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  • 1
  • 2
    Publication Date: 2016-09-06
    Description: In North America, most species of the Candonidae family belong to the genus Candona. These species are frequently found in freshwater ecosystems and in sediment sequences, which makes them valuable tools for paleoenvironmental reconstructions. Knowledge of Mexican Candona species is limited, however, and scant information exists regarding their taxonomy and ecology. Here we describe Candona alchichica, a new ostracod species we suggest being endemic to Lake Alchichica, central Mexico. The species belongs to the acuminata group of species, based on the presence of 5+1 setae on the second segment of the mandibular palp. It is closely related to C. patzcuaro, C. tahoensis and C. ohioensis, but differs from those species in that the females have an elongated genital field, wide at the base and narrow at the end. Males have elongated hook-like prehensile palps and a particular arrangement of lobes in the hemipenis, i.e., the a-lobe is inclined with a digitiform basal projection, the b-lobe is distally rounded and the h-lobe is square-shaped and exceeding the length of the b-lobe. Candona alchichica n. sp. and C. patzcuaro display very similar shells in length and morphology, which can cause confusion if identification is carried out in the absence of soft parts, a common situation when dealing with carapace and valve remains in sediment cores. Detailed morphometric analyses, however, revealed a clear difference between the valves of the two taxa. Candona alchichica n. sp. has taller valves (p˂0.05), with concave dorsal margin, and with the anterior margin considerably narrower than posterior margin, all characteristics different from C. patzcuaro. Most important, in spite of their similar shape, the two species exhibit contrasting ecological preferences. Candona alchichica n. sp. inhabits clear, cold, saline, oligotrophic waters, whereas C. patzcuaro dwells in turbid, warm, fresh, eutrophic waters. In addition, we include a revision of the morphological characteristics and taxonomic position of C. patzcuaro, based on type material and specimens collected from the type locality (i.e., Lake Pátzcuaro, Michoacán). This study highlights the importance of undertaking detailed morphometric analyses of the recent ostracod fauna to provide reliable taxonomic identifications and ecological characterizations of species, which are critical for accurate paleoclimatic and paleoecological reconstructions.
    Print ISSN: 1129-5767
    Electronic ISSN: 1723-8633
    Topics: Biology
    Published by PAGEPress
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  • 3
    Publication Date: 2020-01-16
    Description: We evaluated how ranges of four endemic and non-endemic aquatic ostracode species changed in response to long-term (glacial–interglacial cycles) and abrupt climate fluctuations during the last 155 kyr in the northern Neotropical region. We employed two complementary approaches, fossil records and species distribution models (SDMs). Fossil assemblages were obtained from sediment cores PI-1, PI-2, PI-6 and Petén-Itzá 22-VIII-99 from the Petén Itzá Scientific Drilling Project, Lake Petén Itzá, Guatemala. To obtain a spatially resolved pattern of (past) species distribution, a downscaling cascade is employed. SDMs were reconstructed for the last interglacial (∼120 ka), the last glacial maximum (∼22 ka) and the middle Holocene (∼6 ka). During glacial and interglacial cycles and marine isotope stages (MISs), modelled paleo-distributions and paleo-records show the nearly continuous presence of endemic and non-endemic species in the region, suggesting negligible effects of long-term climate variations on aquatic niche stability. During periods of abrupt ecological disruption such as Heinrich Stadial 1 (HS1), endemic species were resilient, remaining within their current areas of distribution. Non-endemic species, however, proved to be more sensitive. Modelled paleo-distributions suggest that the geographic range of non-endemic species changed, moving southward into Central America. Due to the uncertainties involved in the downscaling from the global numerical to the highly resolved regional geospatial statistical modelling, results can be seen as a benchmark for future studies using similar approaches. Given relatively moderate temperature decreases in Lake Petén Itzá waters (∼5 ∘C) and the persistence of some aquatic ecosystems even during periods of severe drying in HS1, our data suggest (1) the existence of micro-refugia and/or (2) continuous interaction between central metapopulations and surrounding populations, enabling aquatic taxa to survive climate fluctuations in the northern Neotropical region.
    Print ISSN: 1726-4170
    Electronic ISSN: 1726-4189
    Topics: Biology , Geosciences
    Published by Copernicus on behalf of European Geosciences Union.
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  • 4
  • 5
    Publication Date: 2019-09-09
    Description: We evaluated how ranges of four endemic and non-endemic aquatic ostracode species changed in response to long-term (glacial-interglacial cycles) and abrupt climate fluctuations during the last 155 ka in the northern Neotropical region. We employed two complementary approaches, fossil records and species distribution modeling (SDM). Fossil assemblages were obtained from sediment cores PI-1, PI-2, PI-6 and Petén-Itzá 22-VIII-99 from Petén Itzá Scientific Drilling Project, Lake Petén Itzá, Guatemala. To obtain a spatially resolved pattern of (past) species distribution, a downscaling cascade is employed. SDM's were reconstructed for the Last Interglacial (~ 120 ka BP), the Last Glacial Maximum (~ 22 ka BP) and the middle Holocene (~ 6 ka BP). During glacial/interglacial cycles and Marine Isotope Stages, modeled paleo-distributions and paleo-records show nearly continuous presence of endemic and non-endemic species in the region, suggesting negligible effects of long-term climate variations on aquatic niche stability. During periods of abrupt ecological disruption such as Heinrich Stadial 1 (HS1), endemic species were resilient, remaining within their current areas of distribution. Non-endemic species, however, proved to be more sensitive. Modeled paleo-distributions suggest that the geographic range of non-endemic species changed, moving southward into Central America. Due to the uncertainties involved in the downscaling from the global numerical to the highly resolved regional geospatial statistical modelling, results can be seen as benchmark for future studies using similar approaches. Given relatively moderate temperature decreases in Lake Petén Itzá waters (~ 5 ºC) and persistence of some aquatic ecosystems even during periods of severe drying in HS1, our data suggest 1) existence of micro-refugia and/or 2) continuous interaction between central metapopulations and surrounding populations, enabling aquatic taxa to survive climate fluctuations in the northern Neotropical region.
    Print ISSN: 1810-6277
    Electronic ISSN: 1810-6285
    Topics: Biology , Geosciences
    Published by Copernicus on behalf of European Geosciences Union.
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  • 6
    Publication Date: 2021-02-08
    Description: Highlights • Evaluation of environmental variability induced by Heinrich Stadials (HS5a-HS1) in continental northern Neotropical region. • Multiproxy evidence reveals mild temperature decreases and drastic fluctuations in precipitation during HSs. • Ultrastructure of HSs suggests individual environmental response of each Stadial making them contrasting from each other. • Most drastic climate changes induced by HSs exerted positive effects on diversity of aquatic communities. Abstract We reconstruct environmental conditions of the period 53-14 kyr BP in the continental northern Neotropical region. We evaluate in detail the magnitude of climatic fluctuations and their effects on aquatic communities during six Heinrich Stadials (HS1-HS5a), using sediments from Lake Petén Itzá, Guatemala, and a multiproxy approach. In Lake Petén Itzá typical Heinrich Stadials (HSs) are recorded in sediments as alternations of gypsum and clay, and abrupt changes in magnetic susceptibility, CaCO3 and biological compositions. This suggests that HSs were periods of hydrological unbalance, characterized by dry spells, punctuating the predominant humid conditions characterizing the period 53-14 kyr BP. The ultrastructure of HSs allows us to identify four different types of climatic conditions associated to HSs: 1) prevailing dry conditions but changing to humid (HS5, HS3); 2) predominantly humid conditions but changing to arid (HS2); 3) fluctuating humid-dry-humid (HS4, HS1); and 4) arid with high lake water conductivity (HS5a). The continuous presence of tropical ostracode species during HSs suggests that lake water temperatures were not drastically lowered. Ostracode-based transfer functions indicate that during HSs, epilimnetic water temperatures decreased by 1–3 °C compared to mean modern temperatures. Lake solute composition and conductivity were strongly affected by HSs. During HS5a and HS1 we estimate conductivity values 〉 800 μS cm−1. Diversity indices show significant differences (F5,70 = 3.74, p = 0.004) of ostracode species composition among HSs. Highest diversities occurred during HS5a, HS4 and HS1, which display greater climatic alterations than the other HSs. Fluctuating climates seem to have exerted positive effects on diversity of aquatic communities by producing an increase in habitat heterogeneity.
    Type: Article , PeerReviewed
    Format: text
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  • 7
  • 8
    Publication Date: 2024-02-07
    Description: The last 85,000 years were characterized by high climate and environmental variability on the Yucatán Peninsula. Heinrich stadials are examples of abrupt climate transitions that involved shifts in regional temperatures and moisture availability. Thus, they serve as natural experiments to evaluate the contrasting responses of aquatic and terrestrial ecosystems. We used ostracodes and pollen preserved in a 75.9-m-long sediment core (PI-6, ~85 ka) recovered from Lake Petén Itzá, Guatemala, to assess the magnitude and velocity of community responses. Ostracodes are sensitive to changes in water temperature and conductivity. Vegetation responds to shifts in temperature and the ratio of evaporation to precipitation. Ostracodes display larger and more rapid community changes than does vegetation. Heinrich Stadial 5-1 (HS5-1) was cold and dry and is associated with lower ostracode and vegetation species richness and diversity. In contrast, the slightly warmer and dry conditions during HS6 and HS5a are reflected in higher ostracode species richness and diversity. Our paleoecological study revealed the greatest ecological turnover for ostracodes occurred from 62.5 to 51.0 ka; for pollen, it was at the Pleistocene/Holocene transition. Future studies should use various climate and environmental indicators from lake and marine sediment records to further explore late glacial paleoclimate causes and effects in the northern neotropics.
    Type: Article , PeerReviewed
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  • 9
    Publication Date: 2024-05-24
    Description: We evaluated how ranges of four endemic and non-endemic aquatic ostracode species changed in response to long-term (glacial–interglacial cycles) and abrupt climate fluctuations during the last 155 kyr in the northern Neotropical region. We employed two complementary approaches, fossil records and species distribution models (SDMs). Fossil assemblages were obtained from sediment cores PI-1, PI-2, PI-6 and Petén-Itzá 22-VIII-99 from the Petén Itzá Scientific Drilling Project, Lake Petén Itzá, Guatemala. To obtain a spatially resolved pattern of (past) species distribution, a downscaling cascade is employed. SDMs were reconstructed for the last interglacial (∼120 ka), the last glacial maximum (∼22 ka) and the middle Holocene (∼6 ka). During glacial and interglacial cycles and marine isotope stages (MISs), modelled paleo-distributions and paleo-records show the nearly continuous presence of endemic and non-endemic species in the region, suggesting negligible effects of long-term climate variations on aquatic niche stability. During periods of abrupt ecological disruption such as Heinrich Stadial 1 (HS1), endemic species were resilient, remaining within their current areas of distribution. Non-endemic species, however, proved to be more sensitive. Modelled paleo-distributions suggest that the geographic range of non-endemic species changed, moving southward into Central America. Due to the uncertainties involved in the downscaling from the global numerical to the highly resolved regional geospatial statistical modelling, results can be seen as a benchmark for future studies using similar approaches. Given relatively moderate temperature decreases in Lake Petén Itzá waters (∼5 ∘C) and the persistence of some aquatic ecosystems even during periods of severe drying in HS1, our data suggest (1) the existence of micro-refugia and/or (2) continuous interaction between central metapopulations and surrounding populations, enabling aquatic taxa to survive climate fluctuations in the northern Neotropical region.
    Type: Article , PeerReviewed
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  • 10
    Publication Date: 2023-03-14
    Description: Here, we present 23 water physical (temperature, dissolved oxygen, pH, conductivity) and chemical (major anions Cl-, SO42-, CO32-, HCO3- and cations Ca2+, K+, Mg2+, Na+), sedimentological (total carbon (TC), total inorganic carbon (TIC), total organic carbon (TOC), total nitrogen (TN)), mineralogical (quartz, carbonate, phyllosilicates and feldspars) and geological (altitude, bedrock type and age of sediments) variables of aquatic systems of the Northern Neotropical region. Sampling was conducted in 76 aquatic systems during July-October 2013, coinciding with the rainy season in the region. Sampling sites are located on the Yucatán Peninsula Mexico (n=28), Guatemala (n=26), El Salvador (n=14), Honduras (n=5) and Nicaragua (n=3). We aim to identify limnological regions based on the measured variables and to infer the influence of geodiversity in observed patterns. Water physical and chemical variables were measured in situ with a WTW Multi Set 350i multiparameter probe at a water depth of 0.5 m. Water samples for analysis of major anions and cations were collected at water depths of 0.5 m below surface. TC and TN in sediments contents were determined by combustion with a LECO TruSpec Macro CHN analyzer. TIC was quantified with a Woesthoff Carmhograph C-16. TOC was calculated by subtracting TIC from TC. Qualitative and semi-quantitative mineralogical compounds were examined by x-ray diffraction with a RIGAKU Miniflex600. ArcGIS software was used to identify geological attributes of sampling sites such as bedrock and age of sediments. Altitude, latitude, and longitude were determined with the navigator Garmin GPSmap 60c.
    Keywords: ArcGIS software; Bedrock type; Bicarbonate ion; Calcium; Calculated by subtracting TIC from TC; Carbon, inorganic, total; Carbon, organic, total; Carbon, total; Carbonate; Carbonate, Intensity; Chloride; Conductivity, electrolytic; DATE/TIME; DEPTH, water; Device type; ELEVATION; Epoch; Event label; Feldspar, Intensity; LATITUDE; LECO TruSpec Macro CHN analyzer; Limnolgy; LONGITUDE; Magnesium; mineralogy; MULT; Multiple investigations; Nitrogen, total; northern Neotropical region; northern Neotropics; Oxygen; pH; Phyllosilicates, Intensity; Potassium; Quartz, intensity; Sample ID; Sedimentology; Sodium; Sulfate; Temperature, water; Woesthoff Carmhograph C-16; WTW Multi Set 350i multiparameter probe; X-ray diffraction (RIGAKU Miniflex600); YP-GSHN-2013; YP-GSHN-2013_ALE; YP-GSHN-2013_AMA; YP-GSHN-2013_APA; YP-GSHN-2013_ARA; YP-GSHN-2013_ATI; YP-GSHN-2013_BAC; YP-GSHN-2013_CAL; YP-GSHN-2013_CAMP; YP-GSHN-2013_CAN; YP-GSHN-2013_CAO; YP-GSHN-2013_CH1; YP-GSHN-2013_CH2; YP-GSHN-2013_CHA; YP-GSHN-2013_CHI; YP-GSHN-2013_COA; YP-GSHN-2013_COL; YP-GSHN-2013_COM; YP-GSHN-2013_CSAB; YP-GSHN-2013_DIE; YP-GSHN-2013_EMI; YP-GSHN-2013_ENC; YP-GSHN-2013_ESP; YP-GSHN-2013_GLO; YP-GSHN-2013_GMI; YP-GSHN-2013_GRA; YP-GSHN-2013_GUI; YP-GSHN-2013_ILO; YP-GSHN-2013_IPA; YP-GSHN-2013_ITZ; YP-GSHN-2013_JOC; YP-GSHN-2013_JOS; YP-GSHN-2013_JUA; YP-GSHN-2013_JUC; YP-GSHN-2013_KAN; YP-GSHN-2013_LAC; YP-GSHN-2013_LCH1; YP-GSHN-2013_LCH2; YP-GSHN-2013_MAD; YP-GSHN-2013_MAG; YP-GSHN-2013_MAN; YP-GSHN-2013_MAS; YP-GSHN-2013_MET; YP-GSHN-2013_MIG; YP-GSHN-2013_MIS; YP-GSHN-2013_MU1; YP-GSHN-2013_MU2; YP-GSHN-2013_MUY; YP-GSHN-2013_NAG; YP-GSHN-2013_NEG; YP-GSHN-2013_NIC; YP-GSHN-2013_NOH; YP-GSHN-2013_OLO; YP-GSHN-2013_OQU; YP-GSHN-2013_OXO; YP-GSHN-2013_PE1; YP-GSHN-2013_PET; YP-GSHN-2013_PIN; YP-GSHN-2013_PO1; YP-GSHN-2013_PO2; YP-GSHN-2013_QUE; YP-GSHN-2013_ROS; YP-GSHN-2013_SAB; YP-GSHN-2013_SAC; YP-GSHN-2013_SAL; YP-GSHN-2013_SEN; YP-GSHN-2013_SEP; YP-GSHN-2013_SIJ; YP-GSHN-2013_SIL; YP-GSHN-2013_TEK; YP-GSHN-2013_TIC; YP-GSHN-2013_VAL; YP-GSHN-2013_VER; YP-GSHN-2013_YAL; YP-GSHN-2013_YAX; YP-GSHN-2013_YOJ; YP-GSHN-2013_YUM
    Type: Dataset
    Format: text/tab-separated-values, 1652 data points
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