A Third Species of Hemilecanium Newstead (Hemiptera: Coccoidea: Coccidae) from the New World, with Keys to Species in the Genus

A new species of Hemilecanium Newstead, Hemilecanium guanabana Kondo & Hodgson n. sp., is described and illustrated based on the adult female, adult male and first instar. The specimens were collected in the municipality of Palmira, state of Valle del Cauca, Colombia, on soursop, Annona muricata (Annonaceae). Updated identification keys are provided for the adult females of all 28 species of the genus Hemilecanium, and for known adult males and first instars. An updated list of the 23 species of soft scales (Coccidae) known from soursop worldwide is included.     

Host stage selection of the mealybug parasitoid Anagyrus spec. nov near sinope

The mealybug parasitoid Anagyrus spec. nov near sinope (Hymenoptera: Encyrtidae) is an undescribed parasitoid of the Madeira mealybug, Phenacoccus madeirensis Green (Homoptera: Pseudococcidae). We investigated the preference of Anagyrus spec. nov near sinope for six developmental stadia (first‐ and second‐instar nymphs, third‐instar immature females, third‐ or fourth‐instar immature males, pre‐reproductive adult females, and ovipositing adult females) of P. madeirensis and the fitness consequences of the host stage selection behavior. In the no‐choice test, Anagyrus spec. nov near sinope parasitized and completed development in all host stadia except third‐instar immature males. When all host stadia were offered simultaneously, the parasitoids preferred third‐instar immature and pre‐reproductive adult females. Dissection of the stung mealybugs revealed that the clutch size (number of eggs per host) was approximately four and three in the third‐instar and pre‐reproductive females, respectively, and one egg per first‐instar nymph. Parasitoids emerged from P. madeirensis parasitized at third‐instar or pre‐reproductive adult female completed development in the shortest duration, achieved a higher progeny survival rate, larger brood and body size, and the lowest proportion of males. We showed that the continued development of mealybugs had significant influence on the fitness of the parasitoids. Although deposited as eggs in first‐ or second‐instar nymphs, parasitoids emerged from mummies that had attained third‐instar or adult development achieved similar progeny survival rate, brood size, body size, and sex ratio as those parasitoids deposited and developed in third‐instar or adult mealybugs. By delaying larval development in young mealybugs, Anagyrus spec. nov near sinope achieved higher fitness by allowing the parasitized mealybugs to grow and accumulate body size and resources. We suggest that the fitness consequence of host stage selection of a koinobiont parasitoid should be evaluated on both the time of parasitism and the time of mummification.     

INDIAN OCEAN NANNOPLANKTON. II. HOLOCOCCOLITHOPHORIDS (CALYPTROSPHAERACEAE,PRYMNESIOPHYCEAE) WITH A REVIEW OF EXTANT GENERA1

Holococcolithophorids, pyrmnesiophytes having only one type of calcareous element in their coccoliths, are delicate and not commonly recorded in recent and fossil marine floras. There are few records of these organisms from the Indian Ocean and 26 species from there are included in this report. Although the group, generally assigned to a single family, the Calyptrosphaeraceae, may contain species that are part of the life history of heterococcolith-bearing cells in other stages, so little is known of this aspect of their biology that one must continue, at the present time, to treat them as independent taxonomic entities. A key is provided for the known holococcolithophorid genera. A new genus, Gliscolithus, and three new species, Gliscolithus amitakarenae, Calyptrosphaera heimdalae, and Helladosphaera pienaarii are described. The following new combinations are proposed: Calyptrolithina fragaria (Kamptner) comb. nov., Calyptrolithina gaarderae (Borsetti et Cati) comb. nov., Calyptrolithina isselii (Borsetti et Cati) comb. nov., Calyptrolithina lafourcadii (Lecal) comb. nov., Calyptrolithina magnaghii (Borsetti et Cati) comb. nov., Calyptrolithina multipora (Gaarder) comb. nov., Calyptrolithina porritectum (Heimdal) comb. nov., Calyptrolithina wettsteinii (Kamptner) comb. nov., Calyptrolithophora catillifera (Kamptner) comb. nov., Calyptrolithophora galea (Lecal-Schlauder) comb. nov., Dactylethra pirus (Kamptner) comb. nov., Helladosphaera arethusae (Kamptner) comb. nov., Helladosphaera gracilis (Kamptner) comb. nov., Homozygosphaera strigilis (Gaarder) comb. nov. and Syracolithus schilleri (Kamptner) comb. nov. The new combination in the genus Dactylethra Gartner for the first time brings an extant species into this genus that formerly contained only fossil species. It is pointed out that the enlarged zygoliths in stomatal areas of Corisphaera and the helladoliths in stomatal regions of Helladosphaera have intergrading types and are not distinctive enough characteristics to separate these genera.     

Notes on marine algae from Hateruma island,Ryukyu

This paper deals with a small collection of marine algae which the author gathered at Hateruma island, one of the southernmost islands of the Ryukyu groups. Twelve species are reported; seven of which,Udotea glaucescens, Codium ovale, Halimeda micronesica, H. fragilis, Ectocarpus laurenciae, Centroceras apiculatum andCeramium sympodiale, are recorded here for the first time in Japan, one of which,Feldmannia formosana, is proposed as comb. nov., the other four,Chlorodesmis haterumana, Struvea haterumensis, Centroceras japonicum andLophocladia minima, are described here as new species.     

Molecular data reveal convergent reproductive strategies in iceryine scale insects (Hemiptera: Coccoidea: Monophlebidae), allowing the re-interpretation of morphology and a revised generic classification

Abstract The scale insect tribe Iceryini (Coccoidea: Monophlebidae) is a group of relatively large and polyphagous insects found worldwide. Currently, the tribe contains about 80 named species placed in seven genera, which are diagnosed largely on features associated with egg protection. We reconstruct the phylogeny of the Iceryini on the basis of nucleotide sequence data from nuclear ribosomal (18S and D2, D3 and D10 regions of 28S) and protein‐coding (histone H3) gene regions of 40 iceryine species representing six of the seven genera and seven outgroup taxa, mostly from two other tribes of Monophlebidae. Bayesian and maximum parsimony analyses recover a monophyletic tribe and clades that correspond more to geography than to the existing morphology‐based classification. Gueriniella Fernald is sister to the rest of the Iceryini and the genera Crypticerya Cockerell, Icerya Signoret and Steatococcus Ferris are not monophyletic. Our data imply that the distinctive iceryine reproductive strategies, such as protecting eggs in a waxy ovisac or inside a marsupium, are poor indicators of relationships. On the basis of molecular relationships and the re‐examination of morphological characters, we recognize only five genera of Iceryini –Crypticerya, Echinicerya Morrison, Gigantococcus Pesson & Bielenin, Gueriniella and Icerya – and substantially revise the generic concepts of Crypticerya, Gigantococcus and Icerya. We provide a key to the genera based on adult females. We redescribe and illustrate the adult female and first‐instar nymph of the type species Crypticerya rosae (Riley & Howard), Echinicerya anomala Morrison, Gigantococcus maximus (Newstead) (adult female only), Gueriniella serratulae (Fabricius) and Icerya seychellarum (Westwood). We recognize Auloicerya Morrison as a junior synonym ( syn.n. ) of Icerya, and transfer the two Auloicerya species to Icerya as I. acaciae (Morrison & Morrison) comb.n. and I. australis Maskell comb.rev. We recognize Steatococcus and Proticerya Cockerell as junior synonyms ( syn.n. ) of Crypticerya. From Steatococcus, we transfer five species to Crypticerya [C. mexicana Cockerell & Parrott comb.rev. , C. morrilli (Cockerell) comb.n. , C. tabernicola (Ferris) comb.n. , C. townsendi Cockerell comb.rev. , C. tuberculata (Morrison) comb.n. ], four species to Gigantococcus [Gi. euphorbiae (Brain) comb.n. , Gi. gowdeyi (Newstead) comb.n. , Gi. madagascariensis (Mamet) comb.n. , Gi. theobromae (Newstead) comb.n. ] and three species to Icerya [I. assamensis (Rao) comb.n. , I nudata Maskell comb.rev. , I. samaraia (Morrison) comb.n. ]. From Icerya, we transfer 14 species to Crypticerya [C. brasiliensis (Hempel) comb.n. , C. colimensis (Cockerell) comb.n. , C. flava (Hempel) comb.n. , C. flocculosa (Hempel) comb.n. , C. genistae (Hempel) comb.n. , C. littoralis (Cockerell) comb.n. , C. luederwaldti (Hempel) comb.n. , C. minima (Morrison) comb.n. , C. montserratensis (Riley & Howard) comb.n. , C. palmeri (Riley & Howard) comb.n. , C. rileyi (Cockerell) comb.n. , C. similis (Morrison) comb.n. , C. subandina (Leonardi) comb.n. , C. zeteki (Cockerell) comb.n. ] and nine species to Gigantococcus [Gi. alboluteus (Cockerell) comb.n. , Gi. bimaculatus (De Lotto) comb.n. , Gi. brachystegiae (Hall) comb.n. , Gi. longisetosus (Newstead) comb.n. , Gi. nigroareolatus (Newstead) comb.n. , Gi. pattersoni (Newstead) comb.n. , Gi. schoutedeni (Vayssière) comb.n. , Gi. splendidus (Lindinger) comb.n. , Gi. sulfureus (Lindinger) comb.n. ]. From Crypticerya, we transfer seven species to Icerya [I. clauseni (Rao) comb.n. , I. jacobsoni Green comb.rev. , I. jaihind (Rao) comb.n. , I. kumari (Rao) comb.n. , I. mangiferae (Tang & Hao) comb.n. , I. natalensis (Douglas) comb.rev. , I. nuda Green comb.rev. ] and five species to Gigantococcus [Gi. bicolor (Newstead) comb.n. , Gi. cajani (Newstead) comb.n. , Gi. caudatus (Newstead) comb.n. , Gi. ewarti (Newstead) comb.n. , Gi. rodriguesi (Castel‐Branco) comb.n. ]. Both I. hyperici (Froggatt) and Palaeococcus dymocki (Froggatt) are syn.n. of I. nudata (all previously placed in Steatococcus). We recognize I. maynei Vayssière as a syn.n. of Gi. nigroareolatus, I. tremae Vayssière as a syn.n. of Gi. schoutedeni and I. townsendi plucheae Cockerell as a syn.n. of C. townsendi. We revalidate the species name I. crocea Green stat.reval. In addition, we transfer I. taunayi Hempel to Laurencella Foldi (Monophlebidae: Llaveiini) as L. taunayi (Hempel) comb.n. Four species, Coccus hirticornis Boyer de Fonscolombe, I. chilensis Hempel, I. insulans Hempel and I. paulista Hempel, are considered incertae sedis. We designate lectotypes for C. rosae, E. anomala and I. candida (a junior synonym of I. seychellarum). Following this revision, we recognize 74 species of Iceryini, distributed as follows: 22 in Crypticerya, one in Echinicerya, 19 in Gigantococcus, two in Gueriniella and 30 in Icerya.     

A new species of the genus Molanna Curtis (Trichoptera, Molannidae) from the Yaeyama Islands, the southernmost part of Japan

A new species of molannid caddisfly, Molanna yaeyamensis sp. nov., is described based on adult and immature stages from the Yaeyama Islands, the Ryukyu Archipelago, the southernmost part of Japan.     

Oviposition behaviour, influence of experience on host size selection, and niche overlap of the solitary Leptomastix epona and the gregarious Pseudaphycus flavidulus, two endoparasitoids of the mealybug Pseudococcus viburni

Oviposition behaviour and host size selection of the solitary parasitoid Leptomastix epona(Walker) and the gregarious Pseudaphycus flavidulus(Brèthes) [both Hymenoptera: Encyrtidae] were examined on five size classes of the mealybug Pseudococcus viburni(Signoret) [Hemiptera: Pseudococcidae]. The host size classes mostly consisted of one stage (first, second, third instar nymph, young adult and preovipositing adult) and were presented together to wasps of either parasitoid species. Both parasitoid species locate the host by drumming the surface of the patch with the antennae. Leptomastix eponaseems to use mainly the antennae to examine the host but P. flavidulusmay accept or reject a host for oviposition after antennation or insertion of the ovipositor. Leptomastix eponaattempts oviposition in all the host stages from second instar nymphs but P. flavidulusincludes first instar. Both parasitoid species select mainly larger hosts (>1 mm, third instar nymphs) to oviposit but P. flavidulusis able to parasitize more second instar nymphs compared to L. epona. Female wasps of L. eponamay host feed on small mealybugs (second and third instar nymphs) that they do not use for oviposition. Oviposition experience of either parasitoid species for 24 hours does not influence host size selection on patches with hosts of similar mixed sizes. Oviposition decisions are independent of the host sizes of the preceding ovipositions. Implications about stability of a single parasitoid – host system and the success of biological control of the mealybug were discussed in respect of the developmental refugia of the two parasitoid species. Niche overlap of the two parasitoid species was discussed with a view to giving an insight into a single or multiple introduction.     

Free‐living calamyzin chrysopetalids (Annelida) from methane seeps,anoxic basins,and whale falls

Members of Calamyzinae, a clade of free‐living and ectoparasitic chrysopetalids, are mainly associated with deep‐sea chemosynthetic environments. The three currently known free‐living calamyzin species are placed in Vigtorniella. A new free‐living calamyzin species similar to these is described here. Phylogenetic analyses of Calamyzinae using mitochondrial (cytochrome c oxidase subunit I and 16S rDNA) and nuclear (Histone H3 and 18S rDNA) loci showed that Vigtorniella and the new species form a grade with respect to an ectoparasitic clade, requiring two new genera to be erected. All free‐living calamyzins show a similar anterior end and chaetal morphology. Micospina auribohnorum gen. et sp. nov. is described for the small‐bodied new species from deep‐sea whale falls off California and methane seeps off Costa Rica. The maximum‐likelihood and Bayesian analyses show Micospina gen. nov. as sister to the ectoparasitic clade. Boudemos gen. nov. is named for the clade of two larger‐bodied species: Boudemos flokati gen. et comb. nov. and Boudemos ardabilia gen. et comb. nov., which is sister group to all other Calamyzinae. Vigtorniella is retained for the type species, Vigtorniella zaikai (Kiseleva, 1992), with the adults found amongst bacterial mats at the boundary of the hydrogen sulphide zone in the Black Sea. Micospina gen. nov., Boudemos gen. nov., and Vigtorniella form a grade of free‐living taxa that is associated with feeding on organic‐enriched sediments, and the latter two taxa display ontogenetic jaw change. Jaws are absent in Micospina auribohnorum gen. et sp. nov. and most of the calamyzin clade of parasitic forms.