As operárias de abelhas sem ferrão são peculiares com relação à divisão do trabalho reprodutivo para a manutenção da colônia, visto que podem produzir ovos reprodutivos que originam os machos, além dos ovos tróficos destinados a alimentar a rainha. Desta forma, os estudos de expressão de genes e de proteínas envolvidos na biossíntese de vitelo vitelogênese - e incorporação deste material aos ovócitos contribuem para evidenciar diferenças intra e inter-específicas entre as fêmeas, em relação à fertilidade e comportamento reprodutivo. Os perfis de expressão do gene codificador da vitelogenina e da própria proteína, precursora da principal constituinte do vitelo, foram determinados para várias etapas do desenvolvimento de três espécies de abelhas sem ferrão. Para este estudo foram selecionadas as espécies Frieseomelitta varia, cujas operárias nunca põem ovos, mesmo em condições de orfandade, Scaptotrigona postica e Melipona scutellaris, cujas operárias desenvolvem os ovários e participam ativamente da produção de machos. O RNA total de corpo gorduroso sítio de biossíntese de vitelogenina de operárias destas espécies foi extraído e o cDNA obtido por transcrição reversa semiquantitativa foi amplificado, clonado e seqüenciado utilizando-se primers específicos para a vitelogenina de Apis mellifera. Os resultados revelaram que os cDNA parciais obtidos são bastante conservados entre F. varia, S. postica e M. scutellaris e mostram alta identidade (93-100%) em relação à região 3-terminal do cDNA da vitelogenina de A. mellifera. Entretanto, o perfil de abundância do transcrito difere entre as espécies de meliponíneos e entre estas e as abelhas melíferas. Em F. varia e S. postica a expressão do transcrito mostrou-se constitutiva ao longo dos períodos pupal e adulto, mas M. scutellaris mostrou diminuição da abundância de transcritos nas fases pupais mais avançadas e nas operárias recém-emergidas. Estas espécies diferem de A. mellifera cujas pupas não expressam o gene da vitelogenina. A expressão constitutiva deste gene em F. varia e S. postica mostra que a atividade do gene em questão não é modificada pela variação dos títulos de ecdisteróides e hormônio juvenil descrita para A. mellifera e outros insetos, indicando, portanto, ausência de controle da transcrição de vitelogenina por hormônios nas espécies de meliponíneos estudadas. No entanto, os resultados indicam a existência de controle nutricional da atividade do gene da vitelogenina, dado o aumento de expressão verificado em operárias F. varia alimentadas com dieta rica em proteínas (contendo pólen - a fonte de proteínas para as abelhas - e açúcar) em comparação com aquelas que receberam dieta exclusiva de carboidrato (açúcar). A presença da proteína vitelogenina na hemolinfa de F. varia ocorre concomitantemente com a expressão constitutiva do transcrito. Neste aspecto, difere de S. postica e M. scutellaris que também expressam o transcrito da vitelogenina ao longo do estágio pupal e adulto, mas a proteína correspondente somente é detectada nas operárias destas espécies que estão exercendo a função de nutridoras de crias. Pode-se concluir que o gene da vitelogenina é conservado entre as espécies de abelhas até aqui estudadas, porém sua expressão e possivelmente sua regulação diferem entre meliponíneos e abelhas melíferas, refletindo as diferentes estratégias utilizadas na divisão do trabalho reprodutivo. / The stingless bee workers are peculiar with relation to reproductive division of labor to colony maintenance, since they are able to produce reproductive eggs that will develop in males, beyond trophic eggs to feed the queen. In this way, studies about gene and protein expression involved on the yolk biosynthesis vitellogenesis and the incorporation of this material to the oocytes contributes to evidence intra and inter-specific differences between females, in relation to fertility and reproductive behavior. The vitellogenin, the main yolk constituent precursor, gene expression and the protein itself profile were determined to several developmental stages of three stinglessbee species. To this work were selected the species Frieseomelitta varia, whose workers never lay eggs, even in a queenless condition, Scaptotrigona postica and Melipona scutellaris, whose workers develop their ovaries and participate actively to male production. The whole RNA of the fat body the vitellogenin biosynthesis site - of these worker species was extracted and the cDNA obtained by semiquantitative reverse transcription amplified, cloned and sequenced through Apis mellifera vitellogenin specific primers. The results reveal that the obtained partial cDNAs are very conserved among F. varia, S. postica and M. scutellaris and show high identity (93-100%), in relation to 3-end A. mellifera vitellogenin gene. However, transcript abundance profile is different among stinglessbee species and with honeybees. In F. varia and S. postica the transcript expression is constitutive during pupal and adult periods, but M. scutellaris showed transcript reduction in the advanced pupal phases and newly emerged workers. These species are different from A. mellifera pupae that do not express vitellogenin gene. This constitutive gene expression in F. varia and S. postica shows that the gene activity is not modified by the ecdysteroid and juvenile hormone titers as descript to A. mellifera and other insects, indicating absence of vitellogenin transcriptional control by hormones in the studied stingless bee species. However, the results indicate the existence of vitellogenin gene activity nutritional control, given the verified expression increase in F. varia workers and drones fed with a rich protein diet (with pólen the protein bee source and sugar) in comparison with which ones received exclusive sugar diet. The presence of vitellogenin protein on the F. varia hemolimph occurs concomitantly with the constitutive transcript expression. In this aspect, is different of S. postica and M. scutellaris which also express the vitellogenin transcript during pupal and adult stages, but the correspondent protein is only detected on the workers of these species that are exerting nurse tasks. Is possible conclude that vitellogenin gene is conserved among the studied bee species, but its expression and possibly regulation are different among stingless bees and honey bees, reflecting different strategies used on reproductive division of labor.

The Crimson-spotted rainbowfish (Melanotaenia fluviatilis) from the Murray-Darling basin of Australia is a common indicator species in Australian ecotoxicology. Biochemical changes have been investigated in this species, but not molecular markers of ecotoxicological interest. In this study genes of M. fluviatilis were isolated using a cDNA library and sequences analysed. Of 345 randomly selected clones, 94 shared similarity with 26 different genes in other organisms in public databases. Amongst these, reproductive genes coding for vitellogenin, retinol binding protein, sialyltransferase and zona pellucida protein were considered of interest in ecotoxicology. The vitellogenin gene was selected for study as it has been widely used as a molecular marker of exposure to 17â-estradiol (E2) in teleosts. Gene expression was examined via northern blot, RT-PCR and Real-Time PCR relative to the housekeeping gene (18S rRNA). The expression of vitellogenin mRNA was observed a t 12 hours post-exposure, peaked at 48 hours according to northern blot analysis; and cleared within 4 days, partly consistent with RT-PCR. However, Real-time PCR yielded an inconclusive result, probably due to differences between pooled and individual samples. Vitellogenin in blood plasma was confirmed by western blot, found to be significantly increased and retained in the plasma in fish treated with E2 compared to controls. It was concluded that vitellogenin mRNA is a molecular marker of exposure to 17â-estradiol in the rainbowfish, and could potentially be used as a marker of exposure to environmental estrogenic chemicals. Further investigations of the expression of genes in the cDNA library, could establish other molecular markers of ecotoxicological interest in M. fluviatilis.

Receptors that transport vitellogenin into oocytes are of vital importance to egg-laying species because they promote oocyte development. In this study, we describe the cloning of the first hymenopteran vitellogenin receptor (VgR) cDNA. Using reverse transcription polymerase chain reaction (RT-PCR) and both 5’- and 3’- rapid amplification of cDNA ends (RACE), cDNA fragments encompassing the entire coding region of a putative VgR from fire ant (= SiVgR) were cloned and sequenced. The complete SiVgR cDNA has a length of 5764 bp encoding a 1782-residue protein with a predicted molecular mass of 201.3 kDa. The deduced amino acid sequence of the SiVgR revealed that it encoded a protein belonging to the low-density lipoprotein receptor superfamily. The number and arrangement of modular domains of SiVgR are the same as those of mosquito and fruit fly VgRs, except there are only four Class A cysteine-rich repeats in the first ligand binding domain of SiVgR compared to five in the mosquito and fruit fly. The deduced amino acid sequence of the SiVgR exhibited 35% and 31% identity to those of the mosquito and fruit fly VgRs, respectively. Northern blot analysis demonstrated that the 7.4-kb SiVgR mRNA was present only in Northern blot analysis demonstrated that the 7.4-kb SiVgR mRNA was present only in ovaries of reproductive females − both alates (virgins) and queens (mated) and was more abundant in alates. The developmental profile of transcriptional expression was determined by semiquantitative RT-PCR. It showed that the SiVgR transcript increased 6-fold from 0- to 10-days after mating, then remained constant through 30 days. It also showed that the SiVgR transcripts increased with age in alate virgin females. The transcriptional expression of the SiVgR was up-regulated more than two-fold by methoprene, a juvenile hormone analog, as determined by using an in vitro system. This suggested the SiVgR gene is JH regulated.

Receptors that transport vitellogenin into oocytes are of vital importance to egg-laying species because they promote oocyte development. In this study, we describe the cloning of the first hymenopteran vitellogenin receptor (VgR) cDNA. Using reverse transcription polymerase chain reaction (RT-PCR) and both 5’- and 3’- rapid amplification of cDNA ends (RACE), cDNA fragments encompassing the entire coding region of a putative VgR from fire ant (= SiVgR) were cloned and sequenced. The complete SiVgR cDNA has a length of 5764 bp encoding a 1782-residue protein with a predicted molecular mass of 201.3 kDa. The deduced amino acid sequence of the SiVgR revealed that it encoded a protein belonging to the low-density lipoprotein receptor superfamily. The number and arrangement of modular domains of SiVgR are the same as those of mosquito and fruit fly VgRs, except there are only four Class A cysteine-rich repeats in the first ligand binding domain of SiVgR compared to five in the mosquito and fruit fly. The deduced amino acid sequence of the SiVgR exhibited 35% and 31% identity to those of the mosquito and fruit fly VgRs, respectively. Northern blot analysis demonstrated that the 7.4-kb SiVgR mRNA was present only in Northern blot analysis demonstrated that the 7.4-kb SiVgR mRNA was present only in ovaries of reproductive females − both alates (virgins) and queens (mated) and was more abundant in alates. The developmental profile of transcriptional expression was determined by semiquantitative RT-PCR. It showed that the SiVgR transcript increased 6-fold from 0- to 10-days after mating, then remained constant through 30 days. It also showed that the SiVgR transcripts increased with age in alate virgin females. The transcriptional expression of the SiVgR was up-regulated more than two-fold by methoprene, a juvenile hormone analog, as determined by using an in vitro system. This suggested the SiVgR gene is JH regulated.

Municipal wastewater treatment plants (MWWTPs) are point sources of environmental contamination that can cause adverse effects on fish species exposed to their effluents (MWWEs). Contaminants, such as endocrine disrupting compounds (EDCs), commonly found in MWWEs have been shown to induce many adverse reproductive effects. In the Grand River watershed of southern Ontario, three MWWTPs from the cities of Guelph, Waterloo and Kitchener have been identified to adversely alter molecular and cellular responses in fish, which have been previously associated with exposure to estrogenic EDCs. Currently these systems are undergoing process upgrades to address aging infrastructure as well as expanding capacities to serve rapidly increasing populations. Studies in this thesis were conducted to determine whether the Guelph and Waterloo MWWEs, as well as surrogate pilot plant effluents that modeled possible treatment process upgrades for MWWTPs were estrogenic in vivo in controlled laboratory exposures. Unfortunately, the Kitchener MWWE (conventional activated sludge and lagoon) was acutely toxic and could not be included in laboratory exposures. Rainbow trout (Oncorhynchus mykiss) were exposed to 20% to 90% effluent from both Guelph and Waterloo, for 2, 8 and 14 days and fish plasma was analyzed for vitellogenin (VTG) a biomarker for estrogenic exposure. These exposures indicated that neither the Guelph nor the Waterloo MWWE were estrogenic in vivo under the exposure conditions in this study. In contrast the total estrogenic equivalence measured using the yeast estrogen screen (YES) of the Guelph, Waterloo and Kitchener MWWEs increased respectively, inversely related to the degree of treatment. Three pilot plant effluents (Burlington MWWTP) including conventional activated sludge (CAS), nitrifying with CAS (CAS-N) and biological nutrient removal with CAS (CAS-BNR) were also tested in rainbow trout in vivo for plasma VTG induction. Only the CAS-BNR effluent caused weak (2-3.5 fold) induction of VTG relative to controls. Although the estrogenicity (YES) of the effluent was variable the VTG induction corresponded with the slightly higher 17??-estradiol equivalents measured in these pilot plant effluents. An effect-directed analysis (EDA) for estrogenic substances was carried out on the Waterloo and Kitchener MWWEs and revealed that the estrogenicity (YES) of the Waterloo MWWE was associated with estrone, while the estrogenicity of the Kitchener MWWE was associated with several chemicals (estrone > 17??-estradiol > bisphenol A ~ testosterone).

Endocrine disrupting compounds (EDC) are environmental contaminants that disrupt reproduction, development and behaviour in aquatic organisms. A thorough evaluation of the impacts of EDCs on aquatic organisms is currently limited by a lack of robust biomarkers in small model fish, particularly for assessing EDCs with (anti-)androgenic activity. Male sticklebacks build nests using spiggin, an androgen-responsive glycoprotein, which can be used to assess (anti-)androgenic exposure. EDC assessment in the field using threespine stickleback and the spiggin biomarker is limited to coastal and estuarine environments. However, their freshwater relative, brook stickleback (Culaea inconstans), also possess spiggin and their widespread distribution suggests that they may have applications as a bioindicator of EDCs in freshwater systems. Therefore, the overall objective of this thesis was to determine if brook stickleback are a suitable bioindicator species for EDCs by evaluating their response and sensitivity to estrogenic and (anti-)androgenic chemicals. Basal transcript levels of spiggin in kidney and vitellogenin in liver were first measured in wild-caught brook stickleback using qPCR and found to be differentially expressed in males and females. Brook stickleback were then exposed to two model compounds, 17α-ethinylestradiol (EE2) and 17α-methyltestosterone (MT), at 1, 10 and 100 ng/L for 21 days (sampled at 7 and 21 days) via static-renewal to determine the responsiveness of these transcripts to exogenous hormones. The effect of hormone exposure on condition factor, organosomatic indices and histopathology of kidneys was also measured. Exposure to MT and EE2 significantly induced spiggin and vitellogenin transcripts in female kidneys and male livers, respectively. Exposure to EE2 also significantly increased the hepatosomatic index in females after 7 days and in both sexes after 21 days whereas the gonadosomatic index was reduced in females after 21 days. An increase in kidney epithelium cell height was also observed in MT-exposed females and males after 7 days. These results mirror those of threespine stickleback and suggest that brook stickleback are responsive to androgenic and estrogenic chemical exposure and more specifically, possess quantifiable and sensitive biomarkers for exposure to compounds with androgenic activity. In a third experiment, female fish were co-exposed to MT at 500 ng/L and an anti-androgen (flutamide; FL) at 25, 150 and 250 µg/L for 14 days (sampled at 4 and 14 days) to validate this bioassay for the evaluation of anti-androgens using the same endpoints as in the previous two experiments. In females, exposure to MT increased spiggin transcript levels and nephrosomatic index (NSI) but co-exposure to FL did not result in a significant suppression of these endpoints because of high inter-individual variability. In males, exposure to MT increased NSI and co-exposure to FL resulted in a reduction in this endpoint, illustrating anti-androgenic effects. Although the response of brook stickleback to hormone exposure was endpoint-specific and was at times lower than other small model fish species, the ability to simultaneously assess estrogenic and (anti-)androgenic chemical exposure in a single fish using quantitative endpoints is an advantage exclusively held by members of the stickleback family. The results of this thesis suggest that brook stickleback hold promise as an additional small fish model for the evaluation of EDCs, with potential application in EDC biomonitoring in the freshwaters of North America.

As operárias de abelhas sem ferrão são peculiares com relação à divisão do trabalho reprodutivo para a manutenção da colônia, visto que podem produzir ovos reprodutivos que originam os machos, além dos ovos tróficos destinados a alimentar a rainha. Desta forma, os estudos de expressão de genes e de proteínas envolvidos na biossíntese de vitelo vitelogênese - e incorporação deste material aos ovócitos contribuem para evidenciar diferenças intra e inter-específicas entre as fêmeas, em relação à fertilidade e comportamento reprodutivo. Os perfis de expressão do gene codificador da vitelogenina e da própria proteína, precursora da principal constituinte do vitelo, foram determinados para várias etapas do desenvolvimento de três espécies de abelhas sem ferrão. Para este estudo foram selecionadas as espécies Frieseomelitta varia, cujas operárias nunca põem ovos, mesmo em condições de orfandade, Scaptotrigona postica e Melipona scutellaris, cujas operárias desenvolvem os ovários e participam ativamente da produção de machos. O RNA total de corpo gorduroso sítio de biossíntese de vitelogenina de operárias destas espécies foi extraído e o cDNA obtido por transcrição reversa semiquantitativa foi amplificado, clonado e seqüenciado utilizando-se primers específicos para a vitelogenina de Apis mellifera. Os resultados revelaram que os cDNA parciais obtidos são bastante conservados entre F. varia, S. postica e M. scutellaris e mostram alta identidade (93-100%) em relação à região 3-terminal do cDNA da vitelogenina de A. mellifera. Entretanto, o perfil de abundância do transcrito difere entre as espécies de meliponíneos e entre estas e as abelhas melíferas. Em F. varia e S. postica a expressão do transcrito mostrou-se constitutiva ao longo dos períodos pupal e adulto, mas M. scutellaris mostrou diminuição da abundância de transcritos nas fases pupais mais avançadas e nas operárias recém-emergidas. Estas espécies diferem de A. mellifera cujas pupas não expressam o gene da vitelogenina. A expressão constitutiva deste gene em F. varia e S. postica mostra que a atividade do gene em questão não é modificada pela variação dos títulos de ecdisteróides e hormônio juvenil descrita para A. mellifera e outros insetos, indicando, portanto, ausência de controle da transcrição de vitelogenina por hormônios nas espécies de meliponíneos estudadas. No entanto, os resultados indicam a existência de controle nutricional da atividade do gene da vitelogenina, dado o aumento de expressão verificado em operárias F. varia alimentadas com dieta rica em proteínas (contendo pólen - a fonte de proteínas para as abelhas - e açúcar) em comparação com aquelas que receberam dieta exclusiva de carboidrato (açúcar). A presença da proteína vitelogenina na hemolinfa de F. varia ocorre concomitantemente com a expressão constitutiva do transcrito. Neste aspecto, difere de S. postica e M. scutellaris que também expressam o transcrito da vitelogenina ao longo do estágio pupal e adulto, mas a proteína correspondente somente é detectada nas operárias destas espécies que estão exercendo a função de nutridoras de crias. Pode-se concluir que o gene da vitelogenina é conservado entre as espécies de abelhas até aqui estudadas, porém sua expressão e possivelmente sua regulação diferem entre meliponíneos e abelhas melíferas, refletindo as diferentes estratégias utilizadas na divisão do trabalho reprodutivo. / The stingless bee workers are peculiar with relation to reproductive division of labor to colony maintenance, since they are able to produce reproductive eggs that will develop in males, beyond trophic eggs to feed the queen. In this way, studies about gene and protein expression involved on the yolk biosynthesis vitellogenesis and the incorporation of this material to the oocytes contributes to evidence intra and inter-specific differences between females, in relation to fertility and reproductive behavior. The vitellogenin, the main yolk constituent precursor, gene expression and the protein itself profile were determined to several developmental stages of three stinglessbee species. To this work were selected the species Frieseomelitta varia, whose workers never lay eggs, even in a queenless condition, Scaptotrigona postica and Melipona scutellaris, whose workers develop their ovaries and participate actively to male production. The whole RNA of the fat body the vitellogenin biosynthesis site - of these worker species was extracted and the cDNA obtained by semiquantitative reverse transcription amplified, cloned and sequenced through Apis mellifera vitellogenin specific primers. The results reveal that the obtained partial cDNAs are very conserved among F. varia, S. postica and M. scutellaris and show high identity (93-100%), in relation to 3-end A. mellifera vitellogenin gene. However, transcript abundance profile is different among stinglessbee species and with honeybees. In F. varia and S. postica the transcript expression is constitutive during pupal and adult periods, but M. scutellaris showed transcript reduction in the advanced pupal phases and newly emerged workers. These species are different from A. mellifera pupae that do not express vitellogenin gene. This constitutive gene expression in F. varia and S. postica shows that the gene activity is not modified by the ecdysteroid and juvenile hormone titers as descript to A. mellifera and other insects, indicating absence of vitellogenin transcriptional control by hormones in the studied stingless bee species. However, the results indicate the existence of vitellogenin gene activity nutritional control, given the verified expression increase in F. varia workers and drones fed with a rich protein diet (with pólen the protein bee source and sugar) in comparison with which ones received exclusive sugar diet. The presence of vitellogenin protein on the F. varia hemolimph occurs concomitantly with the constitutive transcript expression. In this aspect, is different of S. postica and M. scutellaris which also express the vitellogenin transcript during pupal and adult stages, but the correspondent protein is only detected on the workers of these species that are exerting nurse tasks. Is possible conclude that vitellogenin gene is conserved among the studied bee species, but its expression and possibly regulation are different among stingless bees and honey bees, reflecting different strategies used on reproductive division of labor.

abstract: Vitellogenin (Vg) is an ancient and highly conserved multifunctional protein. It is primarily known for its role in egg-yolk formation but also serves functions pertaining to immunity, longevity, nutrient storage, and oxidative stress relief. In the honey bee (Apis mellifera), Vg has evolved still further to include important social functions that are critical to the maintenance and proliferation of colonies. Here, Vg is used to synthesize royal jelly, a glandular secretion produced by a subset of the worker caste that is fed to the queen and young larvae and which is essential for caste development and social immunity. Moreover, Vg in the worker caste sets the pace of their behavioral development as they transition between different tasks throughout their life. In this dissertation, I make several new discoveries about Vg functionality. First, I uncover a colony-level immune pathway in bees that uses royal jelly as a vehicle to transfer pathogen fragments between nestmates. Second, I show that Vg is localized and expressed in the honey bee digestive tract and suggest possible immunological functions it may be performing there. Finally, I show that Vg enters to nucleus and binds to deoxyribonucleic acid (DNA), acting as a potential transcription factor to regulate expression of many genes pertaining to behavior, metabolism, and signal transduction pathways. These findings represent a significant advance in the understanding of Vg functionality and honey bee biology, and set the stage for many future avenues of research. / Dissertation/Thesis / Doctoral Dissertation Evolutionary Biology 2019

The Assabet River located in eastern Massachusetts receives treated wastewater discharges from four major municipal wastewater treatment plants (WWTPs): Westborough, Marlborough, Hudson and Maynard. In periods of low flow, up to 95% of the Assabet River is wastewater effluent. Chemical analyses have shown that municipal wastewaters can contain estrogenic and dioxin-like compounds. Estrogenic compounds such as the natural estrogen 17β-estradiol (E2), the synthetic estrogen 17α-ethinyl estradiol (EE2), and the industrial compound nonylphenol (NP) can induce vitellogenin (VTG) and lead to feminization in male fish. CYP1A1-inducing compounds such as the polycyclic aromatic hydrocarbons (PAHs) and polybrominated diphenyl ethers (PBDEs) can produce both overt toxicity and alter reproductive function through the metabolism of natural estrogens. The purpose of the present research is to analyze the estrogenic and CYP1A1-inducing compounds in the Assabet River and their physiological effects on Japanese Medaka (Oryzias latipes). I used a bioassay that measures the induction of VTG and CYP1A1 in the livers of male Medaka and report results obtained by the USGS and EPA on analytical measurements of selected compounds. In the summers of 2010 and 2011 water samples were collected from the Assabet River, its tributaries and the four WWTPs. Male Medaka were exposed to the treatment samples as well as negative and positive controls. VTG and CYP1A1 induction were measured using real time RT-PCR. Concurrently collected samples from 2010 were analyzed by the USGS for more than 80 organic wastewater contaminants including several estrogenic EDCs and CYP1A1-inducing compounds. The USEPA also analyzed treated wastewater effluent samples collected from the four WWTPs for pharmaceuticals, hormones, nonylphenols and perfluorinated compounds. The bioassay from 2010 and 2011 reveal no statistically significant induction of VTG expression and only one significant induction of CYP1A1 expression. Few compounds were detected by the 2010 USGS and USEPA chemical analyses and the concentrations were low. Taken together the results indicate that VTG and CYP1A1 inducing compounds in the effluent-dominated Assabet River are present at low levels, which may be below the level of detection of the bioassays. In addition to the biological assay and chemical analysis Geographic Information Systems (GIS) was used to analyze land use/land cover (LU/LC) data in the Assabet River Watershed. Much of the land surrounding the Assabet River is forested but there are several LU/LC types that could negatively impact the water quality. High impact and low impact LU/LC types were differentiated in buffers around the Assabet River and six GIS sites. The composition of each site varies widely in its proportions of high and low impact land cover. The GIS analysis established locations on the Assabet River where water quality is more susceptible to degradation due to the distribution of high impact land use types.

Teleosts are one of the most diverse groups of vertebrates. They utilize a wide array of reproductive strategies and tactics to overcome the challenges of the many ecological niches they inhabit. The most common reproductive method for teleosts is oviparity. Oviparous animals lay eggs with little or no embryonic development from the mother. The embryos are supplied with nutrition via yolk. Vitellogenesis is the process of the ovary sequestering yolk. It is regulated by exogenous environmental cues that act on the hypothalamus-pituitary-gonad axis. Through a series of hormonal controls, the liver produces the yolk precursor, vitellogenin. Vitellogenin is secreted by the liver and absorbed by the growing oocyte by receptor mediated endocytosis. There it is cleaved into the two main yolk proteins which are subsequently used by the growing embryo. The biggest source of nutrition is the yolk protein lipovitellin which also plays a key role in marine teleosts’ ability to osmoregulate their eggs. Lipovitellin is a large glyco-phospho-lipo-protein ca. 200 kDa. Large proteins usually denature easily. However, prior evidence shows that fish lipovitellins are thermally stable. Using differential scanning calorimetry, I quantify lipovitellin’s thermostability amongst four right-eye flounders (Pleuronectidae: winter flounder, American plaice, witch flounder, and yellowtail flounder). Differential scanning calorimetry allows direct interpretation of all thermodynamic properties; however, Lipovitellin was too large and precipitated before other thermodynamic properties could be determined. Pleuronectid lipovitellins all showed high melting points indicative of high thermostability. This shows that despite differing life histories, lipovitellin is conserved. Presence of the pre-cursor, vitellogenin in male or juvenile fish is used as a biomarker for xenoestrogens, a type of endocrine disrupting chemicals that blocks or mimics natural estrogens. They are known to disrupt aquatic life by interfering with natural development and reproduction. A major biological side effect of xenoestrogens is the accumulation of vitellogenin. This effect has made vitellogenin a useful biomarker for monitoring levels of contamination. Unfortunately, vitellogenin can vary greatly in its immunological and structural characteristics, which means that species-specific assays are necessary. This study took the first step in developing an immunoassay for bluefish (Pomatomus saltatrix). Vitellogenin was induced by injecting a group of bluefish with an estrogen, estradiol, and the resulting vitellogenin was isolated from the serum of males. The protein was characterized as vitellogenin by determining its large Stokes radius in gel permeation chromatography combined with its characteristic peptide molecular weight in sodium dodecyl sulfate polyacrylamide gel electrophoresis.