Changes in Lp-PLA 2 are associated with elevated alanine aminotransferase levels: A nested case-control study in a three-year prospective cohort

Background/Aim: Elevation in liver enzymes and hepatic fat may indicate a higher susceptibility to cardiovascular disease (CVD). This research sought to find anthropometric/biochemical variables significantly related to the alanine aminotransferase (ALT) increase in healthy populations. Methods: Nine hundred healthy subjects were included in a 3-year prospective cohort study. The initial screening revealed that 538 were found to be nondiabetic (fasting glucose < 126 mg/dL) and had normal ALT levels. Among them, 79 individuals with slightly elevated ALT levels after three years were assigned to the elevated ALT group. Of the remaining 459 participants, 241 subjects matched to the increased ALT group were the control group. Results: After three years of follow-up, individuals with elevated ALT showed notably higher aspartate aminotransferase (AST), ALT, gamma-glutamyl-transferase (g-GT), high sensitivity C-reactive protein (hs-CRP), lipoprotein-associated phospholipase A2 (Lp-PLA2 ) activity, oxidised low-density lipoprotein (ox-LDL), urinary 8-epi-prostaglandin F2a (8-epi-PGF2a) levels and brachial-ankle pulse wave velocity (ba-PWV) in comparison to the control group. Changes (D) in ALT showed a positive correlation with D AST, D gammaGT, D hs-CRP, D Lp-PLA2 activity, D ox-LDL, D urinary 8-epi-PGF2a and D ba-PWV. Furthermore, a direct positive link was observed between the D Lp-PLA2 activity and D AST, D ox-LDL and D ba-PWV. Conclusion: Increased Lp-PLA2 activity and other CVD risk indicators were observed to have a pronounced association with elevated ALT levels. This mild ALT elevation could potentially contribute to chronic low-grade inflammation

Prenatal allergen and diesel exhaust exposure and their effects on allergy in adult offspring mice

Multiple studies have suggested that prenatal exposure to either allergens or air pollution may increase the risk for the development of allergic immune responses in young offspring. However, the effects of prenatal environmental exposures on adult offspring have not been well-studied. We hypothesized that combined prenatal exposure to Aspergillus fumigatus (A. fumigatus) allergen and diesel exhaust particles will be associated with altered IgE production, airway inflammation, airway hyperreactivity (AHR), and airway remodeling of adult offspring. Following sensitization via the airway route to A. fumigatus and mating, pregnant BALB/c mice were exposed to additional A. fumigatus and/or diesel exhaust particles. At age 9-10 weeks, their offspring were sensitized and challenged with A. fumigatus. We found that adult offspring from mice that were exposed to A. fumigatus or diesel exhaust particles during pregnancy experienced decreases in IgE production. Adult offspring of mice that were exposed to both A. fumigatus and diesel exhaust particles during pregnancy experienced decreases in airway eosinophilia. These results suggest that, in this model, allergen and/or diesel administration during pregnancy may be associated with protection from developing systemic and airway allergic immune responses in the adult offspring

Structural and physicochemical effects on the starch quality of the high-quality wheat genotype caused by delayed sowing

BackgroundBread wheat is one of the most important food crops associated with ensuring food security and human nutritional health. The starch quality is an important index of high-quality wheat. It is affected by a complex series of factors; among which, suitable sowing time is a key factor.Aim and methodsTo analyze the integrative effects of sowing time on the starch quality of high-quality wheat, in the present study, we selected a high-quality bread wheat cultivar Jinan 17 and investigated the effect of different sowing times on the starch properties and the related genes by analyzing X-ray diffraction patterns, apparent amylose content, thermal properties, pasting properties, in vitro starch digestibility, and qRT-PCR. Meanwhile, we also investigated the agronomic and yield performance that may be associated with the starch properties.ResultsDelayed sowing had little effect on starch crystalline morphology, but there was a tendency to reduce the formation of crystals within wheat starch granules: (1) delayed sowing for 15 days altered the thermal properties of starch, including onset, peak and termination temperatures, and enthalpy changes; (2) delayed sowing for 30 days changed the thermal characteristics of starch relatively insignificant; (3) significant differences in pasting characteristics occurred: peak viscosity and hold-through viscosity increased, while final viscosity, breakdown viscosity, and setback viscosity tended to increase and then decrease, suggesting that delayed sowing caused changes in the surface of the starch granules resulting in a decrease in digestibility. Analysis of related genes showed that several key enzymes in starch biosynthesis were significantly affected by delayed sowing, leading to a reduction in apparent straight-chain starch content. In addition to starch properties, thousand-kernel weight also increased under delayed sowing conditions compared with normal sowing.ConclusionThe impact of delayed sowing on starch quality is multifaceted and complex, from the fine structure, and functional properties of the starch to the regulation of key gene expression. Our study holds significant practical value for optimizing wheat planting management and maximizing the potential in both quality and yield

Thecobathra paranas Fan, Jin & Li, 2008, sp. nov.

&lt;i&gt;Thecobathra paranas&lt;/i&gt; sp. nov. &lt;p&gt;(Figs. 6, 13)&lt;/p&gt; &lt;p&gt; &lt;b&gt;Type material.&lt;/b&gt; Holotype: ɗ, &lt;b&gt;CHINA:&lt;/b&gt; Ruili [24&deg;00'N, 97&deg;50'E], Yunnan Province, 1000 m, 7.viii.2005, coll. Yingdang Ren, genitalia slide no. FXM07040.&lt;/p&gt; &lt;p&gt; &lt;b&gt;Diagnosis.&lt;/b&gt; This species is similar to &lt;i&gt;T. anas&lt;/i&gt; (Stringer) in the male genitalia, but can be distinguished from it by the ventral plate of gnathos, in which the anterior margin is spined and concave inward medially, and by the valva, in which the ventral margin roundly protrudes between the apex of the sacculus and the tooth.&lt;/p&gt; &lt;p&gt; &lt;b&gt;Description.&lt;/b&gt; Adult (Fig. 6): Wing expanse 13.0 mm. Head white, with long rough scales on vertex. Antenna white. Labial palpus white, pale yellow on ventral surface of second segment, upturned. Thorax and tegula snow white. Forewing white, tinged with greyish brown; costal margin with basal 1/7 black; cilia white. Hindwing pale brown; cilia white. Legs white except tarsi somewhat pale yellowish and hind tibia with a black dot at apex of either side.&lt;/p&gt; &lt;p&gt;Male genitalia (Fig. 13): Socius somewhat footlike in shape, slightly narrowed at base; dorsal edge expanded outward at 1/3, forming a blunt angle, then straight to near apex, apex pointed and curved down; ventral edge gently arched. Tuba analis membranous. Ventral plate of gnathos more or less trumpet shaped, anterior margin spined, concave inward medially. Valva broad, uprising; basal 1/4 uniformly narrowed, widened at 1/4, then gradually narrowed to rounded apex; costa curved medially; ventral margin gently arched, with a tooth near middle, roundly protruding between apex of sacculus and the tooth. Sacculus narrow, concave inward. Saccus with posterior half widely V-shaped, anterior half long triangular, rounded at apex. Phallus about 1.5 times length of saccus, slender and slightly curved; with two rows of dentation: one row from 2/ 5 to apex, the other from distal 1/3 to apex.&lt;/p&gt; &lt;p&gt;Female: Unknown.&lt;/p&gt; &lt;p&gt; &lt;b&gt;Distribution.&lt;/b&gt; China (Yunnan).&lt;/p&gt; &lt;p&gt; &lt;b&gt;Etymology.&lt;/b&gt; The specific name is derived from the Greek &lt;i&gt;par&lt;/i&gt; - and &lt;i&gt;anas&lt;/i&gt;, the name of another species, referring to their similarity.&lt;/p&gt;Published as part of &lt;i&gt;Fan, Ximei, Jin, Qing &amp; Li, Houhun, 2008, Seven new species and a checklist of the genus Thecobathra Meyrick from China (Lepidoptera: Yponomeutidae), pp. 13-24 in Zootaxa 1821&lt;/i&gt; on page 20, DOI: &lt;a href="http://zenodo.org/record/183025"&gt;10.5281/zenodo.183025&lt;/a&gt

Nonlinear Vibration Control Experimental System Design of a Flexible Arm Using Interactive Actuations from Shape Memory Alloy

The flexible arm easily vibrates due to its thin structural characteristics, which affect the operation accuracy, so reducing the vibration of the flexible arm is a significant issue. Smart materials are very widely used in the research topic of vibration suppression. Considering the hysteresis characteristic of the smart materials, based on previous simulation research, this paper proposes an experimental system design of nonlinear vibration control by using the interactive actuation from shape memory alloy (SMA) for a flexible arm. The experiment system was an interactive actuator&ndash;sensor&ndash;controller combination. The vibration suppression strategy was integrated with an operator-based vibration controller, a designed integral compensator and the designed n-times feedback loop. In detail, a nonlinear vibration controller based on operator theory was designed to guarantee the robust stability of the flexible arm. An integral compensator based on an estimation mechanism was designed to optimally reduce the displacement of the flexible arm. Obtaining the desired tracking performance of the flexible arm was a further step, by increasing the n-times feedback loop. From the three experimental cases, when the vibration controller was integrated with the designed integral compensator, the vibration displacement of the flexible arm was much reduced compared to that without the integral compensator. Increasing the number of n-times feedback loops improves the tracking performance. The desired vibration control performance can be satisfied when n tends to infinity. The conventional PD controller stabilizes the vibration displacement after the 7th vibration waveform, while the vibration displacement approaches zero after the 4th vibration waveform using the proposed vibration control method, which is proved to be faster and more effective in controlling the flexible arm&rsquo;s vibration. The experimental cases verify the effectiveness of the proposed interactive actuation vibration control approach. It is observed from the experimental results that the vibration displacement of the flexible arm becomes almost zero within less time and with lower input power, compared with a traditional controller

Nonlinear Fault-Tolerant Vibration Control for Partial Actuator Fault of a Flexible Arm

This paper presents a nonlinear fault-tolerant vibration control system for a flexible arm, considering partial actuator fault. A lightweight flexible arm with lower stiffness will inevitably cause vibration which will impair the performance of the high-precision control system. Therefore, an operator-based robust nonlinear vibration control system is integrated by a double-sided interactive controller actuated by the Shape Memory Alloy (SMA) actuators for the flexible arm. Furthermore, to improve the safety and reliability of the safety-critical application, fault-tolerant dynamics for partial actuator fault are considered as an essential part of the proposed control system. The experimental cases are set to the partial actuator as faulty conditions, and the proposed vibration control scheme has fault-tolerant dynamics which can still effectively stabilize the vibration displacement. The reconfigurable controller improves the fault-tolerant performance by shortening the vibration time and reducing the vibration displacement of the flexible arm. In addition, compared with a PD controller, the proposed nonlinear vibration control has better performance than the traditional controller. The experimental results show that the effectiveness of the proposed method is confirmed. That is, the safety and reliability of the proposed fault-tolerant vibration control are verified even if in the presence of an actuator fault

Thecobathra

Checklist of &lt;i&gt;Thecobathra&lt;/i&gt; of China &lt;p&gt; &lt;i&gt;Thecobathra acrivalvata&lt;/i&gt; &lt;b&gt;sp. nov.&lt;/b&gt;&lt;/p&gt; &lt;p&gt;Distribution: China (Guizhou).&lt;/p&gt; &lt;p&gt; &lt;i&gt;Thecobathra albana&lt;/i&gt; Liu, 1980&lt;/p&gt; &lt;p&gt; &lt;i&gt;Thecobathra albana&lt;/i&gt; Liu, 1980: 36.&lt;/p&gt; &lt;p&gt;Distribution: China (Hainan, Jiangxi).&lt;/p&gt; &lt;p&gt; &lt;i&gt;Thecobathra anas&lt;/i&gt; (Stringer, 1930)&lt;/p&gt; &lt;p&gt; &lt;i&gt;Niphonympha anas&lt;/i&gt; Stringer, 1930: 420. &lt;i&gt;Scythropiodes unimaculata&lt;/i&gt; Matsumura, 1931: 1099. &lt;i&gt;Pseudocalantica anas&lt;/i&gt; (Stringer); Friese, 1960: 37. &lt;i&gt;Thecobathra anas&lt;/i&gt; (Stringer); Moriuti, 1971: 232. Distribution: China (Anhui, Guizhou, Hubei, Hunan, Jiangxi, Sichuan, Yunnan, Zhejiang), Japan.&lt;/p&gt; &lt;p&gt; &lt;i&gt;Thecobathra argophenes&lt;/i&gt; (Meyrick, 1907)&lt;/p&gt; &lt;p&gt; &lt;i&gt;Pyrozela&lt;/i&gt; &lt;i&gt;argophenes&lt;/i&gt; Meyrick, 1907: 747. &lt;i&gt;Niphonympha argophenes&lt;/i&gt;; Meyrick, 1914: 45. &lt;i&gt;Thecobathra argophenes&lt;/i&gt; (Meyrick); Moriuti, 1971: 245. Distribution: China (Yunnan, Zhejiang), India.&lt;/p&gt; &lt;p&gt; &lt;i&gt;Thecobathra badagongshana&lt;/i&gt; &lt;b&gt;sp. nov.&lt;/b&gt;&lt;/p&gt; &lt;p&gt;Distribution: China (Hunan).&lt;/p&gt; &lt;p&gt; &lt;i&gt;Thecobathra basilobata&lt;/i&gt; &lt;b&gt;sp. nov.&lt;/b&gt;&lt;/p&gt; &lt;p&gt;Distribution: China (Taiwan).&lt;/p&gt; &lt;p&gt; &lt;i&gt;Thecobathra bidentata&lt;/i&gt; Liu, 1980&lt;/p&gt; &lt;p&gt; &lt;i&gt;Thecobathra bidentata&lt;/i&gt; Liu, 1980: 38.&lt;/p&gt; &lt;p&gt;Distribution: China (Jiangxi).&lt;/p&gt; &lt;p&gt; &lt;i&gt;Thecobathra chiona&lt;/i&gt; Liu, 1983&lt;/p&gt; &lt;p&gt; &lt;i&gt;Thecobathra chiona&lt;/i&gt; Liu, 1983: 81.&lt;/p&gt; &lt;p&gt;Distribution: China (Sichuan).&lt;/p&gt; &lt;p&gt; &lt;i&gt;Thecobathra delias&lt;/i&gt; (Meyrick, 1913)&lt;/p&gt; &lt;p&gt; &lt;i&gt;Calantica delias&lt;/i&gt; Meyrick, 1913: 148.&lt;/p&gt; &lt;p&gt; &lt;i&gt;Niphonympha delias&lt;/i&gt;; Meyrick, 1914: 45.&lt;/p&gt; &lt;p&gt; &lt;i&gt;Thecobathra delias&lt;/i&gt;; Moriuti, 1971: 242. Distribution: China (Guangdong, Hunan, Jiangsu, Sichuan, Xizang, Yunnan, Zhejiang), India.&lt;/p&gt; &lt;p&gt; &lt;i&gt;Thecobathra eta&lt;/i&gt; (Moriuti, 1963)&lt;/p&gt; &lt;p&gt; &lt;i&gt;Pseudocalantica eta&lt;/i&gt; Moriuti, 1963: 218. &lt;i&gt;Thecobathra eta&lt;/i&gt; (Moriuti); Moriuti, 1971: 238. Distribution: China (Zhejiang), Japan.&lt;/p&gt; &lt;p&gt; &lt;i&gt;Thecobathra flavida&lt;/i&gt; Yu and Li, 2001&lt;/p&gt; &lt;p&gt; &lt;i&gt;Thecobathra flavida&lt;/i&gt; Yu and Li, 2001: 118. Distribution: China (Hubei).&lt;/p&gt; &lt;p&gt; &lt;i&gt;Thecobathra kappa&lt;/i&gt; (Moriuti, 1963)&lt;/p&gt; &lt;p&gt; &lt;i&gt;Pseudocalantica kappa&lt;/i&gt; Moriuti, 1963: 220. &lt;i&gt;Thecobathra kappa&lt;/i&gt; (Moriuti); Moriuti, 1971: 240. Distribution: China (Sichuan, Taiwan).&lt;/p&gt; &lt;p&gt; &lt;i&gt;Thecobathra lambda&lt;/i&gt; (Moriuti, 1963)&lt;/p&gt; &lt;p&gt; &lt;i&gt;Pseudocalantica lambda&lt;/i&gt; Moriuti, 1963: 222. &lt;i&gt;Thecobathra lambda&lt;/i&gt; (Moriuti); Moriuti, 1971: 237. Distribution: China (Hunan, Jiangxi, Sichuan, Taiwan, Zhejiang), Thailand.&lt;/p&gt; &lt;p&gt; &lt;i&gt;Thecobathra latibasis&lt;/i&gt; &lt;b&gt;sp. nov.&lt;/b&gt;&lt;/p&gt; &lt;p&gt;Distribution: China (Guangxi).&lt;/p&gt; &lt;p&gt; &lt;i&gt;Thecobathra longisaccata&lt;/i&gt; &lt;b&gt;sp. nov.&lt;/b&gt;&lt;/p&gt; &lt;p&gt;Distribution: China (Yunnan).&lt;/p&gt; &lt;p&gt; &lt;i&gt;Thecobathra microsignata&lt;/i&gt; Liu, 1980&lt;/p&gt; &lt;p&gt; &lt;i&gt;Thecobathra microsignata&lt;/i&gt; Liu, 1980: 37. Distribution: China (Yunnan).&lt;/p&gt; &lt;p&gt; &lt;i&gt;Thecobathra ovata&lt;/i&gt; Liu, 1980&lt;/p&gt; &lt;p&gt; &lt;i&gt;Thecobathra ovata&lt;/i&gt; Liu, 1980: 37.&lt;/p&gt; &lt;p&gt;Distribution: China (Jiangxi).&lt;/p&gt; &lt;p&gt; &lt;i&gt;Thecobathra paranas&lt;/i&gt; &lt;b&gt;sp. nov.&lt;/b&gt;&lt;/p&gt; &lt;p&gt;Distribution: China (Yunnan).&lt;/p&gt; &lt;p&gt; &lt;i&gt;Thecobathra partinuda&lt;/i&gt; &lt;b&gt;sp. nov.&lt;/b&gt;&lt;/p&gt; &lt;p&gt;Distribution: China (Taiwan).&lt;/p&gt; &lt;p&gt; &lt;i&gt;Thecobathra sororiata&lt;/i&gt; Moriuti, 1971&lt;/p&gt; &lt;p&gt; &lt;i&gt;Thecobathra sororiata&lt;/i&gt; Moriuti, 1971: 240. &lt;i&gt;Niphonympha delias&lt;/i&gt; Meyrick; Meyrick, 1935: 92 (not Meyrick, 1913). &lt;i&gt;Pseudocalantica delias&lt;/i&gt; (Meyrick); Friese, 1962: 305 (not Meyrick, 1913). &lt;i&gt;Thecobathra nivalis&lt;/i&gt; Moriuti, 1971: 241; Liu, 1980: 33. Distribution: China (Anhui, Henan, Hunan, Jiangsu, Jiangxi, Sichuan, Zhejiang).&lt;/p&gt; &lt;p&gt; &lt;i&gt;Thecobathra tetragona&lt;/i&gt; Liu, 1983&lt;/p&gt; &lt;p&gt; &lt;i&gt;Thecobathra tetragona&lt;/i&gt; Liu, 1983: 80.&lt;/p&gt; &lt;p&gt;Distribution: China (Sichuan).&lt;/p&gt; &lt;p&gt; &lt;i&gt;Thecobathra yasudai&lt;/i&gt; (Moriuti, 1965)&lt;/p&gt; &lt;p&gt; &lt;i&gt;Pseudocalantica yasudai&lt;/i&gt; Moriuti, 1965: 7. &lt;i&gt;Thecobathra yasudai&lt;/i&gt;; Moriuti, 1971: 235. Distribution: China (Yunnan), Nepal, Sikkim.&lt;/p&gt; &lt;p&gt; &lt;i&gt;Thecobathra yunnana&lt;/i&gt; Liu, 1984&lt;/p&gt; &lt;p&gt; &lt;i&gt;Thecobathra yunnana&lt;/i&gt; Liu, 1984: 324.&lt;/p&gt; &lt;p&gt;Distribution: China (Yunnan).&lt;/p&gt;Published as part of &lt;i&gt;Fan, Ximei, Jin, Qing &amp; Li, Houhun, 2008, Seven new species and a checklist of the genus Thecobathra Meyrick from China (Lepidoptera: Yponomeutidae), pp. 13-24 in Zootaxa 1821&lt;/i&gt; on pages 22-23, DOI: &lt;a href="http://zenodo.org/record/183025"&gt;10.5281/zenodo.183025&lt;/a&gt

Thecobathra longisaccata Fan, Jin & Li, 2008, sp. nov.

&lt;i&gt;Thecobathra longisaccata&lt;/i&gt; sp. nov. &lt;p&gt;(Figs. 3, 10)&lt;/p&gt; &lt;p&gt; &lt;b&gt;Type material.&lt;/b&gt; Holotype: ɗ, &lt;b&gt;CHINA:&lt;/b&gt; Ruili [24&deg;00'N, 97&deg;50'E], Yunnan Province, 1000 m, 6.viii.2005, coll. Yingdang Ren, genitalia slide no. FXM06051.&lt;/p&gt; &lt;p&gt; &lt;b&gt;Diagnosis.&lt;/b&gt; The new species can be recognized by the large triangular male valva, an apically rounded large projection near the base of the costa, and the length of the saccus, which exceeds the phallus.&lt;/p&gt; &lt;p&gt; &lt;b&gt;Description.&lt;/b&gt; Adult (Fig. 3): Wing expanse 16.0 mm. Head white, with sparse scales. Antenna with scape white, flagellum white and pale brown alternately. Labial palpus with basal and second segments white, third segment pale brown mixed with white. Thorax and tegula white. Forewing silvery white, somewhat pale yellowish; costal margin with basal 1/8 black, distal half pale yellow; cilia brownish yellow except distal 1/4 black. Hindwing silvery white, tinged with yellowish brown distally; cilia white. Legs white; hind tibia with a yellowish brown dot at end of each side, hind tarsus pale yellow except black at apex.&lt;/p&gt; &lt;p&gt;Male genitalia (Fig. 10): Socius slender, horn shaped, arched on dorsal edge, with a sclerotized tooth apically. Tuba analis membranous. Ventral plate of gnathos large and heart-shaped, blunt and sclerotized apically. Valva subtriangular; uprising, forming a broad right angle ventrally; basal 1/3 broad, almost naked; distal 2/3 triangular, densely setose, oblique on outer margin, pointed at apex; costa curved at middle, with an apically rounded projection basally. Sacculus narrow, indistinct. Saccus long, Y-shaped, anterior 1/3 gradually narrowed, curved distally, rounded at apex. Phallus slender and straight, shorter than saccus, with a row of curved dentation ranging from basal 1/5 to apex.&lt;/p&gt; &lt;p&gt;Female: Unknown.&lt;/p&gt; &lt;p&gt; &lt;b&gt;Distribution.&lt;/b&gt; China (Yunnan).&lt;/p&gt; &lt;p&gt; &lt;b&gt;Etymology.&lt;/b&gt; The specific name is derived from the Latin prefix &lt;i&gt;longi-&lt;/i&gt;, and &lt;i&gt;saccatus&lt;/i&gt;, referring to the saccus, which is longer than the phallus.&lt;/p&gt;Published as part of &lt;i&gt;Fan, Ximei, Jin, Qing &amp; Li, Houhun, 2008, Seven new species and a checklist of the genus Thecobathra Meyrick from China (Lepidoptera: Yponomeutidae), pp. 13-24 in Zootaxa 1821&lt;/i&gt; on pages 17-18, DOI: &lt;a href="http://zenodo.org/record/183025"&gt;10.5281/zenodo.183025&lt;/a&gt

Thecobathra Meyrick 1922

&lt;i&gt;Thecobathra&lt;/i&gt; Meyrick, 1922 &lt;p&gt; &lt;i&gt;Thecobathra&lt;/i&gt; Meyrick, 1922: 553.&lt;/p&gt; &lt;p&gt; Type-species: &lt;i&gt;Thecobathra acropercna&lt;/i&gt; Meyrick, 1922 &lt;i&gt;Pseudocalantica&lt;/i&gt; Friese, 1960: 36.&lt;/p&gt; &lt;p&gt; Type-species: &lt;i&gt;Niphonympha anas&lt;/i&gt; Stringer, 1930&lt;/p&gt; &lt;p&gt; &lt;b&gt;MAP 1.&lt;/b&gt; The distribution of &lt;i&gt;Thecobathra&lt;/i&gt; Meyrick in China&lt;/p&gt;Published as part of &lt;i&gt;Fan, Ximei, Jin, Qing &amp; Li, Houhun, 2008, Seven new species and a checklist of the genus Thecobathra Meyrick from China (Lepidoptera: Yponomeutidae), pp. 13-24 in Zootaxa 1821&lt;/i&gt; on pages 13-14, DOI: &lt;a href="http://zenodo.org/record/183025"&gt;10.5281/zenodo.183025&lt;/a&gt