scholarly journals A fossil water measurer (Insecta, Hemiptera, Hydrometridae) from the Paleocene/Eocene of Denmark and its phylogenetic relationships

1982 ◽  
Vol 30 ◽  
pp. 91-96
Author(s):  
N. Møller Andersen

The first fossil species of hydrometrid bugs, Eocenometra danica n.gen., n.sp., is described from deposits of Upper Paleocene/Lower Eocene age ( c. 50 million years) from northern Jutland, Denmark. The extinct form is compared with extant genera of the family Hydrometridae and its phylogenetic relationships are discussed. Paleoecological and biogeographical notes are included.

2019 ◽  
Vol 94 (3) ◽  
pp. 568-579
Author(s):  
Alexander O. Averianov

AbstractKazachostylops occidentalis Nesov, 1987b, based on partial maxilla and dentary from the upper Paleocene Zhylga locality in South Kazakhstan, is redescribed. A new phylogenetic hypothesis of Arctostylopida is proposed based on phylogenetic analysis of 26 characters and 17 taxa. Kazachostylops is recovered as a sister taxon to the Arctostylopinae, the advanced clade of Asian and North American arctostylopids characterized by pseudohypocone on upper molars and reduced trigonid of lower molars, with the ectolophid being attached labial on the trigonid. Kazachostylops differs from more basal arctostylopids (Asiostylops, Allostylops, Bothriostylops, and Wanostylops) by higher-crowned molars, M1–3 metaconule absent, m1–3 entoconid connected with ectolophid by entolophid, and m2 wider than m1 and m3. Principal component analyses of the upper and lower dentition of arctostylopids show great distinctness of Kazachostylops from other members of the group. The arctostylopid taxa are reviewed, and the new genus Enantiostylops is erected for ‘Sinostylops’ progressus Tang and Yan, 1976 from the lower Eocene of China, because of uniquely concave parastylar area on upper molars.UUID: http://zoobank.org/a46d8f29-fd73-4e59-88dc-fcc55b12d1d3


Author(s):  
J. Alan Holman

In both Europe and North America, modern herpetological families and genera became established quite early in the Cenozoic, and modern species occurred as early as the Miocene. Because of deteriorating climates that began late in the Eocene, a marked decrease in herpetological diversity occurred in the Oligocene in both continents. However, both areas became herpetologically enriched in the Miocene. In post-Miocene times Europe was isolated from Africa and warm areas in the east by the Mediterranean Sea and eastern mountain ranges, and a depauperate herpetofauna developed there that continued into recent times. In North America, however, with its vast, accessible southern land mass, the richness of the Miocene herpetofauna (with the exception of several archaic colubrid genera [Parmley and Holman, 1995] that became extinct in the the Miocene) persisted into modern times. The following discussion of changes in the European herpetofauna in the Cenozoic era has been synthesized from Auge (1986), Ballón (1991a), Bailon ct al. (1988), Barbadillo et al. (1997), Crochet et al. (1981), Estes (1981, 1982, 1983), Fritz (1995), Holman (1995c), Milncr (1986), Milner et al. (1982), Mlynarski (1976), Rage (1984a, 1984c, 1986, 1993), Rage and Auge (1993), Rage and Ford (1980), Roček (1994), Sanchiz. (1977b, in press), Sanchiz and Mlynarski (1979), Sanchiz and Roček (1996), Spinar (1972), Szyndlar (1984, 1991b, 1991c), and Szyndlar and Bohme (1993). Because of the high probability that herpetological fossils have been identified correctly at the family level, herpetological families arc used here to reflect the taxonomic diversity of the European herpetofauna from the Paleocene through the Pliocene. In a following section, the earliest appearance of herpetological genera and species in the European Tertiary arc discussed. Extinct families are prefixed with an asterisk (*). Families that became extinct in Europe in the Cenozoic but presently occur elsewhere are prefixed with a number sign (#). Two primitive, extinct, presumably permanently aquatic salamander families, me *Albanerpetontidae and *Batrachosauroididae (the latter also known from the Tertiary of North America) made limited appearances in the Cenozoic of Europe. The *Albanerpetontidae occurred only in the Middle Miocene (having reappeared from the Cretaceous), and the *Batrachosauroididae occurred from the Upper Paleocene to the Lower Eocene.


Geosciences ◽  
2019 ◽  
Vol 9 (12) ◽  
pp. 514 ◽  
Author(s):  
Maxim V. Nabozhenko

The fossil record of Tenebrionidae (excluding the Quartenary) is presented. In total, 122 fossil species, clearly belonging to the family, are known; some beetles were determined only to genus; 78 genera are listed in the fossil record, including 29 extinct genera. The great diversity of tenebrionids occurs in the Lower Cretaceous Lagerstätte of China (Yixian Formation), Middle Paleocene of France (Menat), Lower Eocene deposits of Germany (Geiseltal), Upper Eocene Baltic amber (Eastern Europe), Upper Eocene deposits of Florissant Formation (USA) and Miocene (Dominican amber). Tenebrionids of the following major lineages, including seven subfamilies, are currently known in the fossil record. These include the lagrioid branch (Lagriinae, Nilioninae), pimelioid branch (Pimeliinae), and tenebrioid branch (Alleculinae, Tenebrioninae, Diaperinae, Stenochiinae). The importance of the fossil record for evolutionary reconstructions and phylogenetic patterns is discussed. The oldest Jurassic and Early Cretaceous darkling beetles of the tenebrionoid branch consist of humid-adapted groups from the extant tribes Alleculini, Ctenopodiini (Alleculinae), and Alphitobiini (Tenebrioninae). Thus, paleontological evidence suggests that differentiation of the family started at least by the Middle Jurassic but does not indicate that xerophilic darkling beetles differentiated much earlier than mesophilic groups.


2021 ◽  
pp. 1-15
Author(s):  
Juan López-Gappa ◽  
Leandro M. Pérez ◽  
Ana C.S. Almeida ◽  
Débora Iturra ◽  
Dennis P. Gordon ◽  
...  

Abstract Bryozoans with calcified frontal shields formed by the fusion of costae, collectively constituting a spinocyst, are traditionally assigned to the family Cribrilinidae. Today, this family is regarded as nonmonophyletic. In the Argentine Cenozoic, cribrilinids were until recently represented by only two fossil species from the Paleocene of Patagonia. This study describes the first fossil representatives of Jolietina and Parafigularia: J. victoria n. sp. and P. pigafettai n. sp., respectively. A fossil species of Figularia, F. elcanoi n. sp., is also described. The material comes from the early Miocene of the Monte León and Chenque formations (Patagonia, Argentina). For comparison, we also provide redescriptions of the remaining extant species of Jolietina: J. latimarginata (Busk, 1884) and J. pulchra Canu and Bassler, 1928a. The systematic position of some species previously assigned to Figularia is here discussed. Costafigularia n. gen. is erected, with Figularia pulcherrima Tilbrook, Hayward, and Gordon, 2001 as type species. Two species previously assigned to Figularia are here transferred to Costafigularia, resulting in C. jucunda n. comb. and C. tahitiensis n. comb. One species of Figularia is reassigned to Vitrimurella, resulting in V. ampla n. comb. The family Vitrimurellidae is here reassigned to the superfamily Cribrilinoidea. The subgenus Juxtacribrilina is elevated to genus rank. Inferusia is regarded as a subjective synonym of Parafigularia. Parafigularia darwini Moyano, 2011 is synonymized with I. taylori Kuklinski and Barnes, 2009, resulting in Parafigularia taylori n. comb. Morphological data suggest that these genera comprise different lineages, and a discussion on the disparities among cribrilinid (sensu lato) spinocysts is provided. UUID: http://zoobank.org/215957d3-064b-47e2-9090-d0309f6c9cd8


2002 ◽  
Vol 11 (2) ◽  
pp. 169-174 ◽  
Author(s):  
Peggy S. M. Hill ◽  
Cara Hoffart ◽  
Mark Buchheim

2005 ◽  
Vol 26 (2) ◽  
pp. 139-147 ◽  
Author(s):  
Francisca do Val ◽  
Paulo Nuin

AbstractThe systematics and phylogenetic relationships of the family Leptodactylidae are controversial as is the intrafamilial phylogeny of the leptodactylids. Here we analyze the relationships of the leptodactylid subfamily Hylodinae. This subfamily has been considered to be monophyletic and composed of three genera, Hylodes, Crossodactylus and Megaelosia. In the present study 49 characters were used, based on different studies on Leptodactylidae phylogeny. Maximum parsimony methods with unweighted and successively weighted characters were used to estimate the phylogeny of the Hylodinae. Upon analysis, the data provided further evidence of the monophyletic status of the three genera, with Megaelosia being the basal genus and the other two genera being sister taxa. The analysis with successive weighting results in a more resolved topology of the species subgroups of the genus Hylodes and separates this genus from Crossodactylus and confirms that the hylodines are monophyletic.


Zootaxa ◽  
2021 ◽  
Vol 4990 (1) ◽  
pp. 192-200
Author(s):  
SIMONE MARIA DE ALBUQUERQUE LIRA ◽  
CYNTHIA DAYANNE MELLO DE LIMA ◽  
IGOR DE ÁVILA TEIXEIRA ◽  
RALF SCHWAMBORN

The objective of this paper is to describe and illustrate the first zoeal stage of the largest land crab of the Tropical Atlantic, Johngarthia lagostoma (Milne Edwards, 1837) (Brachyura: Gecarcinidae). A larval description of J. lagostoma was previously not available. Larvae were obtained from ovigerous females on Rocas Atoll and Fernando de Noronha Archipelago, Brazil. Twenty larvae were randomly chosen to be dissected and described in detail, while 40 others (20 larvae from each island) were measured only. The published description of the congener J. planatus (Stimpson, 1860) larvae was used for a comparison of larval morphology. Some morphological differences between the first zoeal stage of these two species were: The absence or presence of a simple shorter seta on antennule, number of the minute terminal spines on the antenna, setation of the coxal endite of the maxilla, exopod unsegmented of the first and second maxilliped, and a single mid-dorsal seta on first pleonite. These results and differences observed between these species can assist in studies on phylogenetic relationships within the Family Gecarcinidae MacLeay, 1838, as well as in the identification of the larvae of J. Lagostoma in plankton samples from the tropical Atlantic.  


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