taxonID	type	description	language	source
5425879D3E408D56FF02F93207B94E97.taxon	description	(Fig. 2) Material examined. 1 ind. (CZ-UFRPE 18010), Camucim Forest Protected Area, São Lourenço da Mata, Pernambuco, 8 ° 02 ’ 18.2 ’’ S 35 ° 12 ’ 2.97 ’’ W (WGS 84), 09 May 2018, colls. R. F. de Oliveira and F. A. Santos; 7 ind. (CZ-UFRPE 18011), 4 ind. (CZ-UFRPE 18029), Camucim Forest Protected Area, São Lourenço da Mata, Pernambuco, 8 ° 02 ’ 14 ’’ S 35 ° 12 ’ 01 ’’ W, 09 – 10 May 2018, colls. R. F. de Oliveira and F. A. Santos; 1 ind. (CZ-UFRPE 18019), Camucim Forest Protected Area, São Lourenço da Mata, Pernambuco, 8 ° 01 ’ 59.8 ” S 35 ° 12 ’ 03.8 ” W, 10 May 2018, colls. R. F. de Oliveira and F. A. Santos. Specimens. All M. dumonti specimens have morphological characters corresponding to the original description (Kotov et al., 2005) (Fig. 2); with body structures of parthenogenetic females (Fig. 2 a) and males (Fig. 2 b), although it was not possible to observe the presence of ocellae at the base of the first antenna. Females show short and practically cylindrical antennae, with an aesthetasc tip of similar size (Fig. 2 c); whereas males showed long and slightly curved antennae, distally with four similar hook-like setae (Fig. 2 d). Postabdomen with terminal claw showing basal pecten with five spines in females (Fig. 2 e) and four in males (Fig. 2 f). All males showed the same set of spines on the basal pecten. This morphological character easily distinguishes this species from its congeners. The setulated hook in the dorsal portion of the posterior valve observed by Farias et al. (2017) does not exist in females (Fig. 2 g) or males (Fig. 2 h) sampled in the present study. Ecology and habitat. Parthenogenetic females, ephippials and males were collected in two distinct environments: two ponds with riparian vegetation and a predominance of the macrophyte Lemna on the waterline; and one pond without riparian vegetation and a predominance of the macrophyte Azolla. These environments showed population densities of 27,208 ind / m ³ and 833 ind / m ³, respectively. The influence of riparian vegetation on the zooplanktonic communities of these ponds was described by Medeiros et al. (2019), who associated the occurrence of M. dumonti with low water turbidity (45.81 ± 27.84 NTU), high oxygenation (5.17 ± 2.10 mg L- 1), and variable a- chlorophyll concentrations (23.31 ± 28.07 µg L- 1). Distribution. Since its description, M. dumonti has been recorded in three environments in the world: two temporary habitats in Mexico and Cuba (Kotov et al., 2005) and one perennial lagoon in Rio de Janeiro, Brazil (Farias et al., 2017). In this study, the specimens were recorded in a habitat similar to its type-locality, temporary ponds, for the first time in the Brazilian Northeast region (Fig. 1). Thus, this species is now recorded in Southeast Atlantic (SE) and Oriental Northeast Atlantic (NOr) hydrographic regions of Brazil.	en	Júnior, Íttalo Luã Silva Medeiros Felipe Antonio dos Santos Ralf Tarciso Silva Cordeiro Mauro de Melo (2021): New records of two cladoceran species (Branchiopoda: Anomopoda) from Northeastern Brazil: the importance of studies in temporary ponds. Nauplius (e 2021038) 29: 1-10, DOI: 10.1590/2358-2936e2021038, URL: https://doi.org/10.1590/2358-2936e2021038
5425879D3E468D56FED3F99903BC4C0D.taxon	description	(Fig. 3) Material examined. 1 ind. (CZ-UFRPE 18008), Camucim Forest Protected Area, São Lourenço da Mata, Pernambuco, 8 ° 02 ’ 24.8 ” S 35 ° 11 ’ 48.5 ” W (WGS 84), 09 May 2018, colls. R. F. de Oliveira and F. A. Santos; 12 ind. (CZ-UFRPE 18010), 2 ind. (CZ-UFRPE 18034), Camucim Forest Protected Area, São Lourenço da Mata, Pernambuco, 8 ° 02 ’ 18.2 ’’ S 35 ° 12 ’ 2.97 ’’ W (WGS 84), 09 and 11 May 2018, colls. R. F. de Oliveira and F. A. Santos. Specimens. The specimens of C. nitidulus show characters similar to their latest descriptions (Elmoor-Loureiro, 1997). In Fig. 3 a, the body structure of a parthenogenetic female is represented, with oval body and postabdomen exposed. Arrow indicates the naked and elongated labral keel, which is diagnostic for this species. Details of postabdomen are typical, showing terminal claw chitinized and curved, with two basal spines of different sizes (Fig. 3 b). Valves have one denticle in the posteroventral corner (Fig. 3 c). Ecology and habitat. Parthenogenetic females of C. nitidulus were recorded in environments limnologically distinct from those of M. dumonti, although both species were collected in stations dominated by Lemna. The specimens sampled in the present study occurred in ponds with both degraded and preserved riparian vegetation, which show high turbidity (132 ± 96.55 NTU), low oxygenation (3.57 ± 2.73 mg L- 1) and low a- chlorophyll concentration (14.24 ± 13.76 µg L- 1). Distribution. Chydorus nitidulus is a Neotropical species, previously recorded in Venezuela (Rey and Vásquez, 1886; Vásquez and Rey, 1989), Argentina (Paggi, 1972), Brazil (Elmoor-Loureiro, 1997), Mexico (Elías-Gutiérrez et al., 2006), and Colombia (Fuentes-Reinés, 2014; Fuentes-Reinés et al., 2019). In Brazil, this species was mainly recorded in the hydrographic regions of Amazonia (AM), Paraguay (PG), Paraná (PR), São Francisco (SF), East (AL), South (SA) and Southeast Atlantic (SE), and Tocantins / Araguaia (TA) (see Fig. 1 and Tab. 1, for references). Thus, this study expands the distribution of C. nitidulus to the Oriental Northeast Atlantic hydrographic region (NOr) and to Atlantic forest ponds in Northeastern Brazil.	en	Júnior, Íttalo Luã Silva Medeiros Felipe Antonio dos Santos Ralf Tarciso Silva Cordeiro Mauro de Melo (2021): New records of two cladoceran species (Branchiopoda: Anomopoda) from Northeastern Brazil: the importance of studies in temporary ponds. Nauplius (e 2021038) 29: 1-10, DOI: 10.1590/2358-2936e2021038, URL: https://doi.org/10.1590/2358-2936e2021038
