Showing posts with label Entomology. Show all posts
Showing posts with label Entomology. Show all posts

Wednesday, June 25, 2025

[Paleontology • 2025] Paleoophiocordyceps gerontoformicae & P. ironomyiae • Cretaceous Entomopathogenic Fungi illuminate the early Evolution of Insect–fungal Associations


An Cretaceous ant carries a fungus-infected ant pupa 

in Zhuang, Luo, Tang, Araújo, Yu, Zhao, Haelewaters, Nyunt, Zhang, Jarzembowski, Meng, Ran, Liu et Wang, 2025. 
artwork by Dinghua Yang



Abstract
Throughout evolution, entomopathogenic (insect-pathogenic) fungi have played a pivotal role in regulating insect populations. However, little is known about ancient entomopathogenic fungi due to the scarcity of fossils displaying typical pathogenic structures on their presumed hosts. Here, we report two new fungi, Paleoophiocordyceps gerontoformicae sp. nov. and Paleoophiocordyceps ironomyiae sp. nov., from mid-Cretaceous Kachin amber (approx. 99 million years old). They share common traits with Ophiocordyceps and are associated with an ant pupa and a fly, respectively. These fossils are among the oldest fossil records of animal-pathogenic fungi. In addition, we performed a divergence time estimation analysis showing that Ophiocordyceps likely originated during the Early Cretaceous. We further compiled the hosts of extant Ophiocordyceps and inferred the evolution of host associations within the genus based on ancestral character state reconstruction. Our results suggest that Ophiocordyceps made a host jump from Coleoptera to Lepidoptera and Hymenoptera during the Cretaceous, and its subsequent speciation was probably related to the increase in diversity and abundance of its moth and ant hosts. Our results not only highlight the ecological significance of pathogenic fungi in Mesozoic terrestrial ecosystems, but also provide new insights into the coevolution between entomopathogenic fungi and host insects.

Keywords: fossil, Mesozoic, host–parasite association, ant, amber



 Paleoophiocordyceps gerontoformicae sp. nov. 
 Paleoophiocordyceps ironomyiae sp. nov.



Yuhui Zhuang, Cihang Luo, Dexiang Tang, João Paulo Machado de Araújo, Hong Yu, Jing Zhao, Danny Haelewaters, Thet Tin Nyunt, Qingqing Zhang, Edmund A. Jarzembowski, Guoliang Meng, Hao Ran, Yu Liu and Bo Wang. 2025. Cretaceous Entomopathogenic Fungi illuminate the early Evolution of Insect–fungal Associations. Proc. R. Soc. B. 292; 20250407. DOI: doi.org/10.1098/rspb.2025.0407 [11 June 2025]  
https://www.sciencenews.org/article/zombie-fungi-infecting-ants-fossil
https://www.nhm.ac.uk/discover/news/2025/june/origins-of-parasitic-fungi-that-inspired-the-last-of-us-revealed.html

Wednesday, December 4, 2019

[Entomology • 2019] Melanosphecia paolo • A New Species of Spectacular Spider Wasp Mimic Moth (Lepidoptera: Sesiidae: Osminiini) from Thailand is the First Representative of the Genus Melanosphecia Le Cerf 1916 to be filmed in the Wild


Melanosphecia paolo Skowron Volponi

in Skowron Volponi, 2019.

Abstract
A metallic blue, new species of clearwing moth from Thailand is described and shown on video. With its spectacular colouration, long hind legs and an incredible illusion of a wasp-waist, complemented by behavioural imitations, this sesiid is a striking spider wasp mimic. Notes on possible mimicry models, behaviour and conditions of occurrence are given. COI DNA barcode sequence is provided. This is the first country record of Melanosphecia Le Cerf 1916 for Thailand and the first representative of this genus to be filmed in its natural habitat.

Keywords: Lepidoptera, clearwing moth, mimicry, behaviour, mud-puddling, Hymenoptera, Pompilidae, Southeast Asia, barcoding


Melanosphecia paolo Skowron Volponi sp. nov.

Etymology. I dedicate this species to my husband, Paolo Volponi, a brilliant filmmaker and clearwing moth enthusiast, whose help and assistance in the field have been crucial in the studies of this and many other Sesiidae species.


Marta A. Skowron Volponi. 2019. A New Species of Spectacular Spider Wasp Mimic Moth from Thailand is the First Representative of the Genus Melanosphecia Le Cerf 1916 (Lepidoptera: Sesiidae: Osminiini) to be filmed in the Wild. Zootaxa. 4695(3); 295–300. DOI: 10.11646/zootaxa.4695.3.4

Thursday, October 31, 2019

[Entomology • 2019] Taxonomic Review and Distribution of the Genus Vespula Thomson, 1869 (Hymenoptera: Vespidae: Vespinae) from Vietnam


Vespula orbata (Buysson, 1902)

in Nguyen, Vu, et al., 2019.

Abstract
A taxonomic review of the genus Vespula Thomson in Vietnam is reported. Three species are recorded: V. flaviceps (Smith, 1870), V. koreensis (Radoszkowski, 1887), and V. orbata (Buysson, 1902). Of these, V. flaviceps is newly recorded from Vietnam. Distribution records of all three species and an identification key to species based on morphological characters are presented. Vespula koreensis is distributed from high (Cao Bang, Vinh Phuc, Quang Tri) to lower areas (Thai Nguyen, Tuyen Quang, Lang Son, Bac Giang), while the other two species are distributed in high mountainous areas of the northern and central regions of Vietnam such as in Cao Bang, Lao Cai, Son La, Phu Tho, Vinh Phuc, Quang Tri and Quang Nam provinces.

Keywords: Hymenoptera, Social Wasps, Yellow Jackets, Vespula, Taxonomy, Vietnam


Vespula orbata (Buysson, 1902) 


Lien Thi Phuong Nguyen, Thuong Thi Vu, Anthony Daglio and Bogdan Wiśniowski. 2019. Taxonomic Review and Distribution of the Genus Vespula Thomson, 1869 (Hymenoptera: Vespidae: Vespinae) from Vietnam. Zootaxa. 4691(3); 279–285. DOI:  10.11646/zootaxa.4691.3.8

Saturday, October 26, 2019

[Entomology • 2019] Gynacantha vargasi • A New Species of Dragonfly (Odonata: Anisoptera: Aeshnidae) from Costa Rica


Gynacantha vargasi Haber, 2019


Abstract 
The male and female of Gynacantha vargasi sp. nov. are described from three sites on the Caribbean slope of Costa Rica. The species is distinguished from its congeners by lime-green lateral thoracic stripes, orange-brown hind femur tipped with black, dorsal side of the hind tibia yellow, unique cercus shape, diurnal behavior, and barcode analysis. A key to all species of Gynacantha recorded from Mexico and Central America is provided.

Keywords: Odonata, barcode, dragonflies, endangered species, endemic, darners, Gynacantha caudataGynacantha tenuis, key to species, Monteverde

Gynacantha vargasi sp. nov., holotype male.

Gynacantha vargasi sp. nov.

Etymology. This species is named in honor of Ronald Vargas Castro, one of Costa Rica’s great naturalists, a trusted companion who has accompanied me on many Odonata expeditions in Costa Rica and Ecuador and who has collected numerous rare and undescribed species of Odonata, including two of the four known specimens of this new Gynacantha.


William A. Haber. 2019. Gynacantha vargasi (Odonata: Anisoptera: Aeshnidae) sp. nov. from Costa Rica. Zootaxa. 4612(1); 58–70. DOI: 10.11646/zootaxa.4612.1.3

Abstract: El macho y la hembra de Gynacantha vargasi sp. nov. se describen de tres sitios en la vertiente caribeña de Costa Rica. La especie se distingue de sus congéneres por sus franjas torácicas laterales de color verde limón, el fémur posterior de color marrón anaranjado con el ápice negro, lado dorsal de la tibia trasera amarillo, la forma única del cerco, su comportamiento diurno, y el análisis de código de barras. Se proporciona una clave para todas las especies de Gynacantha registradas de México y América Central.

Friday, October 18, 2019

[Entomology • 2019] Vespamantoida wherleyi • A Novel Form of Wasp Mimicry in A New Species of Praying Mantis (Mantodea, Mantoididae) from the Amazon Rainforest


 Vespamantoida wherleyi 
Svenson & Rodrigues, 2019


Abstract 
A wasp mimicking praying mantis (Mantodea) of the early evolving Mantoididae family was discovered in 2013 at a research station near the Amazon River in Northern Peru. This adult specimen exhibited a striking bright red/orange and black coloration pattern that was undocumented in all known praying mantis species. We tested the status of this new specimen using external morphology, male genital dissections, and geographic distribution. Our findings demonstrate the specimen to represent a new species, Vespamantoida wherleyi gen. nov. sp. nov., that is closely allied with a recently described species, Mantoida toulgoeti Roy, 2010, both of which are included within the newly erected genus. To support our actions, we present high resolution images of museum preserved and living specimens, morphological illustrations, a generic-level distribution map, and recorded video of the behavior of the holotype taken in the field at the time of collection. The bright red/orange coloration contrasted with black markings, the general appearance of a hymenopteran that includes a narrowed wasp waist, and the locomotory patterns and antennal movements mark this newly discovered species as unique among all hymenopteran mimicking Mantoididae as well as all other praying mantises.

Figure 1: Vespamantoida wherleyi gen. nov. sp. nov. male holotype from Peru, live habitus photos (CMNHENT0129976).
 (A) On twig; (B) on leaf. Photo credit: Gavin J. Svenson.
  


Vespamantoida gen. nov. 

Type-species— Vespamantoida wherleyi sp. nov. by original designation

Diagnosis— Forefemur narrow basally, only slightly wider than apex; discoidal spines elevated well above the ventral plane on a pronounced discoidal swelling (Figs. 4A–4D). Anteroventral femoral spines loosely arranged in two rows of three spines followed by a single row of four spines (Figs. 4A and 4B). Distal half of the first segment of the foretarsi flattened, laterally expanded, and black, forming a tarsal paddle (Figs. 4A–4D). Distal process of the ventral phallomere densely setose from narrowly rounded terminus to a heavily sclerotized, broad base; process comprised entirely of the paa, the distal process (pda) is highly reduced or absent (Figs. 5C and 5D).

Distribution— Although species of Mantoida are recorded across a broad range from Florida, USA to Northern Argentina, both Paramantoida amazonica and both species of Vespamantoida are restricted. Paramantoida amazonica is only recorded from a long transect that roughly follows the northern boundary of the Rio Negro from Manaus to the Parque Nacional Serrania La Neblina in southern Venezuela. The two species of Vespamantoida are found far from each other on near opposite sides of the Amazon Basin. This extremely disjunct distribution is supportive of the distinct boundary between the two species.

Etymology— Vespamantoida from the Latin word vespa, meaning “wasp,” and Mantoida, the name of the type genus of the family Mantoididae. This is a reference to the striking similarity between the type species and wasps.


Vespamantoida toulgoeti (Roy, 2010)
Mantoida toulgoeti (Roy 2010; Agudelo 2014; Roy 2019)


Vespamantoida wherleyi sp. nov.

Type Locality—Peru, Loreto Province, Madre Selva Biological Research Station.

Diagnosis—Head is bright red/orange with symmetrical black markings on the anterior half of the vertex and the ocellar tubercle; the pronotum, thorax, and first three segments of the abdomen bright red/orange. The forelegs and mesothoracic legs orange. The metathoracic legs are orange in the proximal half of the femur, then black to reddish to the terminus of the tibiae; the tarsi are orange. The flagellum of the antennae of the male thickening from base to the broadest antennomers 7–9, then tapering thinner to the terminus. A dark black spot centrally located on the frontal sclerite. The L1 shaped as an elongated bar with a slight curve distally that orients towards the afa, to form a claw-like structure with a broadly open gap (Figs. 1, 2, 4B, 4D, 5D, 6C, 6D, 7B and 7D).

Comments— This species is distinct from V. toulgoeti in the coloration of the specimen, the shape of the antennae and the male genitalia. The distribution of the two species, V. toulgoeti only known from French Guiana and V. wherleyi only from Northern Peru, allows for easy diagnosis between the congeneric species. The female of V. wherleyi is currently unknown.

Distribution— Known only from the type locality on the southern bank of the Amazon River in Northern Peru (Fig. 8; Table S1). Sympatric species of Mantoida were sampled from the same location, but none exhibited coloration outside of dark brown and black that is typical for the genus.

Etymology— Named for Rick Wherley, a valued member of the systematic entomology group at Cleveland Museum of Natural History. He has enriched the scientific content of the Museum for many years through imaging and computational improvements.

Natural history— The type specimen was collected in dense, tropical rainforest near the banks of small tributary of the Amazon River in Northern Peru. The specimen flew to our sampling lights within an hour after dark and was taken from the sheet shortly after. No observations were made of the mantis in situ for fear it would fly away and not be found again. The specimen was placed in a small enclosure on natural vegetation taken from the surrounding habitat for observation. Short video clips were recorded of the mantis walking on a blunt stick within this placed vegetation (Video S1). The 19 second video, including two behavioral segments, clearly demonstrates a number of behavioral characteristics that are strikingly similar to the movement patterns of many hymenopteran wasps. First, the mantis walks forward, with the head in a lowered position, and rapidly sweeps side to side, rotating its body in an alternating, circuitous pattern as it moves forward. This pattern is broken up by larger redirections on the terminus of the stick in what appears to be a search behavior. A second similarity is the antennal movements beginning a rapid up and down pattern that appears to be contacting the substrate to feel or sense the environment while walking, then moving with a declining amplitude following a pause in walking. A third similarity is the slight up and down movement of the abdomen while walking that resembles a hymenopteran-like pumping or venting behavior. The fourth similarity is the rapidity of the mantis’ walking and the rapid start and stop to this motion.


Gavin J. Svenson and Henrique M. Rodrigues. 2019. A Novel Form of Wasp Mimicry in A New Species of Praying Mantis from the Amazon Rainforest, Vespamantoida wherleyi gen. nov. sp. nov. (Mantodea, Mantoididae). PeerJ. 7:e7886. DOI: 10.7717/peerj.7886

Tuesday, October 8, 2019

[Entomology • 2019] Glaphyrosoma stephanosoltis • A New Species of King Cricket Glaphyrosoma Brunner von Wattenwyl, 1888 (Orthoptera: Anostostomatidae: Glaphyrosomatini) from Costa Rica with Behavioral Observations


Glaphyrosoma stephanosoltis
Richardson, Trimm, Paredes & Koehl, 2019


Abstract
A new king cricket species Glaphyrosoma stephanosoltis sp. nov. (Orthoptera: Anostostomatidae: Glaphyrosomatini) from mid-elevation tropical rainforests of Costa Rica is described. This new species represents the southernmost distribution of the genus Glaphyrosoma Brunner von Wattenwyl, 1888, which is widely distributed throughout Mexico, Guatemala, and Honduras. Biology of the new species is briefly described.

Keywords: Orthoptera, new species, feeding biology, Central America

The king cricket, Glaphyrosoma stephanosoltis, (Orthoptera: Anostostomatidae), captured in its natural habitat near the Solis Center in Costa Rica.
photo: Hojun Song

Family Anostostomatidae Saussure, 1859
Tribe Glaphyrosomatini Rentz & Weissman, 1973

Glaphyrosoma Brunner von Wattenwyl, 1888

Glaphyrosoma stephanosoltis Richardson, Trimm, Paderes, Koehl, & Song, sp. nov.

Etymology. From Latin “stephano” meaning crown and “soltis” referring to the Soltis Center for Research and Education, the type locality of the species. Therefore, stephanosoltis means “Crown of Soltis” referring to the first king cricket ever described at the facility. 

 Steven Richardson, Travis Trimm, Randell Paredes and Jonathan Koehl. 2019. A New Species of King Cricket Glaphyrosoma Brunner von Wattenwyl, 1888 (Orthoptera: Anostostomatidae: Glaphyrosomatini) from Costa Rica with Behavioral Observations. Zootaxa. 4671(1); 93–104. DOI: 10.11646/zootaxa.4671.1.7

New king cricket species discovery in Costa Rica phys.org/news/2019-10-king-cricket-species-discovery-costa.html via @physorg_com

[Entomology • 2019] Schistomitra joelmineti • First Record of the Genus Schistomitra Butler, 1881 (Lepidoptera, Epicopeiidae) from China, with the Description of A New Species


Schistomitra joelmineti Huang & Wang

in Huang, Zhang, Wang & Fan, 2019. 

Abstract
The epicopeiid moth genus Schistomitra Butler, 1881 is reported outside Japan for the first time, with a new species, Schistomitra joelmineti Huang & Wang, sp. nov., described from the southern part of Shaanxi and Gansu Province in China. Photographs of adults and genitalia are provided, and the distribution pattern of the genus is discussed.

Keywords: East Asia, Geometroidea, host plant, oriental swallowtail moth, Stewartia, taxonomy


Figures 1–8. Adults of Schistomitra spp. 1–3, 6–7 male 4, 5, 8 female
 1–5 Schistomitra joelmineti sp. nov. 6–8 Schistomitra funeralis. Scale bar: 1 cm.

Schistomitra joelmineti Huang & Wang, sp. nov.

Diagnosis: 
Schistomitra joelmineti sp. nov. is characterized and distinguished from S. funeralis (Figs 6–8, 15–17, 20) by the following characters:

1) the size is larger in both sexes, length of forewing 26–28 mm vs. 25–27 mm in males, 27–30 mm vs. 25 mm in females;
2) the forewing has the discoidal cell totally encircled by darkened veins, while the lower portion of discoidal cell remains pale yellow like its ground color in S. funeralis;
3) the blackish postmedian band on forewing upper side is narrower compared to the much wider band in S. funeralis;
4) the hind wing upper side has a much reduced blackish pattern in cell Rs and bases of cell 1A+2A and 3A, whereas the blackish pattern is better developed in all these cells in S. funeralis;

5) in the male genitalia the uncus is shorter with its tip nearly flat or slightly concave in the middle, while uncus is longer with its tip rounded in S. funeralis;
6) the sacculus is longer, and the apex of praesacculus forms a long, sharp, blade-like process pointing dorsally, while in S. funeralis the sacculus is shorter, with the apex only forming a short and rounded bulge;
7) the aedeagus is slightly thicker and longer, with the distal shaft more robust and the coecum larger, while the aedeagus is narrower and shorter, with distal shaft slenderer and coecum smaller in S. funeralis;
8) in the female genitalia, ductus bursae is more sclerotized, corpus bursae is smaller with a rounded signum, while in those of S. funeralis the ductus bursae is more membranous, the corpus bursae is larger, with the signum being elliptical.

Figures 21–23. Schistomitra joelmineti sp. nov. living adult and habitat
21 sucking on damp ground 22 resting on leaves 23 habitat of Schistomitra joelmineti sp. nov. in Chengguan Town, Ningshan County. 

Distribution: Currently this species is restricted to the southern part of Shaanxi Province and Gansu Province.

Etymology: The specific name joelmineti is named in honor of Prof. Joël Minet (Paris, France) who contributed greatly to the study of the family Epicopeiidae and kindly provided the first author with valuable literature when he began studying Epicopeiidae.

Biology: This species is univoltine, occurring from late April to early June. Adults are usually found sucking nutrients and water on damp ground (Fig. 21) or resting on leaves (Fig. 22) near the edge of the forest (Fig. 23) at altitude between 800 to 1800 m.


 Si-Yao Huang, Yuan Zhang, Min Wang and Xiao-Ling Fan. 2019. First Record of the Genus Schistomitra Butler, 1881 (Lepidoptera, Epicopeiidae) from China, with the Description of A New Species.  ZooKeys. 878: 145-155. DOI: 10.3897/zookeys.878.35364


Monday, October 7, 2019

[Entomology • 2019] Occidophasmata & Oriophasmata tax. nov. Old World and New World Phasmatodea: Phylogenomics Resolve the Evolutionary History of Stick and Leaf Insects


 Various members of Neophasmatodea:
(A–D): Occidophasmata - (A), couple of Pseudosermyle phalangiphora, Diapheromerinae (Mexico); (B), couple of Oreophoetes peruana, Diapheromerinae (Peru); (C), female of Metriophasma diocles, Pseudophasmatinae (Panama); (D), couple of Peruphasma schultei, Pseudophasmatinae (Peru);
(E–G): Oriophasmata - (E), female of Carausius morosus, Lonchodinae (India); (F), female of Heteropteryx dilatata, Heteropterygidae (Malaysia); (G), couple of Eurycantha calcarata, Lonchodinae (New Guinea)

in Simon, Letsch, Bank, et al., 2019. 
Photos by Christoph Seiler, Altlussheim, Germany.  

 Phasmatodea comprises over 3,000 extant species and stands out as one of the last remaining insect orders for which a robust, higher-level phylogenetic hypothesis is lacking. New research suggests that the extant diversity is the result of a surprisingly recent and rapid radiation that has been difficult to resolve with standard Sanger sequence data. In order to resolve the early branching events of stick and leaf insects, we analyzed transcriptomes from 61 species, including 38 Phasmatodea species comprising all major clades and 23 outgroup taxa, including all other Polyneoptera orders. Using a custom-made ortholog set based on reference genomes from four species, we identified on average 2,274 orthologous genes in the sequenced transcriptomes. We generated various sub-alignments and performed maximum-likelihood analyses on several representative datasets to evaluate the effect of missing data and matrix composition on our phylogenetic estimates. Based on our new data, we are able to reliably resolve the deeper nodes between the principal lineages of extant Phasmatodea. Among Euphasmatodea, we provide strong evidence for a basal dichotomy of Aschiphasmatodea and all remaining euphasmatodeans, the Neophasmatodea. Within the latter clade, we recovered a previously unrecognized major New World and Old World lineage, for which we introduce the new names Oriophasmata tax. nov. (“Eastern phasmids”) and Occidophasmata tax. nov. (“Western phasmids”). Occidophasmata comprise Diapheromerinae, Pseudophasmatinae, and Agathemera, whereas all remaining lineages form the Oriophasmata, including Heteropterygidae, Phylliinae, Bacillus, Lonchodidae (Necrosciinae + Lonchodinae), Clitumninae, Cladomorphinae, and Lanceocercata. We furthermore performed a divergence time analysis and reconstructed the historical biogeography for stick and leaf insects. Phasmatodea either originated in Southeast Asia or in the New World. Our results suggest that the extant distribution of Phasmatodea is largely the result of dispersal events in a recently and rapidly diversified insect lineage rather than the result of vicariant processes.

Keywords: phasmids, transcriptomes, historical biogeography, Polyneoptera, Euphasmatodea

FIGURE 1: Various members of Neophasmatodea: (A–D): Occidophasmata; (E–I): Oriophasmata.
(A), couple of Pseudosermyle phalangiphora, Diapheromerinae (Mexico); (B), couple of Oreophoetes peruana, Diapheromerinae (Peru); (C), female of Metriophasma diocles, Pseudophasmatinae (Panama); (D), couple of Peruphasma schultei, Pseudophasmatinae (Peru); (E), female of Carausius morosus, Lonchodinae (India); (F), female of Heteropteryx dilatata, Heteropterygidae (Malaysia); (G), couple of Eurycantha calcarata, Lonchodinae (New Guinea); (H), female of Extatosoma tiaratum, Lanceocercata (Australia); (I), couple of Diapherodes gigantea, Cladomorphinae (Grenada). Photos by Christoph Seiler, Altlussheim, Germany.



FIGURE 2: Time-calibrated phylogeny of Phasmatodea. Inferred phylogenetic relationships based on dataset AAdecisive (387,987 aa positions, 205 metapartitions). Colored circles represent bootstrap support derived from 100 BS. Node dates (posterior mean) were inferred using the dataset AAdecisive reduced to sites containing >95% data completeness, and five fossil calibrations. Error bars represent 95% confidence intervals. Fossils used for calibrations are indicated as numbers in black circles at nodes: 1: Nel and Delfosse (2011), 2: Wedmann et al. (2007), 3: Sellick (1994), 4, 5: Poinar (2011) (see also Table 1). OCCIDOPH., Occidophasmata; Neo., Neogene; Q., Quaternary.

FIGURE 4: Ancestral range estimates of Phasmatodea for the BioGeoBEARS DIVALIKE+J model. The nodal pie charts show the relative probability of the geographic ranges according to the in-figure color code. OCCIDOPH., Occidophasmata, Jura., Jurassic, Neo., Neogene, Q., Quaternary.

Conclusion and Outlook
Our study confirms the power of phylogenomic approaches for inferring evolutionary relationships that have been difficult to assess in the past by yielding a well-supported topology at the base of the tree of life of stick and leaf insects. We provide strong evidence for resolving the deep phylogenetic nodes among all major lineages of Phasmatodea, and were furthermore able to date the individual divergence events and reconstruct their biogeographic history. Our study provides a substantial basis for establishing a natural classification of the stick and leaf insects and for further developing the role of phasmatodeans as emerging model systems in evolutionary research. Future studies need to address minor but crucial taxonomic problems that still await revelation such as the phylogenetic placement of the Southeast Asian Stephanacridini, the African Gratidiini, Bacillinae, and Palophinae, and the Neotropical Heteronemiini, by for instance, applying DNA enrichment methods in order to generate phylogenetically informative data sets that can be combined with those generated in the present study.


Sabrina Simon, Harald Letsch, Sarah Bank, Thomas R. Buckley, Alexander Donath, Shanlin Liu, Ryuichiro Machida, Karen Meusemann, Bernhard Misof, Lars Podsiadlowski, Xin Zhou, Benjamin Wipfler and Sven Bradler. 2019. Old World and New World Phasmatodea: Phylogenomics Resolve the Evolutionary History of Stick and Leaf Insects.  Front. Ecol. Evol. DOI: 10.3389/fevo.2019.00345  

Sunday, October 6, 2019

[Entomology • 2019] Katydids (Orthoptera: Tettigoniidae) of Gorongosa National Park and Central Mozambique


Gorongosa carri 
Naskrecki & Guta, 2019


Abstract
A list of 60 species of the Tettigoniidae (Orthoptera) recorded from Gorongosa National Park and provinces Sofala and Manica in central Mozambique is provided and their natural history is discussed. Of these, 58 species are illustrated and bioacoustic data are presented for 47 species. Two new genera and 9 new species are described: Gorongosa carri gen. et sp. n., Ovonotus abreuae gen. et sp. n., Afroagraecia muagurai sp. n., Enyaliopsis iaculator sp. n., Eurycorypha parkeri sp. n., Eurycorypha stalmansi sp. n., Eulioptera carolli sp. n., Eulioptera mutembai sp. n., and Parpyrrhicia guytonae sp. n. Four species of Ruspolia are recognized as potentially new and their bioacoustic data are presented. Pseudorhynchus pungens meridionalis Ragge, 1969 is synonymized with Pseudorhynchus pungens pungens (Schaum, 1853); Angustithorax spiniger Massa, 2015 is synonymized with Oxyecous magnus Ragge, 1956; and the synonymy of Lanista africana (Walker, 1870) with Lanista annulicornis (Walker, 1869) is reversed. Two species, G. carri and O. abreuae, appear to be endemic to Mt. Gorongosa and 24 species are recorded for the first time from Mozambique.

Keywords: Orthoptera, katydids, new species, new genera, endemism, species list, bioacoustics, Mozambique




Piotr Naskrecki and Ricardo Guta. 2019. Katydids (Orthoptera: Tettigoniidae) of Gorongosa National Park and Central Mozambique. Zootaxa. 4682(1); 1-119. DOI: 10.11646/zootaxa.4682.1.1  

Thursday, October 3, 2019

[Entomology • 2019] Hermatobates lingyangjiaoensis • First Record of Hermatobatidae (Hemiptera: Heteroptera) from China


Hermatobates lingyangjiaoensis 
 Luo, Chen, Wang & Xie, 2019


Abstract
The family Hermatobatidae Poisson, 1965 is recorded for the first time from China and Hermatobates lingyangjiaoensis sp. n. is described. Photographs of the male and female habitus, legs, metasternum, and male genitalic structures, and scanning electron micrographs of the male metasternum and propleuron are provided. A key to all the species currently recognized in the H. weddi species group is presented. Distribution maps for the species of Hermatobates in China and Southeast Asia are also provided. Further, a photograph documenting the feeding of Hermatobates on Halovelia is presented for the first time to serve as direct evidence of the feeding habits of Hermatobates.

Keywords: Hemiptera, China, Heteroptera, Hermatobatidae, Hermatobates, new species




  Hermatobates lingyangjiaoensis sp. n. 


Jiuyang Luo, Pingping Chen, Yanhui Wang and Qiang Xie. 2019. First Record of Hermatobatidae from China, with Description of Hermatobates lingyangjiaoensis sp. n. (Hemiptera: Heteroptera). 4679(3); 527–538. DOI: 10.11646/zootaxa.4679.3.7



Tuesday, October 1, 2019

[Entomology • 2019] Systematics and Biogeography of the Genus Scaria Bolívar, 1887 (Orthoptera: Tetrigidae: Batrachideinae)


Batrachidea brevis (Hancock, 1909)

in Cadena-Castañeda, Mello Mendes, Silva, Granda, García & Tumbrinck. 2019.  

Abstract
The Amazon rainforest is the world’s most extensive tropical rainforest, holding a considerable ecological and taxonomic diversity. Speciation in this region arises from multiple factors, such as topography, climate fluctuations, oceanic transgression, vegetation and the delimitation of zones circumscribed by sub-basins within the greater Amazon basin. Different scenarios have been proposed to better understand the diversification of Amazonian taxa, whether by Pleistocene refugia or by areas of endemism.

The genus Scaria is distributed mostly in Amazonia, with a single species that ranges from the Tumbes-Chocó-Magdalena ecoregion well into Central America all the way to southern Nicaragua. Eight species are currently recognized, with three additional described here as new: Scaria rafaeli sp. nov., S. jonasi sp. nov. and S. granti sp. nov., and the status of S. laeta stat. resurr. is revalidated. Two new combinations are established: S. verutum comb. nov. (formerly placed in Rehnidium Grant, 1956) and Batrachidea brevis comb. nov. (formerly placed in Scaria). New synonym is proposed: Batrachidea brevis (Hancock, 1909) = Batrachidea inermis Hebard, 1923 syn. nov. Lectotypes and paralectotypes were selected for S. laeta, S. maculata and S. lineata, as well as the neotypes for S. hamata and S. boliviana. An updated key to species of Scaria is also provided.

A cladistic analysis for 15 species was performed (12 in the inner group and 3 in the outer group) with 40 morphological characters, confirming the monophyly of Scaria. A biogeographical analysis of dispersion-vicariance indicates that the origin of the genus was probably in the Inambari endemism center as the only reconstruction of the resulting ancestral distribution, five dispersions and three vicariance events being postulated. These suggest that both types of events are equally important in the current configuration of the distribution in Scaria. Vicariance events arise mostly by isolation of the species because of the uplift of the Andes and the dispersion events comprise four waves originating from the ancestral range into central and east Amazonia.

Keywords: Orthoptera, Amazon, Andes, Biogeographic Chocó, Neotropics, vicariance, dispersión, Batrachidea, Rehnidium, taxonomy, new taxa, new synonym



Batrachidea brevis (Hancock, 1909)


Oscar J. Cadena-Castañeda, Diego Matheus De Mello Mendes, Daniela Santos Martins Silva, Juan Manuel Cardona Granda, Alexander García García and Josef Tumbrinck. 2019. Systematics and Biogeography of the Genus Scaria Bolívar, 1887 (Orthoptera: Tetrigidae: Batrachideinae). Zootaxa. 4675(1); 1-65. DOI: 10.11646/zootaxa.4675.1.1

Monday, September 30, 2019

[Entomology • 2019] A Taxonomic Monograph of the Genus Solariola Flach, 1908 (Coleoptera: Curculionidae: Entiminae)


 Solariola doderoi A. & F. Solari (1923)

in Bellò, Osella & Baviera, 2019. 

Abstract
A revision of the genus Solariola Flach, 1908 of the tribe Peritelini Lacordaire (1863) (Curculionidae: Entiminae) which includes forty-three species is completed. According to morphological characters and distribution, the species are divided into three informal groups (the number of species ascribed to the group is in brackets). These are the Solariola doderoi group (15), the Solariola gestroi group (14) and the Solariola paganettii group (14). We present keys for the identification of the genus among the Palaeartic Peritelini and keys to identify all species groups and species. Distribution maps and data on ecology and phenology are also provided. In addition to the following nine species already belonging to the genus we list 34 new species as well: Solariola gestroi (A. & F. Solari, 1903), Solariola paganettii (Flach, 1905), Solariola doderoi A. & F. Solari (1923), Solariola hirtula (A. & F. Solari,1923), Solariola vitalei A. & F. Solari (1923), Solariola ruffoi Osella & Di Marco (1996), Solariola angelae Baviera (2015), Solariola fraterna Baviera (2015), Solariola pesarinii Baviera (2015); Solariola angelinii Bellò, Osella & Baviera sp.n., Solariola benellii Bellò, Osella & Baviera sp.n., Solariola bucolorum Bellò, Osella & Baviera sp.n., Solariola cajetanibelloi Bellò, Osella & Baviera sp.n., Solariola calida Bellò, Osella & Baviera sp.n., Solariola comata Bellò, Osella & Baviera sp.n., Solariola diottii Bellò, Osella & Baviera sp.n., Solariola fancelloi Bellò, Osella & Baviera sp.n., Solariola forbixi Bellò, Osella & Baviera sp.n., Solariola gratiensis Bellò, Osella & Baviera sp.n., Solariola hyblensis Bellò, Osella & Baviera sp.n., Solariola ientilei Bellò, Osella & Baviera sp.n., Solariola margaritae Bellò, Osella & Baviera sp.n., Solariola mariaeclarae Bellò, Osella & Baviera sp.n., Solariola mariaesilvanae Bellò, Osella & Baviera sp.n., Solariola mariaetheresiae Bellò, Osella & Baviera sp.n., Solariola melonii Bellò, Osella & Baviera sp.n., Solariola nemoralis Bellò, Osella & Baviera sp.n., Solariola normanna Bellò, Osella & Baviera sp.n., Solariola obsoleta Bellò, Osella & Baviera sp.n., Solariola pacei Bellò, Osella & Baviera sp.n., Solariola paulimagrinii Bellò, Osella & Baviera sp.n., Solariola pentaphyllica Bellò, Osella & Baviera sp.n., Solariola petriolii Bellò, Osella & Baviera sp.n., Solariola poggii Bellò, Osella & Baviera sp.n., Solariola raphaelis Bellò, Osella & Baviera sp.n., Solariola rosae Bellò, Osella & Baviera sp.n., Solariola sabellai Bellò, Osella & Baviera sp.n., Solariola saccoi Bellò, Osella & Baviera sp.n., Solariola sbordonii Bellò, Osella & Baviera sp.n., Solariola selinusia Bellò, Osella & Baviera sp.n., Solariola tedeschii Bellò, Osella & Baviera sp.n., Solariola venusta Bellò, Osella & Baviera sp.n., Solariola zoiai Bellò, Osella & Baviera sp.n..

Keywords: Coleoptera, Biodiversity, Southern Italy, weevils, taxonomy, new species, zoogeography




Cesare Bellò, Giuseppe Osella and Cosimo Baviera. 2019. A Taxonomic Monograph of the Genus Solariola Flach, 1908 (Coleoptera: Curculionidae: Entiminae). Zootaxa.  4676(1);1-261. DOI: 10.11646/zootaxa.4676.1.1

Wednesday, September 25, 2019

[Entomology • 2019] Ischnomera sicula • A New Ischnomera of the I. xanthoderes (Mulsant, 1858) complex (Coleoptera: Oedemeridae) from Sicily


Ischnomera sicula 
Bologna, Poloni & Vázquez, 2019


Abstract
A new Ischnomera from northern Sicily is described. Besides this species, in the western Mediterranean I. xanthoderes complex were distinct one species from the Iberian peninsula and southern France (I. xanthoderes), and one from northwestern Africa (I. tenietensis). All species are figured and a key to the species is published.

Keywords: Coleoptera, Italy, new species, taxonomy, Tenebrionoidea, western Mediterranean

 Ischnomera sicula n.sp. in the field (Sicily, Palermo prov., Madonie, Piano Battaglietta,
photo C. Muscarella). 

Ischnomera sicula n.sp. 

Ethymology. The name of the species refers to its distribution, limited to the mountains of northern Sicily.


Marco A. Bologna, Riccardo Poloni and Xavier A. Vázquez. 2019. A New Ischnomera of the I. xanthoderes (Mulsant, 1858) complex (Coleoptera: Oedemeridae) from Sicily. Zootaxa. 4671(4); 541–550. DOI: 10.11646/zootaxa.4671.4.5


[Entomology • 2019] Rhamphomyia Meigen (Diptera: Empididae) of the Canadian Arctic Archipelago, Greenland and Iceland


Rhamphomyia (Pararhamphomyia) septentrionalis 

Sinclair, Vajda, Saigusa, Shamshev & Wheeler, 2019


Abstract
Rhamphomyia of the Canadian Arctic Archipelago, Greenland and Iceland, comprising 23 species, including five new species, are revised: R. (Ctenempis) albopilosa Coquillett, R. (Dasyrhamphomyia) erinacioides Malloch, R. (Dasyrhamphomyia) hovgaardii Holmgren, R. (Dasyrhamphomyia) leptidiformis Frey, R. (Dasyrhamphomyia) nigrita Zetterstedt, R. (Eorhamphomyia) shewelli Sinclair, Vajda, Saigusa & Shamshev sp. nov., R. (Pararhamphomyia) diversipennis Becker, R. (Pararhamphomyia) filicauda Henriksen & Lundbeck, R. (Pararhamphomyia) frigida Sinclair, Vajda, Saigusa & Shamshev sp. nov., R. (Pararhamphomyia) helleni Frey, R. (Pararhamphomyia) hilariformis Frey, R. (Pararhamphomyia) hoeli Frey, R. (Pararhamphomyia) kjellmanii Holmgren, R. (Pararhamphomyia) lymaniana Sinclair, Vajda, Saigusa & Shamshev sp. nov., R. (Pararhamphomyia) omissinervis Becker, R. (Pararhamphomyia) petervajdai Sinclair, Vajda, Saigusa & Shamshev sp. nov.R. (Pararhamphomyiaseptentrionalis Sinclair, Vajda, Saigusa & Shamshev sp. nov., R. (Pararhamphomyia) simplex Zetterstedt, R. (Pararhamphomyia) ursinella Melander, R. herschelli Malloch, R. hirtula Zetterstedt, R. laevigata Loew, R. setosa Coquillett. The following six new synonyms are proposed: R. calvimontis Cockerell, 1916 and R. wuorentausi Frey, 1922 = R. albopilosa Coquillett, 1900; R. fridolini Frey, 1950 = R. laevigata Loew, 1861; R. hirticula Collin, 1937 = R. setosa Coquillett, 1895; R. uralensis Becker, 1915 = R. kjellmanii Holmgren, 1880; R. zaitzevi Becker, 1915 = R. hovgaardii Holmgren, 1880. Lectotypes are designated for the following species: R. diversipennis Becker, R. filicauda Henriksen & Lundbeck, R. helleni Frey, R. herschelli Malloch, R. hirticula Collin, R. hoeli Frey, R. leptidiformis Frey, R. omissinervis Becker, R. setosa Coquillett, R. uralensis Becker, R. wuorentausi Frey, R. zaitzevi Becker. A neotype is designated for R. laevigata Loew. Keys to male and female species of Rhamphomyia and distribution maps of this region are provided. DNA barcode data are presented for 16 species of arctic Rhamphomyia.

Keywords: Diptera, Empididae, Rhamphomyia, new species, arctic, Nearctic

Rhamphomyia (Pararhamphomyiaseptentrionalis 


Bradley J. Sinclair, Élodie A. Vajda, Toyohei Saigusa,  Igor V. Shamshev and Terry A. Wheeler. 2019. Rhamphomyia Meigen of the Canadian Arctic Archipelago, Greenland and Iceland (Diptera: Empididae). Zootaxa. 4670(1); 1-94. DOI: 10.11646/zootaxa.4670.1.1