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From 1994 to 2013, French forensic entomology laboratories investigated 1,093 cases. Larder beetles (Coleoptera: Dermestidae) were observed in 81 (7.5 %) of these cases. To describe and analyze these 81 cases, eight parameters were used: city, location (indoor or outdoor), decay stage (fresh, decay, or dry), dermestid species and instar (adults and/or larvae), presence of living calliphorid larvae, presence of calliphorid pupae or adults, and presence of other necrophagous species. Eight Dermestidae species were observed: Dermestes frischii (42 % of cases), Dermestes undulatus (35.8 %), Dermestes peruvianus (12.3 %), Dermestes lardarius (9.9 %), Dermestes haemorrhoidalis (8.6 %), Dermestes maculatus (7.4 %), Dermestes bicolor (3.7 %), and Dermestes ater (1.2 %). Larder beetles primarily developed on human cadavers in outdoor locations in areas with a dry climate and were never reported in oceanic areas (which are characterized by frequent rainfall and high ambient humidity). The number of dermestid species on a single corpse never exceeded three. Typically, one species was found per corpse. Species differed between indoor and outdoor cases, with D. frischii and D. undulatus dominant in outdoor cases, while D. peruvianus dominant in indoor cases. Calliphoridae was found in 88 % of the cases, while Hydrotaea and Piophilidae were observed 40 % of the time. Regarding Coleoptera, Necrobia spp. (Coleoptera: Cleridae) was observed in 46 % of the cases. Lastly, we observed a typical decomposition pattern, with preferential feeding areas on the face, hands, and feet (i.e., the extremities). Pupation chambers on or inside the bones were not observed.

Most Dermestes species (Coleoptera: Dermestidae) are scavengers during both larval and adult stages, with a preference for dry organic matter. Because of this, Dermestes beetles are potentially useful indicators in forensic investigations concerning skeletonized and mummified human remains. However, there is a paucity of reference developmental data on most forensically relevant Dermestes species. This study analyses the effect of five constant temperatures (15, 20, 25, 30, and 35 °C) on the survival and developmental rates of three of the forensically most relevant dermestids: Dermestes frischii Kugelan, Dermestes maculatus De Geer, and Dermestes undulatus Brahm. Pig skin was used as rearing substrate, to use a substrate as similar as possible to that exploited in nature. Overall, the temperature had a significant effect on the survival and the duration of development, with optimal values at intermediate temperatures. Both D. frischii and D. maculatus showed similar developmental rates and the shortest developmental times at 30 °C, whereas D. undulatus developed faster at lower temperatures. At 15 °C, both D. frischii and D. undulatus did not oviposit, whereas no D. maculatus individuals survived beyond the pupal stage. An inconsistent number of larval instars per individual were observed across different constant temperatures in the three species. The present study aims to provide baseline developmental data for further advances in the potential use of Dermestes beetles as forensic tools in long postmortem interval cases.

•Nesting by bees, wasps and squirrel inside a mummified human corpse in nature.•Case history, autopsy findings, and biological observations are provided.•List of insect found in the corpse is provided and compared with available data.•Other zoological findings are mentioned and briefly discussed. We report, for the first time, a case of nesting by Apis mellifera mellifera (L., 1758) (Insecta: Hymenoptera: Apidae), Vespula vulgaris (L., 1758) (Insecta: Hymenoptera: Vespidae), and Sciurus vulgaris L., 1758 (Mammalia: Rodentia: Sciuridae) inside a mummified human corpse in natural conditions (Lower Silesia province, south-western Poland). A case history, autopsy findings, and biological observations are provided. A list of the insect species found in the corpse is provided and compared with available data. Other zoological findings are mentioned and briefly discussed.

Dermestid beetles (Coleoptera: Dermestidae) are necrophagous insects feeding on mummified carcasses. After six to seven molts, the larvae stop feeding and dig pupation chambers to hide and safely evolve into adults. Such pupation chambers have already been observed on archaeological mammals’ bones, but the attribution and interpretation of these osteological lesions lack experimental evidence in a forensic context. To observe whether dermestid larvae dig pupation chambers in human bones, 20 or 40 Dermestes maculatus (De Geer, 1774) larvae were placed in a dermestarium with different types of bones varying in species (Bos taurus or human), age (adult or immature), and preservation method (fresh or dry). Our results show that dermestid larvae caused multiple lesions, including larval mandible traces on cortical bone, cortical perforations, drilling of pupation chambers, destruction of the trabecular network, and the perforation of cartilage. Bone destruction was mainly observed on aged dry bones, while fresh bones only exhibited soft tissue and superficial cartilage lesions. According to these results, pupation chambers could indicate the simultaneous presence of several corpses at different decomposition stages, or the addition of new corpses while others were already skeletonized. These conclusions are particularly important in the case of mass graves, where chronology is sometimes difficult to establish.

is a significant storage pest which challenging to distinguish it from by external morphological characteristics. This study presents the complete mitochondrial genome of . The mitogenome of spans 15,775 bp and comprises 13 protein-coding genes (PCGs), 22 tRNA genes, two rRNA genes, and an AT-rich region. The nucleotide composition includes A (41.51%), C (14.14%), G (9.03%), and T (35.32%). Phylogenetic analyses by Bayesian inference and maximum-likelihood methods suggest the relationship among three subfamilies: Dermestinae + (Attageninae + Megatominae). Additionally, phylogenetic analysis indicates that is more closely rated to .

The insecticidal activity of the Diatomaceous Earth (DE) of Sig was assessed against the Dermestes haemorrhoidalis, which is the main pest affecting wheat stored in Blida, a central region of Algeria and one of the four cereal regions managed by the Algerian Inter-branch Cereals Office (AICO). The formulation was tested at two different doses: 500 and 1000 ppm against adults of the species. The bioassays were carried out in 1-litre glass jars containing soft wheat with an average moisture content of 60% mixed with diatomaceous earth and maintained at 27°C and 70% of humidity. The effectiveness of the treatment was assessed by recording adult mortality after 2, 7 and 14 days. Sig's diatomite showed significant insecticidal activity against Dermestes haemorrhoidalis after only two days of treatment with both doses 500 and 1000 ppm. After 14 days, average mortality was more than 95% even at 500 ppm. Furthermore, electron microscopy of the diatomite particle from Sig (Algeria) reveals the architecture of the frustule. It shows a porous and brittle siliceous shell made largely of diatomite \"skeletons\". This research work allowed getting insights into the mechanism of action of diatomite on the Dermestes haemorrhoidalis. On the other hand, the identification of diatomite of Sig was performed by X-ray diffraction and infrared.

ABSTRACT Dermestid beetles being low-cost, efficient, and environmentally friendly are commonly used to prepare osteological materials in museums. This study was carried out to produce osteological material from the heads of roe deer, cows, and cats using a Dermestes maculatus (De Geer, 1774) colony and reveal the colony's meat consumption performance in terms of time. In addition, using hydrogen peroxide solution to kill remaining beetles in the cleaned osteological material and determine the whitening and degreasing efficiency of this solution was also aimed. In the study, approximately 10,000 Dermestes maculatus, along with the heads of six roe deer, three cows, and three cats were used. To observe the meat-cleaning performance, the initial and final weights of the heads were measured before they were placed in the beetle colony. All tissues, including eye and brain tissues, of the heads placed in the Dermestes colony were cleaned in one day in cats, two days in roe deer, and three days in cows. In addition, it was observed that the Dermestes colony was not a preference priority when consuming soft tissues such as eyes, brain and muscle. This current manuscript has revealed the advantages of the hydrogen peroxide application in whitening and degreasing bone materials and killing remaining beetles at the end of the process on skull materials cleaned by Dermestes beetles.

•The decomposition process was very short; the remains stage was reached 7 days after death.•A similar composition of carrion entomofauna was found in both sampling years.•Chrysomya albiceps and Cochliomyia macellaria were the primary colonizers of the bodies.•Both blowfly species could provide data for precise estimations of the PMImin.•The dry remains stage was characterized by the adults and larvae of Dermestes maculatus. The succession of carrion fauna and the decomposition stages were studied in summer for two years in open pastures of the Department of Paysandú, Uruguay (32°21′5″S; 58°3′37″). Each year, three pig carcasses (Sus scrofa) were placed in wire mesh cages, 100 m apart from each other. Each carcass was surrounded by pitfall traps, and a modified Malaise trap was placed above. Daily samplings were carried out to collect the insects present in the carcasses and the traps, and body and environmental temperatures were measured. The composition of carrion entomofauna and the decomposition patterns were markedly similar in both sampling years. The decomposition process was rapid, that is, the time to reach the remains stage was 7 days in all treatments, both years. The mosaic nature of decomposition was observed. Both Chrysomya albiceps (Wiedemann) and Cochliomyia macellaria (Fabricius) behaved as primary invaders of the carcasses, although the former species and its larvae were dominant. The first adult blow flies emerged after 6 days. The remains stage was characterized mainly by both adults and larvae of Dermestes maculatus. This preliminary study represents the first contribution to the knowledge of cadaveric succession in Uruguay. Its seasonal replication supports the succession pattern obtained.

More than 4700 nominal family-group names (including names for fossils and ichnotaxa) are nomenclaturally available in the order Coleoptera. Since each family-group name is based on the concept of its type genus, we argue that the stability of names used for the classification of beetles depends on accurate nomenclatural data for each type genus. Following a review of taxonomic literature, with a focus on works that potentially contain type species designations, we provide a synthesis of nomenclatural data associated with the type genus of each nomenclaturally available family-group name in Coleoptera. For each type genus the author(s), year of publication, and page number are given as well as its current status (i.e., whether treated as valid or not) and current classification. Information about the type species of each type genus and the type species fixation (i.e., fixed originally or subsequently, and if subsequently, by whom) is also given. The original spelling of the family-group name that is based on each type genus is included, with its author(s), year, and stem. We append a list of nomenclaturally available family-group names presented in a classification scheme. Because of the importance of the Principle of Priority in zoological nomenclature, we provide information on the date of publication of the references cited in this work, when known. Several nomenclatural issues emerged during the course of this work. We therefore appeal to the community of coleopterists to submit applications to the International Commission on Zoological Nomenclature (henceforth “Commission”) in order to permanently resolve some of the problems outlined here. The following changes of authorship for type genera are implemented here (these changes do not affect the concept of each type genus): CHRYSOMELIDAE: Fulcidax Crotch, 1870 (previously credited to “Clavareau, 1913”); CICINDELIDAE: Euprosopus W.S. MacLeay, 1825 (previously credited to “Dejean, 1825”); COCCINELLIDAE: Alesia Reiche, 1848 (previously credited to “Mulsant, 1850”); CURCULIONIDAE: Arachnopus Boisduval, 1835 (previously credited to “Guérin-Méneville, 1838”); ELATERIDAE: Thylacosternus Gemminger, 1869 (previously credited to “Bonvouloir, 1871”); EUCNEMIDAE: Arrhipis Gemminger, 1869 (previously credited to “Bonvouloir, 1871”), Mesogenus Gemminger, 1869 (previously credited to “Bonvouloir, 1871”); LUCANIDAE: Sinodendron Hellwig, 1791 (previously credited to “Hellwig, 1792”); PASSALIDAE: Neleides Harold, 1868 (previously credited to “Kaup, 1869”), Neleus Harold, 1868 (previously credited to “Kaup, 1869”), Pertinax Harold, 1868 (previously credited to “Kaup, 1869”), Petrejus Harold, 1868 (previously credited to “Kaup, 1869”), Undulifer Harold, 1868 (previously credited to “Kaup, 1869”), Vatinius Harold, 1868 (previously credited to “Kaup, 1869”); PTINIDAE: Mezium Leach, 1819 (previously credited to “Curtis, 1828”); PYROCHROIDAE: Agnathus Germar, 1818 (previously credited to “Germar, 1825”); SCARABAEIDAE: Eucranium Dejean, 1833 (previously “Brullé, 1838”). The following changes of type species were implemented following the discovery of older type species fixations (these changes do not pose a threat to nomenclatural stability): BOLBOCERATIDAE: Bolbocerus bocchus Erichson, 1841 for Bolbelasmus Boucomont, 1911 (previously Bolboceras gallicum Mulsant, 1842); BUPRESTIDAE: Stigmodera guerinii Hope, 1843 for Neocuris Saunders, 1868 (previously Anthaxia fortnumi Hope, 1846), Stigmodera peroni Laporte & Gory, 1837 for Curis Laporte & Gory, 1837 (previously Buprestis caloptera Boisduval, 1835); CARABIDAE: Carabus elatus Fabricius, 1801 for Molops Bonelli, 1810 (previously Carabus terricola Herbst, 1784 sensu Fabricius, 1792); CERAMBYCIDAE: Prionus palmatus Fabricius, 1792 for Macrotoma Audinet-Serville, 1832 (previously Prionus serripes Fabricius, 1781); CHRYSOMELIDAE: Donacia equiseti Fabricius, 1798 for Haemonia Dejean, 1821 (previously Donacia zosterae Fabricius, 1801), Eumolpus ruber Latreille, 1807 for Euryope Dalman, 1824 (previously Cryptocephalus rubrifrons Fabricius, 1787), Galeruca affinis Paykull, 1799 for Psylliodes Latreille, 1829 (previously Chrysomela chrysocephala Linnaeus, 1758); COCCINELLIDAE: Dermestes rufus Herbst, 1783 for Coccidula Kugelann, 1798 (previously Chrysomela scutellata Herbst, 1783); CRYPTOPHAGIDAE: Ips caricis G.-A. Olivier, 1790 for Telmatophilus Heer, 1841 (previously Cryptophagus typhae Fallén, 1802), Silpha evanescens Marsham, 1802 for Atomaria Stephens, 1829 (previously Dermestes nigripennis Paykull, 1798); CURCULIONIDAE: Bostrichus cinereus Herbst, 1794 for Crypturgus Erichson, 1836 (previously Bostrichus pusillus Gyllenhal, 1813); DERMESTIDAE: Dermestes trifasciatus Fabricius, 1787 for Attagenus Latreille, 1802 (previously Dermestes pellio Linnaeus, 1758); ELATERIDAE: Elater sulcatus Fabricius, 1777 for Chalcolepidius Eschscholtz, 1829 (previously Chalcolepidius zonatus Eschscholtz, 1829); ENDOMYCHIDAE: Endomychus rufitarsis Chevrolat, 1835 for Epipocus Chevrolat, 1836 (previously Endomychus tibialis Guérin-Méneville, 1834); EROTYLIDAE: Ips humeralis Fabricius, 1787 for Dacne Latreille, 1797 (previously Dermestes bipustulatus Thunberg, 1781); EUCNEMIDAE: Fornax austrocaledonicus Perroud & Montrouzier, 1865 for Mesogenus Gemminger, 1869 (previously Mesogenus mellyi Bonvouloir, 1871); GLAPHYRIDAE: Melolontha serratulae Fabricius, 1792 for Glaphyrus Latreille, 1802 (previously Scarabaeus maurus Linnaeus, 1758); HISTERIDAE: Hister striatus Forster, 1771 for Onthophilus Leach, 1817 (previously Hister sulcatus Moll, 1784); LAMPYRIDAE: Ototreta fornicata E. Olivier, 1900 for Ototreta E. Olivier, 1900 (previously Ototreta weyersi E. Olivier, 1900); LUCANIDAE: Lucanus cancroides Fabricius, 1787 for Lissotes Westwood, 1855 (previously Lissotes menalcas Westwood, 1855); MELANDRYIDAE: Nothus clavipes G.-A. Olivier, 1812 for Nothus G.-A. Olivier, 1812 (previously Nothus praeustus G.-A. Olivier, 1812); MELYRIDAE: Lagria ater Fabricius, 1787 for Enicopus Stephens, 1830 (previously Dermestes hirtus Linnaeus, 1767); NITIDULIDAE: Sphaeridium luteum Fabricius, 1787 for Cychramus Kugelann, 1794 (previously Strongylus quadripunctatus Herbst, 1792); OEDEMERIDAE: Helops laevis Fabricius, 1787 for Ditylus Fischer, 1817 (previously Ditylus helopioides Fischer, 1817 [sic]); PHALACRIDAE: Sphaeridium aeneum Fabricius, 1792 for Olibrus Erichson, 1845 (previously Sphaeridium bicolor Fabricius, 1792); RHIPICERIDAE: Sandalus niger Knoch, 1801 for Sandalus Knoch, 1801 (previously Sandalus petrophya Knoch, 1801); SCARABAEIDAE: Cetonia clathrata G.-A. Olivier, 1792 for Inca Lepeletier & Audinet-Serville, 1828 (previously Cetonia ynca Weber, 1801); Gnathocera vitticollis W. Kirby, 1825 for Gnathocera W. Kirby, 1825 (previously Gnathocera immaculata W. Kirby, 1825); Melolontha villosula Illiger, 1803 for Chasmatopterus Dejean, 1821 (previously Melolontha hirtula Illiger, 1803); STAPHYLINIDAE: Staphylinus politus Linnaeus, 1758 for Philonthus Stephens, 1829 (previously Staphylinus splendens Fabricius, 1792); ZOPHERIDAE: Hispa mutica Linnaeus, 1767 for Orthocerus Latreille, 1797 (previously Tenebrio hirticornis DeGeer, 1775). The discovery of type species fixations that are older than those currently accepted pose a threat to nomenclatural stability (an application to the Commission is necessary to address each problem): CANTHARIDAE: Malthinus Latreille, 1805, Malthodes Kiesenwetter, 1852; CARABIDAE: Bradycellus Erichson, 1837, Chlaenius Bonelli, 1810, Harpalus Latreille, 1802, Lebia Latreille, 1802, Pheropsophus Solier, 1834, Trechus Clairville, 1806; CERAMBYCIDAE: Callichroma Latreille, 1816, Callidium Fabricius, 1775, Cerasphorus Audinet-Serville, 1834, Dorcadion Dalman, 1817, Leptura Linnaeus, 1758, Mesosa Latreille, 1829, Plectromerus Haldeman, 1847; CHRYSOMELIDAE: Amblycerus Thunberg, 1815, Chaetocnema Stephens, 1831, Chlamys Knoch, 1801, Monomacra Chevrolat, 1836, Phratora Chevrolat, 1836, Stylosomus Suffrian, 1847; COLONIDAE: Colon Herbst, 1797; CURCULIONIDAE: Cryphalus Erichson, 1836, Lepyrus Germar, 1817; ELATERIDAE: Adelocera Latreille, 1829, Beliophorus Eschscholtz, 1829; ENDOMYCHIDAE: Amphisternus Germar, 1843, Dapsa Latreille, 1829; GLAPHYRIDAE: Anthypna Eschscholtz, 1818; HISTERIDAE: Hololepta Paykull, 1811, Trypanaeus Eschscholtz, 1829; LEIODIDAE: Anisotoma Panzer, 1796, Camiarus Sharp, 1878, Choleva Latreille, 1797; LYCIDAE: Calopteron Laporte, 1838, Dictyoptera Latreille, 1829; MELOIDAE: Epicauta Dejean, 1834; NITIDULIDAE: Strongylus Herbst, 1792; SCARABAEIDAE: Anisoplia Schönherr, 1817, Anticheira Eschscholtz, 1818, Cyclocephala Dejean, 1821, Glycyphana Burmeister, 1842, Omaloplia Schönherr, 1817, Oniticellus Dejean, 1821, Parachilia Burmeister, 1842, Xylotrupes Hope, 1837; STAPHYLINIDAE: Batrisus Aubé, 1833, Phloeonomus Heer, 1840, Silpha Linnaeus, 1758; TENEBRIONIDAE: Bolitophagus Illiger, 1798, Mycetochara Guérin-Méneville, 1827. Type species are fixed for the following nominal genera: ANTHRIBIDAE: Decataphanes gracilis Labram & Imhoff, 1840 for Decataphanes Labram & Imhoff, 1840; CARABIDAE: Feronia erratica Dejean, 1828 for Loxandrus J.L. LeConte, 1853; CERAMBYCIDAE: Tmesisternus oblongus Boisduval, 1835 for Icthyosoma Boisduval, 1835; CHRYSOMELIDAE: Brachydactyla annulipes Pic, 1913 for Pseudocrioceris Pic, 1916, Cassida viridis Linnaeus, 1758 for Evaspistes Gistel, 1856, Ocnoscelis cyanoptera Erichson, 1847 for Ocnoscelis Erichson, 1847, Promecotheca petelii Guérin-Méneville, 1840 for Promecotheca Guérin- Méneville, 1840; CLERIDAE: Attelabus mollis Linnaeus, 1758 for Dendroplanetes Gistel, 1856; CORYLOPHIDAE: Corylophus marginicollis J.L. LeConte, 1852 for Corylophodes A. Matthews, 1885; CURCULIONIDAE: Hoplorhinus melanocephalus Chevrolat, 1878 for Hoplorhinus Chevrolat, 1878; Sonnetius binarius Casey, 1922 for Sonnetius Casey, 1922; ELATERIDAE: Pyrophorus melanoxanthus Candèze, 1865 for Alampes Champion, 1896; PHYCOSECIDAE: Phycosecis litoralis P