They may disperse by hitchhiking on birds and mammals.     

Introgression and species demarcation in western European Leuctra fusca (Linnaeus, 1758) and L. digitata Kempny, 1899 (Plecoptera: Leuctridae)

The compilation of a DNA barcoding library of Norwegian stonefly (Plecoptera) species revealed that Leuctra fusca (Linnaeus, 1758 Linnaeus, C. (1758), Systema naturae Per Regna Tria Naturae: Secundum Classes, Ordines, Genera, Species, Cum Characteribus, Differentiis, Synonymis, Locis. Stockholm: Laurentius Salvius. [Google Scholar]) and Leuctra digitata Kempny, 1899 (Leuctridae) share haplotypes in northernmost Scandinavia. Phylogenetic analyses of the mitochondrial (mt) DNA barcode marker COI and the nuclear marker 28S show that the shared haplotypes must result from the introgression of a L. fusca mitochondrion into a L. digitata population on at least two occasions. Although mt introgression is widespread in animals, this represents the first documented case in Plecoptera. This study also included specimens of L. cf. fusca from the Sierra Nevada massif in Spain, a population previously known as L. carpentieri Despax, 1945. Their mt haplotypes are ca. 13% different from other European L. fusca. However, their 28S alleles are compatible with their morphological identification as L. fusca. In view of the possibility of mt introgression, the taxonomic status of this population remains undecided.     

Neotropical Osmylidae larvae (Insecta,Neuroptera): description of habitats and morphology

ABSTRACT

The larval stages of the genus Kempynus Navás, 1912 Navás, L. (1912), ‘Insectos neurópteros nuevos o poco conocidos’, Memorias de la Real Academia de Ciencias y Artes de Barcelona, 10, 135–202. [Google Scholar] (probably K. falcatus Navás, 1912 Navás, L. (1912), ‘Insectos neurópteros nuevos o poco conocidos’, Memorias de la Real Academia de Ciencias y Artes de Barcelona, 10, 135–202. [Google Scholar] based on the presence of synchronic and sympatric adults) are described for the Neotropical Region for the first time, and the larval stages of Isostenosmylus pulverulentus (Gerstaecker, 1893 Gerstaecker, C.E.A. (1893), ‘Ueber neue und weniger gekannte Neuropteren aus der familie Megaloptera Burm’, Mitt[h]eilungen aus dem Naturwissenschaftlichen Verein für Neu-Vorpommern und Rugen, 25, 93–173. [Google Scholar]) are redescribed. The external morphology of third-instar larvae of both species and their habitats are described and compared. Kempynus sp. is a water-dependent species and can be considered semi-aquatic, whereas I. pulverulentus larvae are terrestrial and live in undergrowth vegetation. The first key to identification of Neotropical Osmylidae larvae is provided, based on third-instar larvae of both species.     

The expression of aggression in the dobsonflies Corydalus magnus Contreras-Ramos, 1998 and Platyneuromus soror (Hagen, 1861) (Megaloptera: Corydalidae)

The expression of aggression in Megaloptera has received little attention, specifically for the adults of the subfamily Corydalinae. Among the New World species of Corydalinae, it is not known if aggression is triggered and expressed in the same way. Since two genera, Corydalus Latreille, 1802 Latreille, P.A. (1802), Histoire naturelle, générale et particulière des Crustacés et des Insectes. Ouvrage faisant suite aux ouvres de Leclerc Buffon et partie du cours complete d’Histoire naturelle rédigé par C.S. Sonnini, membre de plusieurs sociétés savantes. Vol. 3, Paris: F. Dufart. [Google Scholar] and Platyneuromus Weele, 1909 Weele, H.W. van der. (1909), ‘New Genera and Species of Megaloptera Latr.’, Notes from the Leyden Museum, 30, 249–253. [Google Scholar] have different courtship strategies, the effect of the social environment in the expression of aggression in two species of those genera, Corydalus magnus Contreras-Ramos, 1998 Contreras-Ramos, A. (1998), Systematics of the Dobsonfly genus Corydalus Latreille (Megaloptera: Corydalidae), Lanham, MD: Thomas Say Monographs, Entomological Society of America. [Google Scholar] and Platyneuromus soror (Hagen, 1861 Hagen, H.A. (1861), Synopsis of the Neuroptera of North America, with a List of the South American Species. Washington, DC: Smithsonian Institution.[Crossref] , [Google Scholar]), is examined here and compared with the known data in Corydalus bidenticulatus Contreras-Ramos, 1998 Contreras-Ramos, A. (1998), Systematics of the Dobsonfly genus Corydalus Latreille (Megaloptera: Corydalidae), Lanham, MD: Thomas Say Monographs, Entomological Society of America. [Google Scholar]. Our results suggest that the triggering of aggressive behaviours in the three species is similar. The decision of whether or not to fight is affected by their social environment: a male is aggressive against other males only when a female is present. Furthermore, the intensity of aggression does not differ among the three species. The behavioural observations support the idea that the mandibles of Corydalus males are used as weapons in male-male competition and during the courtship, but the post-ocular flanges of P. soror males are not involved in male-male competition (they use their short mandibles to bite). Conversely, data show that such a feature might act as a signal trait for female choice.     

Redescription of Potamolithus paranensis (Pilsbry, 1911) and Potamolithus simplex (Pilsbry, 1911) (Gastropoda: Tateidae)

Potamolithus Pilsbry &; Rush, 1896 is a species-rich genus, endemic to South America, with many of its species considered Vulnerable due to a restricted distribution; half of them are called into question, since they are known only from their shells. The purpose of this article is to describe the anatomy of P. paranensis (Pilsbry, 1911 Pilsbry, H.A. (1911) Non-marine Mollusca of Patagonia. In: Scott, W.B. (Ed.), Reports of the Princeton University Expeditions to Patagonia, 1896–1899, Vol 3, Zoology, Part V. The University, USA, Princeton, NJ, pp. 513–633. [Google Scholar]) and P. simplex (Pilsbry, 1911 Pilsbry, H.A. (1911) Non-marine Mollusca of Patagonia. In: Scott, W.B. (Ed.), Reports of the Princeton University Expeditions to Patagonia, 1896–1899, Vol 3, Zoology, Part V. The University, USA, Princeton, NJ, pp. 513–633. [Google Scholar]) from the Argentinean Misiones province, and to evaluate the value of anatomical features in this genus. These two species differ in penis morphology and pigmentation, ctenidium length, and relative position of the opening of the pallial oviduct, seminal receptacle and bursa copulatrix. Consequently, it appears that anatomical data could help solve taxonomic conflicts that are currently unresolved by shell morphology alone.     

Hydrotrupes chinensis Nilsson, 2003 (Coleoptera: Dytiscidae): new records, (re)description of adult and larva,and notes on its biology

Abstract

Hydrotrupes chinensis Nilsson, 2003 Nilsson, A.N. (2003), ‘Dytiscidae. XII. A New Species of Hydrotrupes Sharp from China, an Example of Pacific Intercontinental Disjunction (Coleoptera)’, in Water Beetles of China (Vol. 3), eds. M.A. Jäch and L. Ji, Vienna: Zoologische-Botanische, Gesellschaft, pp. 284–297. [Google Scholar] described from the holotype collected in Anhui Province, China, is newly recorded from three localities in Guangdong Province, ca. 750?km southwest from the type locality. The species seems to inhabit hygropetric habitats exclusively, with diurnal larvae and nocturnal adults hidden under stones or in cracks in rock during the day; when disturbed, the adults readily jumped off the rock surface. The adult is redescribed. The larvae are described and illustrated for the first time, with detailed morphometric and chaetotaxic analyses of the cephalic capsule, head appendages, legs, last abdominal segment, and urogomphi. Whereas similar morphologically to the Nearctic endemic Hydrotrupes palpalis Sharp, 1882 Sharp, D. (1882), ‘On Aquatic Carnivorous Coleoptera or Dytiscidae’, Scientific Transactions of the Royal Dublin Society, 2, 179–1003. [Google Scholar], the first instar larva of H. chinensis distinguishes by presence of six lamellae clypeales, two additional spine-like setae both on the last abdominal segment and urogomphomere 1, and the strongly developed egg bursters.     

A revision of fossil eagle owls (Aves: Strigiformes: Bubo) from Europe and the description of a new species,Bubo ibericus,from Cal Guardiola (NE Iberian Peninsula)

The European fossil record of eagle owls, genus Bubo Duméril 1806 Duméril AMC. 1806. Zoologie Analytique, ou Méthode Naturelle de Classification des Animaux, rendue plus Facile à l’Aide de Tableaux Synoptiques. Paris: H. L. Perronneau. [Google Scholar], is thought to extend back into the Miocene, but records of Bubo before the Middle Pleistocene are scarce and mainly constituted by non-diagnostic or fragmentary specimens. Apart from a number of fossil species of Bubo of uncertain validity, i.e. Bubo? florianae Kretzoi 1957 Kretzoi M. 1957. Bird remains from the Hipparion-fauna of Csákvár. Aquila. 63:239–248. [Google Scholar], Bubo lignitum Giebel 1860 Giebel CG. 1860. Zur Fauna der Braunkohlen Formation von Rippersroda in Thüringen. Zeitschrift für die Gesammten Naturwissenschaften. 16:147–153. [Google Scholar], and Bubo perpastus (Ballman 1976 Ballmann P. 1976. Fossile Vögel aus dem Neogen der Halbinsel Gargano (Italien). Zweiter Teil Scripta Geol. 38:1–59. [Google Scholar]), most fossil Bubo material is unassigned to species or assigned to the extant Bubo bubo (Linnaeus 1758) on the basis of size, especially for Early Pleistocene records. Given the ambiguity about the validity of the earliest records, here we revise the pre-Middle Pleistocene fossil record of Bubo in Europe. Our results indicate that, in Europe, Bubo is first recorded in the Late Pliocene/Early Pleistocene of Italy. By the Early Pleistocene, three taxa can be distinguished: Bubo ibericus sp. nov. from Cal Guardiola (Spain), Bubo sp. nov. indet. from Soave Cava Sud (Italy) and Bubo sp. from various sites across Europe. By the Middle Pleistocene, Eurasian environments experienced a substantial increase in severity and duration of glacial periods which might have led to the replacement of extinct species of Bubo by the recent B. bubo and Bubo scandiacus.     

An integrative approach underscores the taxonomic status of Lamellidens exolescens,a freshwater mussel from the Oriental tropics (Bivalvia: Unionidae)

The Oriental Region harbours the second richest fauna of freshwater bivalves in the world, including many endangered endemic taxa. However, the Oriental fauna of the Unionidae have been very poorly studied using an integrative taxonomic approach, which may provide reasonable revisions of complicated (cryptic) taxa based on morphological, molecular, biogeographic and ecological evidence. Here, we present the first example of an integrative taxonomic revision concerning the status of Unio exolescens Gould (1843 Gould, A.A. (1843). Dr. Gould had examined the shells not long since announced as having been received from the Rev. Francis Mason, missionary at Tavoy, in British Burmah. Proceedings of the Boston Society of Natural History, 1, 139–141. [Google Scholar]), a nominal mussel taxon that was accepted as a valid species within the genus Trapezoideus Simpson (1900). Currently, Trapezoideus exolescens is considered the type of the genus as far as the originally designated type species, U. foliaceus Gould (1843 Gould, A.A. (1843). Dr. Gould had examined the shells not long since announced as having been received from the Rev. Francis Mason, missionary at Tavoy, in British Burmah. Proceedings of the Boston Society of Natural History, 1, 139–141. [Google Scholar]), was considered to be a synonym of T. exolescens. Using nucleotide sequences obtained from mitochondrial (COI and 16S rRNA) and nuclear (28S rDNA) genes, we found that the topotypes of Unio exolescens Gould (1843 Gould, A.A. (1843). Dr. Gould had examined the shells not long since announced as having been received from the Rev. Francis Mason, missionary at Tavoy, in British Burmah. Proceedings of the Boston Society of Natural History, 1, 139–141. [Google Scholar]) cluster together with representatives of another mussel genus, Lamellidens Simpson (1900). Based on these results and on morphological data, we transfer Unio exolescens Gould (1843 Gould, A.A. (1843). Dr. Gould had examined the shells not long since announced as having been received from the Rev. Francis Mason, missionary at Tavoy, in British Burmah. Proceedings of the Boston Society of Natural History, 1, 139–141. [Google Scholar]) from Trapezoideus to Lamellidens and propose Lamellidens exolescens (Gould, 1843 Gould, A.A. (1843). Dr. Gould had examined the shells not long since announced as having been received from the Rev. Francis Mason, missionary at Tavoy, in British Burmah. Proceedings of the Boston Society of Natural History, 1, 139–141. [Google Scholar]) comb. nov. In addition, we revisited the status of Unio foliaceus Gould (1843 Gould, A.A. (1843). Dr. Gould had examined the shells not long since announced as having been received from the Rev. Francis Mason, missionary at Tavoy, in British Burmah. Proceedings of the Boston Society of Natural History, 1, 139–141. [Google Scholar]) as a valid species and the type of the genus Trapezoideus based on the morphological study of the type specimen, although a question concerning the true position of this taxon is still open because its molecular sequences are not available. Our findings highlight that an integrative taxonomic approach is an important tool, particularly when dealing with such species-rich Unionidae fauna as those of the Oriental Realm.     

A new species of Larsia Fittkau, 1962 (Diptera: Chironomidae: Tanypodinae) from phytotelmata of Aechmea distichantha Lemaire, 1853 (Bromeliaceae) in Argentina

A new species of Larsia Fittkau, 1962 Fittkau, E.J. (1962), ‘Die Tanypodinae (Diptera: Chironomidae) (Die Tribus Anatopyniini, Macropelopiini und Pentaneurini)’, Abhandlungen zur Larvalsystematik der Insekten, 6, 1–453. [Google Scholar], viz. Larsia angusticornis sp. n., is described and adults and immatures are figured. The study is based on larvae collected from phytotelmata of the bromeliad Aechmea distichantha Lemaire, 1853 Lemaire, A.C. (1853), Le Jardin Fleuriste; Journal General des Progres et des Interets Horticoles et Botaniques, 3: pl. 269. [Google Scholar] in northeastern Argentina that were reared to the adult stage. The pupa bears thoracic horns unusual for the genus, which distinguish this new species from other Larsia species.

http://zoobank.org/urn:lsid:zoobank.org:pub:41DFD96D-98E2-4FFC-9CDE-C290BCA84D45     

New records of Hydrochus Leach, 1817 (Coleoptera: Hydrochidae) from Iran

Abstract

Hydrochus ignicollis Motschulsky, 1860 Motschulsky, V. de (1860), ‘Coléoptères rapportés de la Sibérie orientale et notamment des pays situés sur les bords du fleuve Amour par MM. Schrenck, Maack, Ditmar, Voznessenski etc.’, in Reisen und Forschungen im Amur - Lande in den Jahren 1854–1856 im Auftrage der Kaiserl. Akademie der Wissenschaften zu St. Petersburg ausgeführt und in Verbindung mit mehreren Gelehrten herausgegeben. Band II. ed. L. Schrenck , Zweite Lieferung . Coleopteren, St. Petersburg: Eggers und Comp., pp. 80–257, pls. VI–XI. [Google Scholar] is recorded from Iran (Gilan Province) for the first time. In addition, new Iranian provincial records are provided for two species: H. nodulifer Reitter, 1897 Reitter, E . (1897), ‘Dreißig neue Coleopteren aus russisch Asien und der Mongolei’, Deutsche Entomologische Zeitschrift , 1897(2), 209–228. [Google Scholar] (Zanjan Province) and H. farsicus Hidalgo-Galiana, Jäch, and Ribera, 2010 Hidalgo-Galiana, A. , Jäch, M.A. , and Ribera, I . (2010), ‘ Hydrochus farsicus sp. n. from Iran and Notes on other Palearctic Species of the Genus (Coleoptera: Hydrophiloidea: Hydrochidae)’, Zootaxa , 2344, 61–64.[Crossref] , [Google Scholar] (Kohgiluyeh and Boyer-Ahmad Province). Photographs of the habitus, the male genitalia and the habitat of H. ignicollis are provided.     

Taxonomic notes about Paropta Staudinger, 1899 (Lepidoptera: Cossidae)

In this study we allocate lectotypes for Cossus l-nigrum Bethune-Baker, 1894, Paropta pharaonis Bang-Haas, 1910 and Cossus frater Warnecke, 1929. New synonymies are established: Paropta Staudinger, 1899 = Alcterogystia Schoorl, 1990 Schoorl, J. W. (1990): A phylogenetic study on Cossidae (Lepidoptera: Ditrysia) based on external adult morphology. Zoologische Verhandelingen, 263, 3–295. [Google Scholar], syn. n.; Cossus lnigrum Bethune-Baker, 1894 = Paropta paradoxus (Herrich-Schäffer, [1851]), syn. n.; Paropta pharaonis Bang-Haas, 1910 = Paropta paradoxus (Herrich-Schäffer, [1851]), syn. n. It has been proved that Cossus frater Warnecke, 1929 belongs to the genus Paropta Staudinger, 1899.     

A new species of Pelomus Reiss, 1989 (Diptera: Chironomidae: Chironominae) from the Neotropical Region,with emendation of the generic diagnosis

A new species of Pelomus Reiss, 1989 Reiss, F. 1989. ‘Pelomus gen. nov., ein weiterer potamobionter Vertreter des Harnischia-Komplexes aus dem Amazonasbecken (Diptera, Chironomidae)’. Acta Biologica Debrecina Oecologia Hungarica, 2: 305–314.  [Google Scholar] (Diptera: Chironomidae: Chironominae), P. sophiae sp. n., is described and figured as male, pupa and larva. Diagnoses for male and pupa of the genus are emended. The larvae, reared in the laboratory to obtain all life stages, were collected on bottom sand of reservoir and ponds, in southeast Brazil.     

Chironomidae (Insecta: Diptera) from four protected areas in the state of Pernambuco,Brazil

New records and distributional notes of Chironomidae (Insecta, Diptera) are provided for four protected areas in the state of Pernambuco, northeastern Brazil. Additionally, we also present new records and update of distributional ranges from Brazil and the Neotropical Region. In total, 810 specimens belonging to 35 genera within the subfamilies Chironominae (22 taxa), Tanypodinae (11 taxa) and Orthocladiinae (2 taxa) were found. The subfamilies Chironominae and Tanypodinae predominated. Axarus Roback, 1980 Roback, S.S. (1980), ‘New name for Anceus Roback nec Anceus Risso’, Entomological News, 91, 32.[Web of Science ®] , [Google Scholar] and the Tanytarsus ortoni-group were recorded for the first time in the state of Pernambuco, while Nanocladius Kieffer, 1913a Kieffer, J.J. (1913b), ‘Nouvelle étude sur les Chironomides de l'Indian Museum de Calcutta’, Records of the Indian Museum, 9, 119–197. [Google Scholar] was recorded for the first time in the Northeast Region of Brazil. Our results make evident how much and where current knowledge of the northeastern Brazil chironomids remains fragmentary.     

The altitudinal limit of Leptohyphes Eaton, 1882 and Lachlania Hagen, 1868 (Ephemeroptera: Leptohyphidae,Oligoneuriidae) in Ecuadorian Andes streams: searching for mechanisms

We explored mechanisms determining the upper altitudinal limit of ephemeropterans from two different genera: Leptohyphes Eaton, 1882 Eaton, A.E. (1882), ?An Announcement of New Genera of the Ephemeridae?, The Entomologist's Monthly Magazine, 18, 207–208. [Google Scholar] (Leptohyphidae) and Lachlania Hagen, 1868 Hagen, H.A. (1868), ?On Lachlania Abnormis: A New Genus and Species from Cuba Belonging to the Ephemerina?, Proceedings of the Boston Society of Natural History, 11, 372–375. [Google Scholar] (Oligoneuriidae). For this, we (1) surveyed the two taxa in 165 stream sites along a wide altitudinal gradient; (2) sampled benthic fauna at short altitudinal intervals along a stream, from 2780 to 3150 m above sea level; (3) collected adults at the lowest and highest sites; and (4) transplanted nymphs from the lowest to the highest study site in our stream to determine survival over time. Densities of the two taxa declined gradually with altitude and both disappeared between 2950 and 3080 m a.s.l. The upper altitudinal limit in the stream seemed to be most closely related to mean oxygen saturation, temperature, and current velocity. Adults were collected where the nymphs were found, but not at the upstream site where the nymphs were absent, implying limited upstream dispersal of adults and some of the altitudinal constraint lying at the adult stage. Short-term survival of transplanted nymphs was lower than that of controls, suggesting that the distribution was limited at the juvenile stage, and that at least some of the altitudinal constraint is related to the abiotic stream environment.     

A new clionaid sponge infests live corals on the west coast of India (Porifera,Demospongiae, Clionaida)

Coral reef ecosystems depend on the balanced interplay of constructive and destructive processes and are increasingly threatened by environmental change. In this context bioeroding sponges play a significant role in carbonate cycling and sediment production. They occasionally aggravate erosional processes on disturbed reefs. Like other coral ecosystems, Indian reefs have suffered from local and global effects. However, the systematic affiliation and diversity of many Indian bioeroding sponges and their infestation rates are largely confused or unknown. The present study describes a new bioeroding sponge species, Cliona thomasi sp. nov. from the central west coast of India. It belongs to the Cliona viridis species complex, displaying the key characters of tylostyles and spirasters, as well as harbouring photosymbiotic dinoflagellates. Specific morphological characteristics and molecular data from nrITS1 DNA and 28S rDNA distinguished C. thomasi sp. nov. from other known C. viridis complex and a number of Spheciospongia species. The historic sample of ‘Suberites coronarius’ from Mergui Archipelago (sensu Carter, 1887 Carter, H. J. (1887). Report on the marine sponges, chiefly from King Island, in the Mergui Archipelago, collected for the trustees of the Indian museum, Calcutta, by Dr. John Anderson, F. R. S., superintendent of the museum. Zoological Journal of the Linnean Society, 21, 61–84. https://doi.org/10.1111/j.1096-3642.1887.tb00381.x[Crossref] , [Google Scholar]), but not from the Caribbean (sensu Carter, 1882 Carter, H. J. (1882). Some sponges from the West Indies and Acapulco, in the Liverpool Free Museum, described with general and classificatory remarks. Annals and Magazine of Natural History, 9, 266–301, 346–368, pls. XI-XII. https://doi.org/10.1080/00222938209459039[Taylor &; Francis Online] , [Google Scholar]), is conspecific with C. thomasi sp. nov. Cliona thomasi sp. nov. is locally very abundant, appears to be a key bioeroder, and thus regular monitoring of its abundance, distribution and infestation patterns is recommended.     

First description of hatchlings and eggs of Octopus oliveri (Berry, 1914) (Cephalopoda: Octopodidae)

Chromatophore patterns can be used to identify paralarvae at the species level and are used here to distinguish Octopus oliveri (Berry, 1914 Berry, S. (1914) Notes on the collection of cephalopods from the Kermadec Islands. Transactions of the New Zealand Institute 46, 134–149. [Google Scholar]) from other Hawaiian cephalopod paralarvae. Eggs, clutches, and hatchlings are described for the first time in O. oliveri. Preservation times are compared to illustrate variation in founder chromatophore patterns even among individuals of the same brood.