La dimensión democrática de la nueva gestión pública

El eje temático de este nuevo número de la revista GAPP ha estado injustamente marginado de los apasionados debates que ha suscitado la modernización de la administración pública. La atracción que ha ejercido la gestión empresarial, las modas privatizadoras y desreguladoras o, más genéricamente, el desprestigio del gobierno y de la cosa pública contribuyen a explicar por qué, durante la última década, la dimensión democrática de la administración pública ha aparecido únicamente en algunas eruditas notas a pie de página. Esta marginación, sin embargo, no ha conseguido reducir la importancia del tema. Ha conseguido, en cambio, distorsionar peligrosamente el discurso de la modernización administrativa

The Rediscovery of a Long Described Species Reveals Additional Complexity in Speciation Patterns of Poeciliid Fishes in Sulfide Springs

The process of ecological speciation drives the evolution of locally adapted and reproductively isolated populations in response to divergent natural selection. In Southern Mexico, several lineages of the freshwater fish species of the genus Poecilia have independently colonized toxic, hydrogen sulfide-rich springs. Even though ecological speciation processes are increasingly well understood in this system, aligning the taxonomy of these fish with evolutionary processes has lagged behind. While some sulfide spring populations are classified as ecotypes of Poecilia mexicana, others, like P. sulphuraria, have been described as highly endemic species. Our study particularly focused on elucidating the taxonomy of the long described sulfide spring endemic, Poecilia thermalis Steindachner 1863, and investigates if similar evolutionary patterns of phenotypic trait divergence and reproductive isolation are present as observed in other sulfidic species of Poecilia. We applied a geometric morphometric approach to assess body shape similarity to other sulfidic and non-sulfidic fish of the genus Poecilia. We also conducted phylogenetic and population genetic analyses to establish the phylogenetic relationships of P. thermalis and used a population genetic approach to determine levels of gene flow among Poecilia from sulfidic and non-sulfidic sites. Our results indicate that P. thermalis' body shape has evolved in convergence with other sulfide spring populations in the genus. Phylogenetic analyses placed P. thermalis as most closely related to one population of P. sulphuraria, and population genetic analyses demonstrated that P. thermalis is genetically isolated from both P. mexicana ecotypes and P. sulphuraria. Based on these findings, we make taxonomic recommendations for P. thermalis. Overall, our study verifies the role of hydrogen sulfide as a main factor shaping convergent, phenotypic evolution and the emergence of reproductive isolation between Poecilia populations residing in adjacent sulfidic and non-sulfidic environments

Wallaceochromis gen. nov, a new chromidotilapiine cichlid genus (Pisces: Perciformes) from West Africa

Lamboj, Anton, Trummer, Franziska, Metscher, Brian D. (2016): Wallaceochromis gen. nov, a new chromidotilapiine cichlid genus (Pisces: Perciformes) from West Africa. Zootaxa 4144 (1): 124-130, DOI: http://doi.org/10.11646/zootaxa.4144.1.

Danakilia dinicolai Stiassny, Marchi & Lamboj, 2010, new species

Danakilia dinicolai, new species Figs. 2–4; Table 2 Holotype. MSNM 4888, male, 96.4 mm SL, Eritrea: Lake Abaeded. 14 ˚ 35 ' 17 " N, 40 ˚ 05' 04" E., G. De Marchi, January 1998. Paratypes. MSNM 4889, male, 72.9 mm SL, same data as holotype. MSNM 4890, female, 63.9 mm SL, same data as holotype. MSNM 4891, male, 56.7 mm SL, same data as holotype. AMNH 248881, 5 ex., 3 males, 2 females, 69.9–82.9 mm SL, Eritrea: Lake Abaeded, G. De Marchi, March 2001. AMNH 251633 4 ex. (1 C&S), 1 male, 3 females, 63.6–76.5 mm SL, Eritrea: Lake Abaeded, G. De Marchi, March 2001. MSNG 55210, 1 female, 73.0 mm SL, Eritrea: Lake Abaeded. 14 ˚ 35 ' 17 " N, 40 ˚ 05' 04", E., G. De Marchi, March 2001. Diagnosis. Differs from its only congener, Danakilia franchettii, in the possession of longer pectoral fins (31.1–38.7 % SL vs. 21.7–30.6 % SL). Outer row teeth in both oral jaws composed of stout tricuspids, considerably more robust and fewer in number than those of D. franchettii. Lower pharyngeal bone relatively massive, longer than wide, length 30–32 % HL (vs. small, only slightly longer than wide, length 25–27 % HL in D. franchettii), with 40–48 teeth in posterior row (vs. 26–36 in D. franchettii). Description. Based on holotype and 13 paratypes. Maximum size 96.4 mm SL. Counts and proportional measurements are given in Table 2. Snout acute, mouth terminal, lips thickened but not fleshy. Head large, snout conical with straight profile, head smoothly convex behind nape to dorsal fin, except in largest males with a bulbous frontal gibbosity, particularly evident in life (Figs. 2 & 4 B). Greatest body depth between insertion of dorsal and pelvic fins. Caudal peduncle always longer than deep. Caudal fin truncate. Dorsal XIII–XIV 9–11. Anal III 7 or 8. Pectoral fin long, reaching to anal fin origin or beyond. First pelvic ray longer in males than females but pelvic fin always reaching anus, and often beyond anal origin. Jaws isognathous, both with 2–4 rows of tricuspid teeth. Outer row teeth in both jaws stout tricuspids with small, symmetrically rounded lateral cusps and larger medial cusp (Fig. 3 A), considerably more robust and fewer in number than in D. franchettii (Fig. 3 B). Lower pharyngeal bone relatively massive, longer than wide (Fig. 3 A), length 30–32 % HL (versus small, only slightly longer than wide, length 25–27 % HL in D. franchettii (Fig. 3 B). Pharyngeal teeth in anterior field of jaw, robust unicuspids, sparsely implanted, becoming increasingly elongate, recurved and spatulate posteriorly, densely implanted over posterior field of jaw, 40–48 teeth in posterior row (Fig. 3 A). Pharyngeal teeth in D. franchettii are similarly arrayed, but coarser and less densely implanted in posterior field of jaw, 26–36 teeth in posterior row (Fig. 3 B). Eleven to 14 small, moderately tuberculate gill rakers along lower limb of first arch (including raker at angle), 2 or 3 pointed epibranchial rakers. Microbranchiospines absent. Scales cycloid, 2 or 3 rows on cheek, 2–4 horizontal rows on opercle. Dark scaleless spot on outer edge of opercle. Chest and belly scales deeply embedded, markedly smaller than on flank, 4 or 5 scales between pectoral and pelvic fins. Upper lateral line separated from dorsal fin anteriorly by 3 or 4 scale rows, at 8 th pored scale by 2 scale rows, at last pored scale by 1–1.5 scale rows. End of upper lateral line separated from lower lateral line by 1 or 2 scale rows. Basal 1 / 3 of caudal fin covered with scales; other fins unscaled. holotype mean SD Range Standard length 96.4 77.9 63.6–96.4 Caudal peduncle length % as of depth 120.2 118.7 8.3 102.8–128.8 median Gill rakers on lower limb of first arch 12 12 11–14 Total gill rakers on first arch 14 14 13–17 Miscellaneous osteology. Infraorbital series complete, with lachrymal (first infraorbital) and four tubular infraorbitals, lachrymal with five openings of laterosensory system. Total of 25 or 26 vertebrae, 11–13 precaudal and 12–14 caudal. Inferior vertebral apophysis (spondylophysial apophysis) supporting anterior end of gas bladder composed of elongate ventro-posteriorly directed process on 3 rd vertebral centrum which abuts a stout ventro-posteriorly directed process on 4 th centrum; similar in form and composition to that of Iranocichla (Fig. 3 D). Coloration in life. Females and non-dominant males (Fig. 4 A). Opercule and body pale silvery-grey, snout and nape dark brownish-black. Dark scaleless spot on outer edge of opercle variously intense, but always present. Upper lip with bluish cast, lower lip grey. Throat and branchiostegal membranes pale silvergrey. Two dark longitudinal stripes sometimes visible on flanks, upper stripe at level of upper lateral line, passing to end of dorsal-fin base, lower stripe from edge of opercle to caudal base, not extending into caudal fin. Sometimes 5–7 dark vertical bars on body from dorsal-fin base to ventrum. Eye golden-yellow to brownish-black. Dominant males (Fig. 4 B). Dorsal, caudal and anal fins pale blue, with numerous paler blue dots. White margin of dorsal fin flushed pale red-orange distally. Thin white margin on upper caudal lobe. Pelvics blue, paler distally. Body scales with iridescent, pale blue posterior margins, centrally grey to greyishblack. Scales on chest and belly silvery grey, with darker grey margins. Prominent frontal gibbosity blackishblue to greyish-blue. Snout and lips pale blue. Coloration in preservation (Fig. 2). Both sexes with head and body brown, darker dorsally, with dark lines or bars often visible as described in living specimens. Dorsal, anal and caudal fins heavily spotted in males, less so in females. Feeding behaviour. No field observations made, but gut morphology and contents suggests a diet primarily consisting of algae grazed from the surface of plants and rocks. Guts are highly coiled, and extend to 7.6 times SL, most are filled with floculent algae with some sand grains and vegetable debris. However, it is likely that this species is an opportunistic feeder, as individuals were caught on lines baited with grasshoppers. Breeding behaviour. Unknown, but large males guarding pits over sand were observed in the field. Distribution and habitat (Fig. 5). Lake Abaeded occupies a small oval depression (maximum width of 450 m, maximum depth 10 m) in a volcanic crater at the northwestern border of the Danakil Depression in Eritrea, 132 km southeast of the coastal town of Massawa. Lake surface is about 30 m below sea level. Sand from dunes along the eastern and southern rim is frequently blown into the lake. The lake is fed by many hot springs at surface level and underwater, and as there is no surface outlet evaporation in this hyper arid region (rainfall of ~ 5 m /year) probably fully compensates for the input from springs to maintain a stable lake level year round. In April 1998 water temperature was 29 °C but reached 45 °C close to the hot springs. Total salinity was 14.5 gr/l. The most abundant ions were Na+ (111 EPM), Ca++ (99 EPM), Mg++ (18 EPM), Cl - (217 EPM) and SO 4 - (41 EPM). Ph was 7.46 and EC was 23100. High concentrations of Na+, Ca++, Cl - and SO 4 - are certainly the result of circulation of water heated at depth through layers of gypsum and halite that cover the bottom of the northern part of the Danakil Depression (Gasse & Street 1978). The lakeshore is almost completely encircled by reeds (Phragmites australis) and stands of tamarisk (Tamarix aphylla), but is free of vegetation in the proximity of hot springs. A single non-piscine vertebrate inhabiting the lake is a frog, probably Ptychadena anchietae. Fishes are abundant in the lake and concentrate among the reeds, but are found also on sandy substrate near the shore, where temperature is not too high. The bottom of the sandy areas is covered with crater-like nests dug and defended by large colourful males. The species has been found so far only in Lake Abaeded, but no research has yet been conducted in the nearby Lake Badda, a variable surface reed-fringed lake only 8 km north of Lake Abaeded (Fig. 5). Etymology. Named in memory of Ernesto Di Nicola, a member of the 2001 expedition to Lake Abaeded who died in a car accident while returning from the lake. Discussion. The discovery of a second species of Danakilia in a small lake currently isolated by some 160 km of hyper-arid desert from its congener, Danakilia franchettii, raises the question of the age and origin of these two isolated species. The geological history of the region indicates that the Danakil Depression formed as a result of tectonic movements related to the Afro-Arabian Rift (Beyene & Abdelsalam 2005). It was an intermittent marine basin (at least in the northern region) during the late Pleistocene, and with the formation of volcanic structures at the northern end it is thought to have separated from the Red Sea sometime around 32,000 – 25,000 years ago (Bonatti 1971, Barberi et al. 1972). Separation of the two species of Danakilia might therefore date back to the Pleistocene to the time of the formation of the Alayta e Tat'Ale shield volcanoes that surround Lake Afdera (Barberi et al. 1972). Alternatively, their separation may be considerably younger having occurred after the drying of extensive saline lakes that occupied the bottom of the Danakil Depression during a major arid phase that started about 9,000 – 5,000 years ago (Gasse 1974, Gasse & Street 1978). Unfortunately, despite considerable effort all attempts to extract DNA from either species have so far failed, and molecular divergence time estimates cannot be made until additional material becomes available.Published as part of Stiassny, Melanie L. J., Marchi, Giuseppe De & Lamboj, Anton, 2010, A new species of Danakilia (Teleostei, Cichlidae) from Lake Abaeded in the Danakil Depression of Eritrea (East Africa), pp. 43-52 in Zootaxa 2690 on pages 45-51, DOI: 10.5281/zenodo.19952

Data from: The rediscovery of a long described species reveals additional complexity in speciation patterns of poeciliid fishes in sulfide springs

The process of ecological speciation drives the evolution of locally adapted and reproductively isolated populations in response to divergent natural selection. In Southern Mexico, several lineages of the freshwater fish species of the genus Poecilia have independently colonized toxic, hydrogen sulfide-rich springs. Even though ecological speciation processes are increasingly well understood in this system, aligning the taxonomy of these fish with evolutionary processes has lagged behind. While some sulfide spring populations are classified as ecotypes of Poecilia mexicana, others, like P. sulphuraria, have been described as highly endemic species. Our study particularly focused on elucidating the taxonomy of the long described sulfide spring endemic, Poecilia thermalis Steindachner 1863, and investigates if similar evolutionary patterns of phenotypic trait divergence and reproductive isolation are present as observed in other sulfidic species of Poecilia. We applied a geometric morphometric approach to assess body shape similarity to other sulfidic and non-sulfidic fish of the genus Poecilia. We also conducted phylogenetic and population genetic analyses to establish the phylogenetic relationships of P. thermalis and used a population genetic approach to determine levels of gene flow among Poecilia from sulfidic and non-sulfidic sites. Our results indicate that P. thermalis' body shape has evolved in convergence with other sulfide spring populations in the genus. Phylogenetic analyses placed P. thermalis as most closely related to one population of P. sulphuraria, and population genetic analyses demonstrated that P. thermalis is genetically isolated from both P. mexicana ecotypes and P. sulphuraria. Based on these findings, we make taxonomic recommendations for P. thermalis. Overall, our study verifies the role of hydrogen sulfide as a main factor shaping convergent, phenotypic evolution and the emergence of reproductive isolation between Poecilia populations residing in adjacent sulfidic and non-sulfidic environments

Body shape data for the dorsal projection

The file contains the aligned landmark coordinates for body shape in the dorsal projection. For each individual, we also provide information on the species designation, collection location, drainage, whether the habitat is sulfidic or not, sex, and centroid size

Body shape data for the lateral projection

The file contains the aligned landmark coordinates for body shape in the lateral projection. For each individual, we also provide information on the species designation, collection location, drainage, whether the habitat is sulfidic or not, sex, and centroid size

Microsatellite data

The excel files contains all raw data from population genetic analyses as described in the paper. Specimens are grouped by collection site (as per Table 2 in the main manuscript). Microsatellite loci are grouped by multiplex reactions. Locus names follow Slattery et al. (2012): Twelve new microsatellite loci for the sulphur molly (Poecilia sulphuraria) and the related Atlantic molly (P. mexicana). Conservation Genetics Resources 4 (4): 935-937

Hierarchical cluster analysis of <i>Poecilia</i> populations from sulfidic and non-sulfidic environments based on body shape variation in the lateral and dorsal projections.

<p>Colors denote sulfide-adapted (yellow) and non-adapted (blue) populations of three species, <i>Poecilia thermalis</i> (yellow circles), <i>P. sulphuraria</i> (yellow triangles), and <i>P. mexicana</i>. The shapes represent the drainages (diamonds- Tacotalpa, squares- Puyacatengo, circles- Ixtapangajoya, and triangles- Pichucalco) and the numbers correspond to sites as described in <a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0071069#pone-0071069-t002" target="_blank">Table 2</a>.</p