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Thursday, November 14th, 2019

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    9:38a
    [Herpetology • 2019] Acanthosaura tongbiguanensis • A New Species of the Genus Acanthosaura (Squamata, Agamidae) from Yunnan, China

    Acanthosaura tongbiguanensis
     Liu & Rao, 2019


    Abstract
    A new species of Acanthosaura from Yunnan, China is described based on unique morphometric and meristic external characters and a very distinctive color pattern. The fourteenth species recorded of this genus, Acanthosaura tongbiguanensis sp. nov., was previously considered A. lepidogaster although it more closely resembles A. crucigera. It can be separated from all other species of the genus by having different numbers of subdigital lamellae on the fourth finger and toe, and a different shape of the black eye patch. The new species differs genetically from investigated congeners by percentage distance of 14.46% to 23.27% (cytochrome b gene).

    Keywords: Acanthosaura crucigera, Dehong, Acanthosaura lepidogaster, Tongbiguan


    Figure 3. Adult male holotype (KIZL201804) of  Acanthosaura tongbiguanensis sp. nov. in life
     A lateral view of the head B dorsal view of the body C dorsal view of the head D lateral view of the body E ventral view of the head F ventral view of the body.


    Figure 4. Adult female paratype (KIZL201805) of  Acanthosaura tongbiguanensis sp. nov. in life
     A lateral view of the head B dorsal view of the body C dorsal view of the head D lateral view of the body E ventral view of the head F ventral view of the body.  


    Figure 7. Comparison of three different types of eye patch A  Acanthosaura tongbiguanensis sp. nov. B A. lepidogaster C A. nataliae.  


     Acanthosaura tongbiguanensis sp. nov. 
    Acanthosaura lepidogaster: Zhao et al. 1999: 82–85.
    Acanthosaura lepidogaster: Yang and Rao 2008: 186–187.

    Diagnosis: 
    A medium-sized (maximum SVL 115.6 mm) agamid lizard with two pairs of spines: postorbital (supraciliary) spines and spines on occiput between tympanum and nuchal crest; tympanum naked; moderately developed gular pouch; scales on flanks randomly intermixed with medium and large scales; nuchal crest present and strongly developed; diastema between the nuchal and dorsal crests present; dorsal crest slightly developed, composed of enlarged, pointed scales beginning at shoulder region and decreasing regularly in size; tail 1.56–1.85 times SVL; black nuchal collar present; black eye patch present; black oblique folds anterior to the fore limb insertions present.

    The new species can be separated from all congeners by having different numbers of subdigital lamellae on the fourth finger (19–21) and toe (25–28), and a different shape of the black eye patch, that extends from posterior margin of nostrils through orbit posteriorly and downwards beyond the posterior end of the tympanum but neither meeting the diamond shaped black nuchal collar on nape nor black oblique humeral fold.
    ....

    Etymology: The name refers to Tongbiguan Nature Reserve, the locality where the new species was found.

    Figure 10.  Acanthosaura tongbiguanensis sp. nov. A live adult male on the ground B live adult female on a leaf C live adult female asleep on a branch D live juvenile asleep on branches and leaves.


    Figure 9. Habitat at the type locality of  Acanthosaura tongbiguanensis sp. nov., Tongbiguan Township, Yingjiang County, Dehong Autonomous Prefecture, Yunnan, China
    A distant view B close view.

    Distribution: Acanthosaura tongbiguanensis sp. nov. is only recorded in Tongbiguan Nature Reserve including Yingjiang County, Longchuan County and Ruili City, the border region with northern Myanmar in western Yunnan, China, so it probably occurs in northern Myanmar.

    Natural history: The type series of Acanthosaura tongbiguanensis sp. nov. was collected at night while they were asleep on small trees in a primordial forest. However, we suppose that they forage for food on the ground during the day. At the type locality we found four other species of reptiles, namely Cyrtodactylus khasiensis (Jerdon, 1870), Pseudocalotes kakhienensis (Anderson, 1879); P. microlepis (Boulenger, 1887); Trimeresurus yingjiangensis Chen et al., 2019; and seven species of amphibians, Leptobrachella yingjiangensis (Yang et al., 2018); Limnonectes longchuanensis Suwannapoom et al., 2016; Megophrys feii Yang et al., 2018; M. glandulosa Fei et al., 1990; Raorchestes longchuanensis (Yang & Li, 1978); Theloderma moloch (Annandale, 1912); Zhangixalus smaragdinus (Blyth, 1852).



     Shuo Liu and Dingqi Rao. 2019. A New Species of the Genus Acanthosaura from Yunnan, China (Squamata, Agamidae).  ZooKeys. 888: 105-132. DOI: 10.3897/zookeys.888.38491

    10:04a
    [PaleoEntomology • 2019] Angimordella burmitina • Pollination of Cretaceous Flowers

    Angimordella burmitina 
    Bao, Wang, Li & Dilcher, 2019

    The color and morphology of flowers are artistic only. Illustration: Ding-hau Yang. 

    Significance: 
    Since Darwin, insect pollination was thought to be a key contributor to the Cretaceous radiation of angiosperms. Both insects and angiosperms were common during the mid-Cretaceous, but direct evidence for a Cretaceous insect-angiosperm pollination mode was until now absent. Here, we report a specialized beetle-angiosperm pollination mode preserved in Burmese amber where a tumbling flower beetle is carrying tricolpate pollen grains that belongs to the eudicots that comprise the majority of extant angiosperm species. Our study provides direct evidence of insect pollination of Cretaceous flowers, which is further supported by the flower-visiting body shape, specialized pollen-feeding mouthparts, and zoophilous pollen grains. These findings demonstrate that insect pollination of flowering plants was well established 99 million years ago.

    Abstract
    Insect pollination of flowering plants (angiosperms) is responsible for the majority of the world’s flowering plant diversity and is key to the Cretaceous radiation of angiosperms. Although both insects and angiosperms were common by the mid-Cretaceous, direct fossil evidence of insect pollination is lacking. Direct evidence of Cretaceous insect pollination is associated with insect-gymnosperm pollination. Here, we report a specialized beetle-angiosperm pollination mode from mid-Cretaceous Burmese amber (99 mega-annum [Ma]) in which a tumbling flower beetle (Mordellidae), Angimordella burmitina gen. et sp. nov., has many tricolpate pollen grains attached. A. burmitina exhibits several specialized body structures for flower-visiting behavior including its body shape and pollen-feeding mouthparts revealed by X-ray microcomputed tomography (micro-CT). The tricolpate pollen in the amber belongs to the eudicots that comprise the majority of extant angiosperm species. These pollen grains exhibit zoophilous pollination attributes including their ornamentation, size, and clumping characteristics. Tricolpate pollen grains attached to the beetle’s hairs are revealed by confocal laser scanning microscopy, which is a powerful tool for investigating pollen in amber. Our findings provide direct evidence of insect pollination of Cretaceous angiosperms, extending the range insect-angiosperm pollination association by at least 50 million years. Our results support the hypothesis that specialized insect pollination modes were present in eudicots 99 million years ago.

    Keywords: amber, insect, angiosperm, pollen, paleoecology


      Fig. 2. Angimordella burmitina and tricolpate pollen grains.
     (A) Habitus. Pollen grains attached to the body are indicated by red dots, unattached are indicated by yellow dots, clumped pollen are indicated by blue squares. (B−H) Locations are highlighted in A. (B and C) Pollen grains near the body. Yellow arrows point to colpi. (D and E) Pollen grains on the body. (F−H) Clumped pollen grains. (G and H) Locations are highlighted in F and G, respectively. Blue arrows point to colpi.

    Family Mordellidae Latreille, 1802.
    Subfamily Mordellinae Latreille, 1802.

    Angimordella burmitina gen. et sp. nov.

    Etymology: The generic name is derived from the Latin prefix “angi” (referring to angiosperm) and the genus Mordella Linnaeus. The specific name is derived from Latin “Burmitina,” referring to the mineralogical name of Burmese amber.

    Holotype :NIGP171315 (Fig. 1), a complete beetle with left side visible but its right side covered by abundant microbubbles. A thrip is near the maxillary palpi of the beetle on the left side.

    Horizon and Locality: Mid-Cretaceous (∼99 Ma); Burmese amber, from the Hukawng Valley, Kachin State, Myanmar.

    Diagnosis: Body small, with pronotum and elytra with wrinkles or ridges dorsally; antennae serrate; mesotibiae and metatibiae without any kind of ridge including subapical one; pygidium not well developed, shorter than 1/2 of last abdominal sternite.

     Fig. 3. Ecological reconstruction of Angimordella burmitina. These tumbling flower beetles are feeding on eudicot flowers.
    The color and morphology of flowers are artistic only. 
    Illustration: Ding-hau Yang. 


    Tong Bao, Bo Wang, Jianguo Li, and David Dilcher. 2019. Pollination of Cretaceous Flowers. PNAS. DOI: 10.1073/pnas.1916186116

    New fossil pushes back physical evidence of insect pollination to 99 million years ago  phys.org/news/2019-11-fossil-physical-evidence-insect-pollination.html via @physorg_com
    A Specialized Beetle-Angiosperm Pollination Mode from mid-Cretaceous Burmese Amber

    10:22a
    [Crustacea • 2019] Paguroids (Decapoda: Anomura: Diogenidae and Paguridae) of the Remote Oceanic Archipelago Trindade and Martin Vaz, off southeast Brazil, with New Records, Description of Three New Species and Zoogeographical Notes

    Iridopagurus martinvaz 
     Lima, Tavares & de Mendonça, 2019


    Abstract
    Trindade and Martin Vaz (TMV) is a highly isolated, oceanic volcanic archipelago located some 1200 km off the Brazilian coast and about 4200 km away from the nearest African coast. For almost 100 years Calcinus tibicen (Herbst, 1791) was the only hermit crab species known from TMV. From 2012 to 2018, 263 daytime SCUBA diving and intertidal samplings conducted at TMV yielded 1075 paguroid specimens in 10 species, three of which are established herein as new species: Iridopagurus martinvaz sp. nov., Nematopagurus micheleae sp. nov., and Pagurus carmineus sp. nov. Iridopagurus margaritensis García-Gómez, 1983, and Phimochirus leurocarpus McLaughlin, 1981, both only known from the northern hemisphere, are recorded for the first time from the southwestern Atlantic. Opportunity was taken herein to include hitherto unreported or little known specimens from along the Vitória-Trindade Seamount Chain, namely, Dardanus venosus H. Milne Edwards, 1848, Nematopaguroides pusillus Forest & de Saint Laurent, 1968, Pagurus provenzanoi Forest & de Saint Laurent, 1968, and Phimochirus holthuisi (Provenzano, 1961). The lectotype of Pagurus venosus H. Milne Edwards, 1848 is designated as the neotype for the obscure Pagurus arrosor divergens Moreira, 1905, which thus becomes an objective junior synonym of the former. A list of all paguroid species known from the tropical southern-central Atlantic oceanic archipelagoes and islands (Ascension, Cape Verde, Fernando de Noronha, Gulf of Guinea, Rocas Atoll, Saint Helena, Trindade and Martin Vaz) with their gross distribution in the Atlantic Ocean is provided. Investigation on the existence of patterns of geographic distribution for the paguroid fauna of the tropical southern-central Atlantic oceanic islands showed that 70% percent of the paguroids from TMV are western Atlantic in origin and 30% endemic. No amphi-Atlantic paguroid species are known from TMV. Conversely, the affinity of Ascension’s (33%) and Saint Helena’s (50%) paguroids is with the eastern Atlantic; no western Atlantic paguroids have been reported from these two islands so far. Exploration on the existence of trends of correlation between islands area and species richness through the Spearman’s coefficient of correlation showed that the patterns in the number of paguroid species cannot be explained by variation in island area alone (rs = 0.4728; p = 0.28571).

    Keywords: Crustacea, Vitória-Trindade Seamount Chain, species-area relationships, hermit crabs, Crustacea, Paguroidea


     Trindade and Martin Vaz Archipelago (TMV):
    A—Position of the TMV relative to the Brazilian continental coastline and Vitória-Trindade Seamount Chain, and isobath curves around TMV; B—Trindade Island viewed from distance; C—Martin Vaz Islands viewed from distance; D–G—Trindade Island; D—rocky-sandy beach near Parcel das Tartarugas, partly exposed at low tide; E—artificial reef substrate (ARS) being deployed on hard bottom composed of large boulders among patches of sand and calcareous algae; F—mixed hard bottom characterised by numerous nodules of calcareous algae; G—irregular hard limestone bottom. A, adapted from Perreira-Filho et al. (2011); photographs by J.B. Mendonça

    Daniel Lima, Marcos Tavares and Joel Braga Jr. de Mendonça. 2019.  Paguroids (Decapoda: Anomura: Diogenidae and Paguridae) of the Remote Oceanic Archipelago Trindade and Martin Vaz, off southeast Brazil, with New Records, Description of Three New Species and Zoogeographical Notes. Zootaxa. 4694(1); 1–63. DOI: 10.11646/zootaxa.4694.1.1

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