taxonID	type	format	identifier	references	title	description	created	creator	contributor	publisher	audience	source	license	rightsHolder	datasetID
0387774D3A769C6DFEB2FB16FECAFEAF.taxon	http://purl.org/dc/dcmitype/StillImage	image/png	https://zenodo.org/record/14806399/files/figure.png	https://doi.org/10.5281/zenodo.14806399	Figure 1. Phylogeny of Apiomerini based on morphology and habitus of generic representatives. The topology shown is the strict consensus of the two shortest trees derived from the equal weights (EW) analysis. The two fundamental trees only differ in relationships amongst three outgroups (Harpactorini). The implied weights analysis (IW; k = 1000) resulted in one tree with identical topology to one of the two fundamental EW trees (see inset; only relationships amongst out-group Harpactorini shown). Numbers above branches are symmetrical resampling frequencies (GC) of the EW analysis, and numbers in square brackets are GC values of the IW analysis. Apiomerus (light grey) and Heniartes (dark grey) clades are indicated. Habitus images are originals, and the line drawing of Apicrenus fossilis is modified from Maldonado et al. (1993).	Figure 1. Phylogeny of Apiomerini based on morphology and habitus of generic representatives. The topology shown is the strict consensus of the two shortest trees derived from the equal weights (EW) analysis. The two fundamental trees only differ in relationships amongst three outgroups (Harpactorini). The implied weights analysis (IW; k = 1000) resulted in one tree with identical topology to one of the two fundamental EW trees (see inset; only relationships amongst out-group Harpactorini shown). Numbers above branches are symmetrical resampling frequencies (GC) of the EW analysis, and numbers in square brackets are GC values of the IW analysis. Apiomerus (light grey) and Heniartes (dark grey) clades are indicated. Habitus images are originals, and the line drawing of Apicrenus fossilis is modified from Maldonado et al. (1993).	2016-07-10	Forero, Dimitri;Weirauch, Christiane		Zenodo	biologists	Forero, Dimitri;Weirauch, Christiane			
0387774D3A769C6DFEB2FB16FECAFEAF.taxon	http://purl.org/dc/dcmitype/StillImage	image/png	https://zenodo.org/record/14806401/files/figure.png	https://doi.org/10.5281/zenodo.14806401	Figure 2. Predatory and oviposition behaviours in Apiomerus flaviventris from California, USA (A–C), and in Heniartes spp. from Trinidad (D, E) and French Guiana (F): A, bee assassin with honey bee; B, female with resin-coated abdominal venter; C, resin transfer from abdominal storage area to eggs; D, female depositing eggs on Melastomataceae with sticky trichomes; E, the resulting three eggs surrounded by a foamy substance; F, immature collecting sticky substance from Melastomataceae with sticky trichomes.	Figure 2. Predatory and oviposition behaviours in Apiomerus flaviventris from California, USA (A–C), and in Heniartes spp. from Trinidad (D, E) and French Guiana (F): A, bee assassin with honey bee; B, female with resin-coated abdominal venter; C, resin transfer from abdominal storage area to eggs; D, female depositing eggs on Melastomataceae with sticky trichomes; E, the resulting three eggs surrounded by a foamy substance; F, immature collecting sticky substance from Melastomataceae with sticky trichomes.	2016-07-10	Forero, Dimitri;Weirauch, Christiane		Zenodo	biologists	Forero, Dimitri;Weirauch, Christiane			
0387774D3A769C6DFEB2FB16FECAFEAF.taxon	http://purl.org/dc/dcmitype/StillImage	image/png	https://zenodo.org/record/14806408/files/figure.png	https://doi.org/10.5281/zenodo.14806408	Figure 5. Ancestral state reconstruction of characters involved in resin storing and egg coating, and thus potentially indicative of maternal care behaviour. Female abdominal sternite setation (characters 111 and 110) suggests that resin storing may have evolved at the base of the Apiomerus + Manicococoris clades. Using the strongly sexually dimorphic metatibial comb as a proxy (character 35), used during egg coating, maternal care would be restricted to the Apiomerus clade.	Figure 5. Ancestral state reconstruction of characters involved in resin storing and egg coating, and thus potentially indicative of maternal care behaviour. Female abdominal sternite setation (characters 111 and 110) suggests that resin storing may have evolved at the base of the Apiomerus + Manicococoris clades. Using the strongly sexually dimorphic metatibial comb as a proxy (character 35), used during egg coating, maternal care would be restricted to the Apiomerus clade.	2016-07-10	Forero, Dimitri;Weirauch, Christiane		Zenodo	biologists	Forero, Dimitri;Weirauch, Christiane			
