| human | Q5 |
| P496 | ORCID iD | 0000-0002-3038-7424 |
| P1053 | ResearcherID | I-3707-2015 |
| P735 | given name | José | Q2190619 |
| José | Q2190619 | ||
| P6104 | maintained by WikiProject | WikiProject Invasion Biology | Q56241615 |
| P106 | occupation | researcher | Q1650915 |
| P21 | sex or gender | male | Q6581097 |
| Q42033058 | A 4 year follow-up analysis of genotoxic damage in birds of the Doñana area (south west Spain) in the wake of the 1998 mining waste spill |
| Q60234426 | A complex plumage pattern as an honest social signal |
| Q56937191 | A prioritised list of invasive alien species to assist the effective implementation of EU legislation |
| Q94922887 | A protective nesting association with native species counteracts biotic resistance for the spread of an invasive parakeet from urban into rural habitats |
| Q60393663 | A receiver bias for red predates the convergent evolution of red color in widowbirds and bishops |
| Q54899302 | An island paradigm on the mainland: host population fragmentation impairs the community of avian pathogens |
| Q54390805 | An island paradigm on the mainland: host population fragmentation impairs the community of avian pathogens. |
| Q48094375 | An overlooked plant-parakeet mutualism counteracts human overharvesting on an endangered tree |
| Q112494438 | Annual Censuses and Citizen Science Data Show Rapid Population Increases and Range Expansion of Invasive Rose-Ringed and Monk Parakeets in Seville, Spain |
| Q125875615 | Anthropogenic nesting sites and density of Burrowing Parrot (Cyanoliseus patagonus) in northern Argentinian Patagonia |
| Q60323906 | Apparent Absence of Blood Parasites in the Patagonian Seabird Community: Is It Related to the Marine Environment? |
| Q111845283 | Apparent Lack of Circovirus Transmission from Invasive Parakeets to Native Birds |
| Q111160278 | Assessing the introduction of exotic raptors into the wild from falconry |
| Q93012913 | Author Correction: Personality-dependent breeding dispersal in rural but not urban burrowing owls |
| Q128236109 | Bio-logging shows a central trans-Saharan migration and unknown wintering grounds in Africa of a juvenile griffon vulture from Spain |
| Q34716114 | Can synchronizing feather-based measures of corticosterone and stable isotopes help us better understand habitat-physiology relationships? |
| Q111147755 | Cities favour the recent establishment and current spread of the Eurasian collared dove Streptopelia decaocto (Frivaldszky, 1838) in Dominican Republic |
| Q55260367 | Cities may save some threatened species but not their ecological functions. |
| Q113799028 | Climate matching and anthropogenic factors contribute to the colonization and extinction of local populations during avian invasions |
| Q46324553 | Climate matching drives spread rate but not establishment success in recent unintentional bird introductions. |
| Q47374468 | Colony size selection determines adult survival and dispersal preferences: allee effects in a colonial bird |
| Q110626021 | Combined impacts of multiple non-native mammals on two life stages of a critically endangered Neotropical tree |
| Q56402072 | Combining trade data and niche modelling improves predictions of the origin and distribution of non-native European populations of a globally invasive species |
| Q110791015 | Components of breeding performance in two competing species: habitat heterogeneity, individual quality and density-dependence |
| Q60298536 | Conflicts between Lesser Kestrel Conservation and European Agricultural Policies as Identif ied by Habitat Use Analyses |
| Q46470238 | Correction: Truncated Power Laws Reveal a Link between Low-Level Behavioral Processes and Grouping Patterns in a Colonial Bird. |
| Q90965199 | Corticosterone implants produce stress-hyporesponsive birds |
| Q33779729 | Crowding in the city: losing and winning competitors of an invasive bird |
| Q57579425 | Current status of the threatened Dupont's lark Chersophilus duponti in Spain: overestimation, decline, and extinction of local populations |
| Q57579437 | DISPERSAL AND SOCIAL ATTRACTION AFFECT COLONY SELECTION AND DYNAMICS OF LESSER KESTRELS |
| Q56552073 | Dealing with non-native species: what makes the difference in South America? |
| Q57579374 | Describing dispersal under habitat constraints: A randomization approach in lesser kestrels |
| Q60323875 | Determining Sex of Magellanic Penguins Using Molecular Procedures and Discriminant Functions |
| Q31056696 | Developmental exposure to a toxic spill compromises long-term reproductive performance in a wild, long-lived bird: the white stork (Ciconia ciconia). |
| Q60298238 | Differences in acute stress responses between wild-caught and captive-bred birds: a physiological mechanism contributing to current avian invasions? |
| Q97525729 | Differences in adrenocortical responses between urban and rural burrowing owls: poorly-known underlying mechanisms and their implications for conservation |
| Q57579449 | Dispersal within a spatially structured population of lesser kestrels: the role of spatial isolation and conspecific attraction |
| Q42016911 | Disrupted bone metabolism in contaminant-exposed white storks (Ciconia ciconia) in southwestern Spain. |
| Q57579440 | Distress calls may honestly signal bird quality to predators |
| Q57579412 | Distress calls reflect poxvirus infection in lesser short-toed lark Calandrella rufescens |
| Q106606436 | Distribution of alien tetrapods in the Iberian Peninsula |
| Q57579427 | Does land irrigation actually reduce foraging habitat for breeding lesser kestrels? The role of crop types |
| Q57579324 | Don’t neglect pre-establishment individual selection in deliberate introductions |
| Q111321542 | Drivers of alien species composition in bird markets across the world |
| Q111159988 | Drivers of compositional dissimilarity for native and alien birds: the relative roles of human activity and environmental suitability |
| Q128236132 | Drivers of the Ectoparasite Community and Co-Infection Patterns in Rural and Urban Burrowing Owls |
| Q60298256 | Effects of habitat degradation on the abundance, richness and diversity of raptors across Neotropical biomes |
| Q57579442 | Effects of land use, nesting-site availability, and the presence of larger raptors on the abundance of Vulnerable lesser kestrels Falco naumanni in Kazakhstan |
| Q37193119 | Endangered plant-parrot mutualisms: seed tolerance to predation makes parrots pervasive dispersers of the Parana pine |
| Q111149439 | Epizoochory in Parrots as an Overlooked Yet Widespread Plant–Animal Mutualism |
| Q94497085 | Evaluation of genotoxic effects of heavy metals and arsenic in wild nestling white storks (Ciconia ciconia) and black kites (Milvus migrans) from southwestern Spain after a mining accident |
| Q54942029 | Evolution of genomic variation in the burrowing owl in response to recent colonization of urban areas. |
| Q96617364 | Experimental removal of invasive Africanized honey bees increased breeding population size of the endangered Lear's macaw |
| Q55711844 | Expression of concern. An island paradigm on the mainland: host population fragmentation impairs the community of avian pathogens. |
| Q47868076 | Extensive polymorphism and geographical variation at a positively selected MHC class II B gene of the lesser kestrel (Falco naumanni). |
| Q57579464 | Factors affecting breeding dispersal in the facultatively colonial lesser kestrel: individual experience vs. conspecific cues |
| Q56963697 | Feather mites (Acari: Astigmata) and body condition of their avian hosts: a large correlative study |
| Q60323914 | Feather mites on birds: costs of parasitism or conditional outcomes? |
| Q112068378 | Fine-scale genetic structure in the critically endangered red-fronted macaw in the absence of geographic and ecological barriers |
| Q51704576 | Fractal bird nest distribution produces scale-free colony sizes. |
| Q92075527 | Genes acting in synapses and neuron projections are early targets of selection during urban colonization |
| Q46522648 | Goats, birds, and emergent diseases: apparent and hidden effects of exotic species in an island environment |
| Q60298259 | Habitat, human pressure, and social behavior: Partialling out factors affecting large-scale territory extinction in an endangered vulture |
| Q36097102 | Heritability of fear of humans in urban and rural populations of a bird species |
| Q111154150 | High Prevalence of Novel Beak and Feather Disease Virus in Sympatric Invasive Parakeets Introduced to Spain From Asia and South America |
| Q30716840 | High individual consistency in fear of humans throughout the adult lifespan of rural and urban burrowing owls |
| Q35116319 | High urban breeding densities do not disrupt genetic monogamy in a bird species |
| Q92651736 | How much does it cost to save a species from extinction? Costs and rewards of conserving the Lear's macaw |
| Q34199376 | Illegal and legal parrot trade shows a long-term, cross-cultural preference for the most attractive species increasing their risk of extinction |
| Q33831530 | Individual consistency in flight initiation distances in burrowing owls: a new hypothesis on disturbance-induced habitat selection. |
| Q33883697 | Inter-individual variability in fear of humans and relative brain size of the species are related to contemporary urban invasion in birds. |
| Q35939273 | Internal seed dispersal by parrots: an overview of a neglected mutualism |
| Q60298244 | Is assisted colonization feasible? Lessons from past introductions |
| Q74170249 | Is cell-mediated immunity related to the evolution of life-history strategies in birds? |
| Q99603014 | Isolation and characterization of 15 new microsatellite markers for the globally endangered Lear's macaw Anodorhynchus leari |
| Q30438606 | Joint effects of population size and isolation on genetic erosion in fragmented populations: finding fragmentation thresholds for management |
| Q30817556 | Landscape bioacoustics allow detection of the effects of habitat patchiness on population structure. |
| Q60475579 | Large-scale impacts of multiple co-occurring invaders on monkey puzzle forest regeneration, native seed predators and their ecological interactions |
| Q39742267 | Lifetime fitness correlates of natal dispersal distance in a colonial bird |
| Q36035202 | Links between fear of humans, stress and survival support a non-random distribution of birds among urban and rural habitats |
| Q57579294 | Morphological variation in the specialist Dupont’s Lark Chersophilus duponti: geographical clines vs. local ecological determinants |
| Q113152503 | Multiple External Seed Dispersers Challenge the Megafaunal Syndrome Anachronism and the Surrogate Ecological Function of Livestock |
| Q55176539 | Nest-site competition and killing by invasive parakeets cause the decline of a threatened bat population. |
| Q89126705 | Network structure embracing mutualism-antagonism continuums increases community robustness |
| Q60234447 | Non-adaptive adoptions of nestlings in the colonial lesser kestrel: proximate causes and fitness consequences |
| Q56417570 | Non-random patterns and temporal trends (1912-2012) in the transport, introduction and establishment of exotic birds in Spain and Portugal |
| Q112768233 | Overlooked Parrot Seed Dispersal in Australia and South America: Insights on the Evolution of Dispersal Syndromes and Seed Size in Araucaria Trees |
| Q36418963 | Parasite prevalence and sample size: misconceptions and solutions. |
| Q36106913 | Parrots as key multilinkers in ecosystem structure and functioning |
| Q64098285 | Personality-dependent breeding dispersal in rural but not urban burrowing owls |
| Q38981696 | Predation of experimental nests is linked to local population dynamics in a fragmented bird population |
| Q57579434 | Proximate causes and fitness consequences of hatching failure in lesser kestrelsFalco naumanni |
| Q43580886 | RETRACTED: MHC diversity and differential exposure to pathogens in kestrels (Aves: Falconidae). |
| Q35868664 | Rapid loss of antipredatory behaviour in captive-bred birds is linked to current avian invasions |
| Q128236136 | Recent Advances in Parrot Research and Conservation |
| Q58427984 | Regional Bans on Wild-Bird Trade Modify Invasion Risks at a Global Scale |
| Q83183728 | Relationships between T-cell-mediated immune response and Pb, Zn, Cu, Cd, and as concentrations in blood of nestling white storks (Ciconia ciconia) and black kites (Milvus migrans) from Doñana (southwestern Spain) after the Aznalcóllar toxic spill |
| Q104281812 | Renewables in Spain threaten biodiversity |
| Q34172535 | Repeatability of feather mite prevalence and intensity in passerine birds |
| Q90003035 | Rethinking megafauna |
| Q57579460 | SOCIAL AND INDIVIDUAL FEATURES AFFECTING NATAL DISPERSAL IN THE COLONIAL LESSER KESTREL |
| Q41287691 | Seed dispersal by macaws shapes the landscape of an Amazonian ecosystem. |
| Q89679250 | Sex, personality and conspecific density influence natal dispersal with lifetime fitness consequences in urban and rural burrowing owls |
| Q36246033 | Sex- and age-dependent patterns of survival and breeding success in a long-lived endangered avian scavenger |
| Q35601219 | Shared genetic diversity across the global invasive range of the monk parakeet suggests a common restricted geographic origin and the possibility of convergent selection |
| Q28755374 | Song diversity predicts the viability of fragmented bird populations |
| Q57579359 | Strong philopatry derived from capture-recapture records does not lead to fine-scale genetic differentiation in lesser kestrels |
| Q111173211 | Successful hybridization between non‐congeneric parrots in a small introduced population |
| Q56144599 | Survival in a long-lived territorial migrant: effects of life-history traits and ecological conditions in wintering and breeding areas |
| Q60452514 | Survival in a long-lived territorial migrant: effects of life-history traits and ecological conditions in wintering and breeding areas |
| Q57579415 | Testing acoustic versus physical marking: two complementary methods for individual-based monitoring of elusive species |
| Q110626270 | The European trade ban on wild birds reduced invasion risks |
| Q33372336 | The PHA test reflects acquired T-cell mediated immunocompetence in birds |
| Q110626045 | The Role of Monk Parakeets as Nest-Site Facilitators in Their Native and Invaded Areas |
| Q60393492 | The authors reply |
| Q56425555 | The empty temporal niche: breeding phenology differs between coexisting native and invasive birds |
| Q90929692 | The extent, frequency and ecological functions of food wasting by parrots |
| Q33546065 | The paradox of the long-term positive effects of a North American crayfish on a European community of predators. |
| Q57579348 | The relative importance of patch habitat quality and landscape attributes on a declining steppe-bird metapopulation |
| Q33343587 | The role of despotism and heritability in determining settlement patterns in the colonial lesser kestrel |
| Q48166875 | The southernmost parakeet might be enhancing pollination of a dioecious conifer. |
| Q111160569 | Trends in legal and illegal trade of wild birds: a global assessment based on expert knowledge |
| Q33330282 | Truncated power laws reveal a link between low-level behavioral processes and grouping patterns in a colonial bird |
| Q60608687 | Uncoupled Evolution of Male and Female Cone Sizes in an Ancient Conifer Lineage |
| Q33799138 | Urban conservation hotspots: predation release allows the grassland-specialist burrowing owl to perform better in the city |
| Q57579404 | Who are we sampling? Apparent survival differs between methods in a secretive species |
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